Magic Medicine by Cody Johnson
Magic Medicine by Cody Johnson
Magic Medicine by Cody Johnson
INTRODUCTION
1 CLASSICAL PSYCHEDELICS
2C-B AND THE 2C FAMILY
5-MEO-DMT
AYAHUASCA
DMT
DOM AND THE DOX FAMILY
LSD
MORNING GLORY
PEYOTE
PSILOCYBIN MUSHROOMS
SAN PEDRO
YOPO AND VILCA BEANS
2 EMPATHOGENIC PSYCHEDELICS
MDA
MDMA
3 DISSOCIATIVE PSYCHEDELICS
DXM
KETAMINE
NITROUS OXIDE
SALVIA
4 UNIQUE PSYCHEDELICS
AMANITA MUSCARIA
CANNABIS
DIPT
FISH AND SEA SPONGES
IBOGA
MAD HONEY
ACKNOWLEDGMENTS
ABOUT THE AUTHOR
REFERENCES
INDEX
A PEEK INTO THE FUTURE
OF
PSYCHEDELIC MEDICINE
It’s Tuesday morning, and you wander into your local Psychedelic
Clinic. At the front desk they take your name: “Yes,” says the
receptionist, “we’re expecting you. Right this way.” You’re whisked
into a comfortable room where an open window bathes a wall of
bookshelves in yellow light.
The therapist enters, but looks more like a neighborly professor—
horn-rim glasses, brown vest, a pair of loafers. “Have a seat,” he
says, nodding toward a cozy-looking couch. He hands you a glass of
water and a small pill containing 150 milligrams of pure MDMA
(Ecstasy). You take it and lean back. The session begins.
CLASSICAL PSYCHEDELICS
From time-honored shamanic tools to brand new molecular
inventions, the classical psychedelics elicit their effects by tickling the
brain’s serotonin system. Including such iconic substances as LSD,
psilocybin mushrooms, and peyote cacti, this collection defines what
it means to be psychedelic.
2C-B AND THE 2C FAMILY
DISCOVERED DURATION
Alexander Shulgin in 1974 Varies widely
ASSOCIATED WITH underground psychotherapy and the modern psychedelic scene
FIG. 1.1
2-(4-BROMO-2,5-DIMETHOXYPHENYL) ETHYLAMINE
T decades and has touched the lives of many thousands. What began as an
offhand experiment by an eccentric chemist would soon yield some of the
most significant psychedelic molecules of the modern era.
When the eminent psychedelic chemist Alexander Shulgin and his colleague
Michael Carter debuted 2C-B in 1975, they could not have known the beast they
were unleashing. This chemical would spawn a series of related compounds
whose merits and shortcomings would be hotly discussed by chemists,
therapists, and consciousness explorers for decades.
Whether on a rave dance floor or the therapist’s couch, 2C-B and its ilk
spelled upheaval. Agents of change are always feared, however, and it’s no
surprise most of these compounds were soon outlawed in many countries—even
though their therapeutic potential appeared to outweigh their relatively low
toxicity. Once widely available in Amsterdam head shops and online
marketplaces, most of the 2C compounds are now relegated to the black market.
Members of the 2C series count among Shulgin’s most popular creations,
including the lucid aphrodisiac 2C-B. He was especially proud of them, and, by
most accounts, rightfully so.
[ WHAT’S IN A NAME? ]
In the early 1970s, Shulgin was experimenting with DOB, an “extremely potent
and long-lived” psychedelic amphetamine he’d found seven years earlier, when
he discovered the 2C series. Shulgin realized that, with a single tweak, every
member of the “DOx” family could yield a potent 2C derivative. And voilà—a
whole new series of chemicals was born, each with its own psychoactive profile.
To name each new compound, Shulgin used the final letter of its prototype:
2C-B is based on DOB, 2C-I is based on DOI, and so on. All the 2C chemicals
are identical to their namesakes, except for that one inspired tweak first made by
a chemical wizard back in the 1970s.
2C-B has earned praise as a superlative psychedelic, frequently mentioned in the same breath as
mescaline and LSD.
[ THE EXPERIENCE ]
Of all of Shulgin’s inventions, 2C-B stands apart. The first and most famous of
the 2Cs, it has earned praise as a superlative psychedelic, frequently mentioned
in the same breath as mescaline and LSD. Lucid, gentle, and even erotic, 2C-B
has been celebrated by generations of psychonauts for its aesthetic beauty and
manageability. A remarkably flexible compound, it is easily molded to the user’s
intentions, especially at low to moderate doses.
Where some psychedelics can be extremely stimulating and tie the tongue
into knots, 2C-B is relatively calm and leaves one’s communication faculties
largely intact. When someone is teetering on the precipice of a drug-induced
mental crisis, grasping at any rope that leads back to reality, the ability to
communicate can mean the difference between momentary anxiety and a full-
fledged freak-out. Among the mildest and shortest of psychedelic experiences,
2C-B often serves as a tripper’s first encounter with psychedelics.
Shulgin considered 2C-B his favorite of all substances. He took it often,
referring to it as the “Great Teacher.” Perhaps more than any other drug, 2C-B
has been celebrated for its sensual nature. One of Shulgin’s testers gave this
report:
In a 2003 column for the Center for Cognitive Liberty & Ethics, Sasha
extolled 2C-B’s virtues as:
[ A BROAD APPEAL ]
Indeed, 2C-B originally gained popularity among therapists and their patients
who found the compound very effective at fostering compassionate relationships
and bringing traumas and insecurities to light in a nonthreatening way. As with
MDMA, however, word got out and 2C-B quickly expanded beyond its
therapeutic roots. The compound invaded dance floors and bedrooms as it gained
renown as a tactile, emotional, and sexual enhancer. During its legal heyday, a
German company even marketed it as an aphrodisiac called Erox.
Dutch “smart shops” also sold 2C-B as an Ecstasy-like legal high under the
name “Nexus.” That moniker is still used occasionally, and it’s especially fitting
for a substance at the intersection of so many interests and disciplines. From
chemistry and psychiatry to music and romance, 2C-B crosses many paths.
When politics and law enforcement joined the ranks of those interested in 2C-
B, its days as a legal high were numbered. The United States banned it in 1995;
by 2000, it was prohibited around the world.
By meaning many things to many people, 2C-B illuminates the arbitrary
nature of our labels for drugs. Where therapists saw a remarkable new medicine,
couples found a powerful aphrodisiac and young ravers found a hip new flavor
of consciousness to tap into. Meanwhile, law enforcement agencies and many
well-meaning but poorly informed citizens—egged on by sensational media
reports and decades of antidrug propaganda—saw, and continue to see, only a
dangerous club drug. 2C-B is all of these, and yet none. The molecule remains
the same; only our approach to it changes.
FIG. 1.2
5-METHOXY-N,N-DIMETHYLTRYPTAMINE
[ ORIGINS AND BACKGROUND ]
-MEO-DMT IS AS DIVERSE AND ENIGMATIC AS ONE substance can be. It is one of
5 humanity’s oldest sacraments, yet one of our newest discoveries. It provides
an overwhelming, profound, and sacred experience, yet it is used casually by
men of the Yanomami tribes on a daily basis. It is both rare and exceptionally
common—though it occurs naturally in dozens of plants and animals, including
humans, the chemical remains obscure and is rarely encountered on the
underground drug market. And it is both organic and synthetic—once the
exclusive product of nature, concentrated in especially high quantities in the bark
of certain jungle trees, it is now easily manufactured in labs around the world.
The bow on this package of paradoxes was tied in 1965, when high levels of
5-MeO-DMT were identified in the venom of the Colorado River Toad. This
discovery holds more significance than it sounds—although the plant world
teems with psychedelic molecules, animals with high quantities of such
substances are practically unheard of. The toad appears to be unique, though
many of its relatives in the Bufo genus produce bufotenine, only the Colorado
River Toad, Bufo alvarius, bears an enzyme that converts it into plentiful 5-
MeO-DMT.
Some people have taken to “milking” the venom from the toads’ parotid
glands and vaporizing it for psychedelic effects. Animal lovers may take some
solace: This is said to be painless, involving nothing more than a glass slide
rubbed against the toad’s glands to collect the goo. In some areas, however, the
toad is classified as a threatened species and may not be removed from its habitat
legally. Some media outlets have sensationalized “toad licking” as a new
phenomenon, but these reports are probably exaggerated if not outright false.
Because the venom contains other toxins, which appear to be destroyed by heat
when vaporized, leaving only the desired compounds intact—direct consumption
by licking is ill advised. As bizarre as it sounds, smoking toad venom marks a
pioneering step for humanity: Along with “mad” honey and certain species of
visionary fish, it is one of the only psychedelic experiences sourced from
animals.
[ CLOSER TO HOME ]
5-MeO-DMT is not just an elusive jungle potion, limited to a few shamans and
adventurous toad smokers. Within ten years of the toad discovery, science threw
another curveball: several studies confirmed the existence of 5-MeO-DMT in
human tissues. It is still one of only two known “endogenous” entheogens—
psychedelics produced naturally by the human body. The other is N,N-DMT—
often shortened to DMT—and the exact function of both remains a mystery.
Once considered exotic and obscure, 5-MeO-DMT turns out to be
surprisingly widespread: Every one of us is a walking supply closet. This leads
to a few awkward questions—as DMT and 5-MeO-DMT are illegal, does that
make our bodies contraband? Technically, yes. Legislators haven’t bothered to
address that conundrum, and, until they do, you could, within the letter of the
law, be booked for possession of a controlled substance. Someone needs to bring
attention to this loophole, but the airport security line is probably not the best
place to do it.
[ THE EXPERIENCE ]
5-MeO-DMT may be little known outside select circles, but it packs a punch that
far exceeds its small reputation. Structurally related to DMT—often considered
the most powerful of all psychedelics—the 5-MeO variant is said to be even
more overwhelming. Proponents insist its ability to launch users to a spiritual
state of oneness is unparalleled. Wade Davis, an anthropologist who studied the
Yanomami people, compared the epená snuff ritual to “being shot out of a rifle
barrel lined with Baroque paintings and landing on a sea of electricity.”
Its intensity is matched by its potency—at roughly five times the strength of
DMT, you certainly would not want to confuse the two. When vaporized, it is
active as low as 2 milligrams; 10 milligrams is enough to skyrocket most people
to another dimension. As one user writes: “If most hallucinogens, including
LSD, merely distort reality, however bizarrely, 5-MeO-DMT completely
dissolves reality as we know it, leaving neither hallucinations nor anyone to
watch them. The experience… is not for the novice.”
Users often believe they have died and passed into the afterlife, shedding their human identities as
they enter the light.
The effects are said to be ineffable, but that hasn’t stopped countless explorers
from attempting to describe them. As with DMT, online “trip reports” often
mention its sudden and extreme intensity, with the onset likened to the blastoff
of a rocket ship. Both substances are described as profound, bewildering, and
utterly alien to everyday consciousness, with sought-after spiritual states often
going hand in hand with moments of primal fear.
That may be where the similarities end. Unlike DMT, famous for its swirling,
intricate geometric patterns and mind-bending alien landscapes, 5-MeO-DMT is
not especially visual in nature. Psychedelic aficionados are divided. Some prefer
the purity of 5-MeO-DMT, which offers a full spiritual experience without the
visual distractions, while others prefer the vibrant, interactive world of DMT and
find its 5-MeO variant cold and colorless.
Undoubtedly, it’s a substance for serious exploration, not recreation. Many
even consider it sacred, as the Yanomami do. Terms such as “oneness,” “white
light,” “pure love,” and “ego loss” may sound cribbed from descriptions of
religious ecstasy or near-death experiences, but they appear just as often in 5-
MeO-DMT narratives. In the moment, users often believe they have died and
passed into the afterlife, shedding their human identities as they enter the light.
The “ego,” or self, simply dissolves, leaving a boundless state of nothingness,
completely devoid of the trappings of material life. Lifelong psychedelic
researcher Dr. Stan Grof describes it beautifully:
My only reality was a mass of radiant swirling energy of immense
proportions that seemed to contain all of existence in a condensed and
entirely abstract form. I became Consciousness facing the Absolute. It had
the brightness of myriad suns, yet it was not in the same continuum as any
light I knew from everyday life. It seemed to be pure consciousness,
intelligence, and creative energy transcending all polarities. It was infinite
and finite, divine and demonic, terrifying and ecstatic, creative and
destructive—all that and much more. I had no concept, no categories for
what I was witnessing. I could not maintain a sense of separate existence in
the face of such a force. My ordinary identity was shattered and dissolved; I
became one with the Source.
Though it can be terrifying, especially when resisted, users who give in to the
experience describe it as an oceanic spiritual state—nirvana, infinity, samadhi, or
the godhead, depending on whom you ask. One thing they all agree on, though:
This state of being defies language. The 5-MeO-DMT void cannot be
communicated, analyzed, or comprehended. It can only be experienced.
AYAHUASCA
DISCOVERED DURATION
Known since antiquity 4 to 8 hours
ASSOCIATED WITH indigeneous tribes of the Amazon rainforest
FIG. 1.3
BANISTERIOPSIS CAAPI AND PSYCHOTRIA VIRIDIS
To shamans, Ayahuasca is not only a medicine but “La Madre,” a maternal entity who shares her
wisdom with human beings.
[ THE EXPERIENCE ]
In the Amazon, ayahuasca is not considered a drug, but a sacred medicine and
spiritual tool. The natives believe each plant has its own spirit, which offers a
unique blend of teachings to humanity. The decoction, then, is a sacrament in the
truest sense: Composed of benevolent plant intermediaries, it allows partakers to
commune directly with the spirit world. Indeed, among many communities,
ayahuasca visions represent a higher plane of reality; everyday consciousness is
understood to be illusory.
With the guidance of a trusted curandero, or healer, native peoples use the
vine to purge themselves of evil spirits, connect with their ancestors, and heal
various bodily and mental blockages. Aspects that Westerners would normally
consider unpleasant side effects, such as vomiting and diarrhea, are regarded by
shamans as essential characteristics of the experience, a purging of negativity in
all its forms. The goal is catharsis, not entertainment.
Ceremonies are conducted in a maloca, a communal longhouse made of
natural materials, usually round in shape with a thatched roof. For the week
before a ceremony, participants are expected to follow a strict diet that includes
no red meat, no refined sugar, no alcohol, and no spicy foods; they also abstain
from sex.
Participants sit in a circle facing one another, and each is provided a bucket
for “purging.” The curandero offers each person a cupful of the thick brown tea
and the session begins. An ayahuasca ceremony can last from 4 to 8 hours and
often consists of two or three cupfuls over the course of the evening.
For the duration of the ceremony—and often throughout the process of
mashing and boiling the ingredients beforehand—the shaman sings icaros,
spiritual songs shamans claim to have learned from the plant spirits themselves.
The shaman sings to invoke these spirits and direct the energies flowing in and
out of the maloca. If someone is having a difficult time with the medicine, the
shaman may sing a particular icaro to dispel dark spirits and protect that person
from harm. And as any psychedelic user knows, music can be used to intensify
or subdue the experience. Against a background of jungle noises that may seem
alarming and unfamiliar to nonnatives, the shaman’s icaros serve to protect,
center, and reassure.
The tea has become recognized not only as a cultural treasure, but also an economic boon to the
region.
These would-be shamans are a real problem: Though the boom in spiritual
tourism has brought money and interest to the region, it has also provided ample
opportunity for shady characters to pass themselves off as skilled shamans.
Some are simply careless and inexperienced, not yet ready to manage the intense
emotions of a group of rookie gringos who may be tasting the vine for the first
time. Others are manipulative con men and predators: There have been multiple
cases of women sexually assaulted by their so-called shamans. Perpetrated by
men posing as trusted guides in a sacred therapeutic process, these crimes
represent an especially vicious betrayal of trust.
Although ayahuasca can cause complications for those on certain medications
or with a history of mental illness, it is very rare for death to result from
consuming the drink alone. In 2012, an eighteen-year-old American died in
mysterious circumstances after consuming a high dose of ayahuasca at a healing
center. The shaman, concerned for his center’s reputation, buried the man in a
field and lied to police and the boy’s family before eventually coming clean.
Two years later, a young English man suffered a fatal reaction to the brew in
Colombia, and his body was left roadside by the locals. In 2015, a Canadian man
stabbed another man in self-defense when the latter, under the influence of
ayahuasca, became violent and attacked him.
Shocking stories like these make for sensational headlines, but they are the
exception, not the rule. Still, the risks are real. Travelers are warned to conduct
extensive research and tread with extreme caution when considering an
ayahuasca session in an unfamiliar country.
[ HEALING PROPERTIES ]
Proponents claim that a dose of ayahuasca lowers their defenses, allowing them
to unravel their traumas and deep-rooted insecurities with uncommon clarity.
Although an abundance of anecdotal evidence suggests beneficial effects on a
variety of mental conditions, very little clinical research has been conducted.
Early results are limited but promising.
A 2007 study of long-term members of the Santo Daime religion showed that
participants experienced reduced anxiety, panic, and hopelessness in the short
term. Two years later, researchers found that beginners who drank the brew
regularly over six months scored higher on surveys of emotional functioning.
Of greater interest are ayahuasca’s long-term effects. Advocates claim it helps
people overcome trauma, anxiety, depression, and addiction to drugs including
alcohol and tobacco. But where’s the science?
A landmark 1996 study led by Dr. Charles Grob, a luminary in the field of
psychedelic science, examined a small group of UDV members who had
consumed Hoasca regularly for at least ten years. He found that although most of
the experimental subjects had previously suffered from mental and behavioral
problems, including alcoholism, depression, and anxiety, none met the criteria
for any disorder at the time of the study.
Both the unusually high incidence of prior mental illnesses and their apparent
resolution are enlightening: On one hand, as something of an entheogenic self-
help community, Santo Daime tends to attract troubled and suffering people. On
the other hand, their recovery coincides with their membership in the church and
regular attendance of “works,” though it’s impossible to establish causation in a
study of such limited scope.
ASSOCIATED WITH author and speaker Terence McKenna and psychiatrist and researcher Dr. Rick
Strassman
FIG. 1.4
N,N-DIMETHYLTRYPTAMINE
[ ORIGINS AND BACKGROUND ]
HOUGH OFTEN OVERSHADOWED BY MORE POPULAR COMPOUNDS such as LSD
T and psilocybin, DMT is in many ways the quintessential psychedelic.
Unlike its better-known chemical cousins, DMT, short for N,N-
dimethyltryptamine, occurs naturally in a wide variety of plants and animals,
including the human body. Although it is by far the most common psychedelic in
nature, DMT rarely occurs in concentrations high enough to cause intoxication.
Its purpose in humans and other organisms remains a mystery, but its apparent
ubiquity in nature seems to indicate a fundamental role—if not as a
neurotransmitter, then at least as a chemical building block for other important
compounds.
For many centuries, DMT has featured as one of two chief ingredients in
ayahuasca, the plant-based sacrament revered by Amazonian tribes. More
recently, this once-obscure brew has attracted waves of “spiritual tourists” to the
jungle in search of healing, cleansing, and catharsis. DMT’s role in this
traditional context is covered in the separate ayahuasca chapter of this book (see
here). This chapter focuses on the isolated compound, which in the twentieth
century has emerged as an entheogen and exploratory tool in its own right.
Though the substance is not, gram for gram, especially potent—an effective
dose requires one hundred times more material than LSD—a full DMT
“breakthrough” is widely considered by seasoned explorers of consciousness as
one of the most powerful of all visionary experiences.
Although all of us produce and metabolize trace amounts of DMT every day,
higher doses are definitely not for the fainthearted. A peerless, sublime, and
extremely fast-paced entheogen, DMT commands respect from even the most
fearless explorers of inner space.
[ BEYOND AYAHUASCA ]
Extracted DMT comes in powder or crystal form and ranges in color from white
to yellow. It has a light but distinctive fragrance, reminiscent of sweet flowers,
but when vaporized, takes on a pungent odor somewhat like burning plastic.
DMT is occasionally injected, although this requires specialized materials and
skills. The pure compound can be consumed orally, as with ayahuasca, but must
be combined with another chemical to prevent stomach enzymes from breaking
down the DMT. Such pharmaceutical analogs of the jungle brew are known,
fittingly enough, as “pharmahuasca.”
Most often, DMT is vaporized in a glass pipe and inhaled. This has the
twofold result of compressing the timeframe of the experience while greatly
intensifying its effects. An oral formulation such as ayahuasca lasts between 3
and 5 hours; vaporized DMT is closer to 15 minutes.
A newer formulation has gained popularity in recent years. Changa, a
smoking blend of DMT-infused plant materials, originated in Australia in the
early 2000s and has since found favor among DMT enthusiasts around the
world. Like ayahuasca, changa blends usually feature both DMT and other
compounds, called MAOIs, which potentiate DMT’s effects. Changa may also
feature nonpsychoactive herbs, such as peppermint, lavender, and blue lotus. In
duration and intensity, changa lies somewhere between vaporized DMT and
traditional ayahuasca. Its many advocates appreciate the slower onset, longer
duration, and altogether more manageable experience when compared to
vaporizing pure DMT.
Word soon got out to adventurous psychedelic circles. The Beat novelist
William S. Burroughs became one of the first to try this mysterious new
chemical. It was not to his liking. In a letter to Timothy Leary, Burroughs
explained that his DMT experience was, “completely and horribly real and
involved unendurable pain.”
In the early 1960s, just as he was ramping up the Harvard Psilocybin Project,
Leary began hearing whisperings of this powerful new psychedelic. Though
Burroughs had warned him of its terrifying nature, Leary’s curiosity got the best
of him. Although it never found its way into his psychedelic research program at
Harvard, injected DMT would later become a mainstay in Millbrook, Leary’s
psychedelic haven in upstate New York.
DMT commands respect from even the most fearless explorers of inner space.
In his book High Priest, Leary described his first-ever DMT experience in the
company of a few close friends:
At that time, DMT wasn’t for the squeamish—the stigma of injecting drugs
kept all but the most dedicated explorers from trying the new psychedelic. But it
wasn’t long before Nick Sand, one of the two clandestine chemists responsible
for the iconic Orange Sunshine acid of the 1960s, made a groundbreaking
discovery: Freebase DMT could be smoked.
Vaporizing changed the nature of the experience tremendously, from a 1-hour
ride to a 10-minute rocket ship through hyperspace. This marked the beginning
of DMT’s reputation as “the businessman’s trip,” a chemical of incredible power
that blasted the user to another dimension and back in a matter of minutes.
Though it never gained widespread recognition as a 1960s countercultural
icon the way cannabis and LSD did, DMT commanded respect as a powerful
substance among those in the know—and has continued to amass a dedicated
following since its discovery.
[ THE EXPERIENCE ]
When vaporized, DMT’s effects are indescribably intense and nearly immediate.
Users speak of attempting to inhale a second or third hit while the room
dissolves into fractals around them. A euphoric, tingling “buzz” traverses the
user’s body, often coinciding with auditory hallucinations such as a rising tone or
sounds that resemble crinkling plastic. There is a strong impression of being
launched into an alien dimension. Indeed, the onset is so rapid that many users
refer to it as “blastoff.”
DMT creates a wellspring into a type of infinite space. You can feel and
taste it, as it moves through your whole being like a cool refreshing breeze
on a hot sticky day. Like a mother’s soothing touch on your fevered brow,
but much deeper and more profound. You can feel the wind of the Divine
blowing through your soul.
Many volunteers believed these entities were completely real, long after the effects of the drug
wore off.
The beings and creatures I’ve seen have been curious and various, but they
have never looked like anyone I’ve ever seen, nor any mythical creature
from history…. Although they were totally original and amazing, never did I
feel that they were strangers. I recognized them immediately. They had a
bizarre but faintly and curiously familiar feeling to them. I think that this is
significant, in that the lesson is one of personal responsibility. These are
our creatures created by the infinitely capable creative force to teach us
about ourselves. They are mirrors that help us do the difficult job of looking
at ourselves, and remembering who we are.
DOM AND THE DOX FAMILY
DISCOVERED DURATION
Alexander Shulgin in 1963 12 to 36 hours
ALSO KNOWN AS STP
FIG. 1.5
2,5-DIMETHOXY-4-METHYLAMPHETAMINE
[ THE EXPERIENCE ]
Shulgin first created DOM in 1963 while researching psychedelics for the Dow
Chemical company. He and his friends found 3 to 5 milligrams produced strong
effects. Many users report a pleasant “body high” that amplifies every tactile
sensation into a wave of pleasure, along with heightened vision and hearing.
Elaborate hallucinations are common, and users may find themselves immersed
in fully realized fantasies, especially with their eyes closed. After only 5
milligrams, one of Shulgin’s guinea pigs wrote, “I knew what it was like to look
across the brink to insanity.” At 10 milligrams, Shulgin reported, “DOM has the
glory and the doom sealed up in it.” And 12 milligrams produced tremors that
felt “like poisoning.”
Imagine the madness when DOM first hit the streets of San Francisco in the
form of 20-milligram tablets. Distributed as STP, no one at the time knew the
substance was, in fact, DOM. Said to stand for “serenity, tranquility, peace,” STP
sowed only havoc and confusion among the Haight-Ashbury hippies who took it.
Chemists quickly halved the dose, but 10 milligrams still guaranteed an intense
24-hour affair.
Thousands of such doses were distributed to attendees of the Human Be-In,
an event held in Golden Gate Park in 1967, a few months before the Summer of
Love. Because LSD had been banned in California the year before, the time was
ripe for a fresh alternative to take center stage.
But DOM’s debut was an unmitigated disaster. The high dose was
compounded by DOM’s unusually slow onset—many people, feeling no effects
after 1 hour, took another tablet, or even two. This proved to be a huge mistake.
As the Beat poet Allen Ginsberg chanted mantras, the Grateful Dead played a
heady set, and Timothy Leary urged everyone to “Turn on, tune in, drop out,”
thousands of people began to freak out.
Bay Area hospitals were soon flooded with tripping hippies. Time proved to
be the best medicine—eventually all users returned to terra firma, though
probably more than a few swore off psychedelics for life. Thankfully, nobody
died. The main casualty was DOM, whose reputation soured overnight.
[ MORE TO COME? ]
There are a whole host of DOx compounds, many of them yet untested.
Shulgin’s brilliance lay not only in mapping new molecular territories and
pushing the frontiers of consciousness forward but in providing tantalizing leads
for future explorers. Shulgin was convinced that still more variants of his DOx
creations would prove psychoactive and extended an open invitation to the
chemical trailblazers of the future.
LSD
DISCOVERED DURATION
Synthesized in 1938; psychedelic properties 8 to 12 hours
discovered in 1943 by Swiss chemist Albert
Hofmann
ASSOCIATED WITH 1960s counterculture, the Beatles, the Grateful Dead, Timothy Leary, Ken Kesey
FIG. 1.6
LYSERGIC ACID DIETHYLAMIDE
[ ORIGINS AND BACKGROUND ]
LTHOUGH IT’S THE MOST FAMOUS AND WELL RESEARCHED of all psychedelics,
A LSD is also, in the long view, one of humanity’s newest. Discovered
serendipitously by a Swiss chemist in 1938, LSD has since emerged as a
countercultural icon, therapeutic medicine, military brainwashing tool, and even
a religious sacrament. For many, it defines the term “psychedelic,” bringing to
mind the 1960s heyday where rock bands, artists, writers, and seekers of all
stripes became heavily influenced by this new and earth-shattering substance.
Some substances, upon their discovery, are developed into medicines; others
become addictive vices; and still others fade into obscurity. LSD carved its own
path, defying all expectations and weaving itself into the tapestry of history. Also
known as acid, it became so tightly bound to the zeitgeist of the 1960s that its
association with that era still echoes in the collective memory.
LSD’s fame was also its undoing. Any substance that becomes popular
among countercultural figures risks drawing the ire of the authorities. Although
it had been prescribed to tens of thousands of people in the 1950s and studied as
a therapeutic treatment for everything from alcoholism to depression, LSD was
outlawed in 1968. Yet, it soldiered on as an underground substance and is
enjoying a recent resurgence of scientific research.
LSD was, perhaps, the preeminent mind-altering substance of the twentieth
century, and, even today, is the standard by which all other psychedelics are
judged.
[ A FORTUITOUS DISCOVERY ]
LSD owes its existence to a Swiss chemist named Albert Hofmann. While
employed by Sandoz, a pharmaceutical company based in Basel, Switzerland,
Hofmann was investigating derivatives of ergot, a parasitic fungus that
contaminates rye grains and has been responsible for a number of deadly
outbreaks of food poisoning throughout history. As it often happens, this natural
poison turned out to offer some medical benefits. In 1938, Hofmann synthesized
the twenty-fifth derivative of lysergic acid—an ergot-based molecule—and
named it LSD-25. After limited testing with animals, it was deemed
unremarkable and shelved.
But five years later, motivated by what he called “a peculiar presentiment,”
Hofmann decided to resynthesize the chemical. In a fortuitous error, he
accidentally ingested a tiny amount. Though less than a full-on psychedelic trip,
the effects commanded the chemist’s attention. Hofmann began feeling restless
and dizzy. Lying down, he found himself in a “not unpleasant intoxicatedlike
state, characterized by an extremely stimulated imagination.” The chemist could
only watch as his mind’s eye was bombarded with an “uninterrupted stream of
fantastic pictures, extraordinary shapes with intense, kaleidoscopic play of
colors.”
[ BICYCLE DAY ]
Hofmann was intrigued. Three days later, he embarked on a second voyage—
this time on purpose. To be safe, he measured a conservative amount: 250
micrograms, a mere quarter of a milligram, surely too little to produce any
serious effects. He wasn’t counting on his new discovery being among the most
potent psychoactive compounds known to humankind.
In his lab notebook, he managed to write three terse lines before drifting off,
overcome by “dizziness, feelings of anxiety, visual distortions, symptoms of
paralysis, [and the] desire to laugh.” Alarmed, he asked his lab assistant to escort
him home. Due to wartime restrictions on automobile usage, they were forced to
take bicycles. It’s a strange and memorable image: Amid the carnage of World
War II, two chemists bicycle through Basel, one of them serving as LSD’s first
guinea pig, looking a bit perplexed as he maneuvers through once-familiar
streets.
He couldn’t have known it then, but this chemical experiment would mark the
beginning of a new era of human consciousness. Hofmann’s discovery
represented a psychedelic “first contact,” the very first interface between the
human mind and a novel molecule that would change history. Today, Bicycle
Day is celebrated every April 19 by LSD enthusiasts around the world,
commemorating that momentous bike ride.
LSD’s exceptional potency surpasses that of psilocybin, DMT, and mescaline by several orders of
magnitude.
The trip did not start on a pleasant note, however. Hofmann found himself
besieged by “threatening forms,” and everything he saw “wavered and was
distorted as if seen in a curved mirror.”
Safe at home, on his sofa, he did not fare any better.
The chemist became the first LSD subject to mistake the experience of “ego
death” for the more permanent kind, but he would not be the last.
As time wore on, though, his fears began to dissipate. The family doctor
arrived and assured Hofmann he was the very picture of health—the only
abnormal symptom appeared to be extremely dilated pupils.
Eventually, Hofmann discovered he was able to enjoy his unusual state of
mind. The “fantastic images,” he later wrote, were
The chemist knew right away he’d discovered something special. Between its
incredible potency, its apparent safety, and especially its ability to produce
profound shifts in consciousness, he expected LSD would have a bright future in
psychiatry. What he didn’t count on was anyone wanting to take it recreationally
—surely the experience’s intensity would dissuade any casual users.
Those who’ve had the honor of dissolving into these boundless depths often rank it as the pinnacle
of life itself.
[ THE EXPERIENCE ]
LSD takes 40 to 90 minutes to kick in; once it does, there’s no backing out. The
full experience lasts from 8 to 12 hours.
In a full-blown acid trip, there is often a sense of openness, childlike wonder,
and a heightened emotional sensitivity that can lead to indescribable bliss and
contentment or to anxiety, paranoia, and abject terror. Colors become more vivid,
borders bleed into each other, and people’s facial expressions become impossibly
poignant, hilarious, and grotesque by turns. Swirling patterns swim across every
surface, taking the form of infinite fractals, elaborate geometric structures, or
even recognizable faces. Cognitive shifts lead to nonlinear thought patterns,
compassionate yet honest self-analysis, a renegotiation of old assumptions and
habits, expansive curiosity, and, in some cases, fears about going insane or
dying.
Trips vary tremendously based on many circumstances. Seemingly minor
thoughts or environmental cues can send a naïve user flying into a sublime state
of oneness or spiraling into a hellish spiritual crisis. As Albert Hofmann’s
maiden voyage demonstrates, the two extremes may even occur in the same trip.
One of the hallmarks of a deep acid experience is the dissolution of what is
commonly known as the ego—the self, the “I,” the conscious being with its own
experiences and memories, distinct from the rest of the universe. This “ego
death” can be terrifying. But if the user surrenders to it, it can also be beautiful—
a sense of oneness, of absolutely boundless and infinite love, a state
indistinguishable from spontaneous religious experiences described by monks,
prophets, and ascetics since time immemorial. For committed psychonauts, ego
death is the holy grail of tripping. Those who’ve had the honor of dissolving into
these boundless depths often rank it as the pinnacle of life itself.
INTRODUCING
THE MICRODOSE
Psychedelics are famous for producing intense emotional journeys, but the relatively new
phenomenon of “microdosing” turns that on its head. A microdose is one-twentieth to one- tenth of a
normal dose of LSD, or another psychedelic, taken once every few days with the aim of improving
mood, creativity, and general well-being. The dose is far too small to send one on a trippy voyage, but
just enough to bring a certain “lift” to one’s daily activities. Showing up to work on acid might sound
like a terrible idea, but advocates of microdosing claim it actually improves focus and performance.
Supposedly, even Albert Hofmann indulged in the occasional LSD microdose and argued the
“subperceptual” dose was an understudied aspect of psychedelics.
The microdosing trend has exploded in popularity in recent years, especially in the psychedelic
hotbed of San Francisco. Silicon Valley techies, writers, artists, and thousands of other people around
the world have shared anecdotes about the benefits of microdosing in recent years, but science is just
catching up. A new study enrolling more than 1,500 respondents found a number of tentative but
promising results. Migraine sufferers report their headaches are greatly reduced in intensity and
duration. Students report improved grades and better focus, and some women who had experienced
painful or emotionally troubling periods report healthy, pain-free cycles. Others indicate
improvements in their relationships, a greater sense of openness and gratitude, and reductions in
depression. The self-reported benefits have not yet been tested in a strict scientific setting to eliminate
placebo effects, but they suggest avenues of future research. And best of all, because doses are so low,
adverse effects are practically unheard of.
Starting in the early 1970s, LSD research stopped cold for more than forty
years. In 2014, MAPS (Multidisciplinary Association for Psychedelic Studies)
published a study triumphantly breaking the silence. It showed that when
combined with talk therapy, LSD reduced anxiety in patients with terminal
illnesses. Death-related anxiety is exceptionally difficult to treat. Because its
origins are existential rather than chemical, traditional medications offer little
solace. LSD-assisted psychotherapy provided relief for the majority of subjects;
as patients grappled with their own mortality, they emerged with a new
perspective on death, intent on maximizing the value of their remaining days. It
was a lasting peace; twelve months later, surviving patients still showed reduced
anxiety and improved quality of life.
In 2016, researchers at London’s Imperial College produced the first-ever
brain scans of people tripping on LSD. The images—analyzing both blood flow
and electrical activity in different regions of the brain—showed an expanded
state of visualization, even while subjects remained in a dark MRI machine with
their eyes closed. According to the study’s authors, Dr. David Nutt and Dr.
Robin Carhart-Harris, the visual cortex became much more connected to
disparate parts of the brain than in sober consciousness.
Another effect, which rose and fell in concert with subjects’ reports of “ego
dissolution” and feelings of oneness with their environment, was the dampening
of what’s known as the default mode network (DMN)—a widely distributed
group of neurons that fire together while the brain is at rest, not focusing on any
particular task. According to Nutt and Carhart-Harris, their results show this
network is at least partly responsible for the sense of self we call the “ego.” LSD
appears to produce its famous boundary-blurring effects by reducing
coordination between neurons in the DMN. So LSD’s “mind-expanding” effects
are due to overall greater “crosstalk” between brain regions that usually remain
isolated. By quieting the role of the ego, LSD produces a more connected—
albeit more chaotic—brain.
Early research often focused on LSD’s potential in treating alcoholism. A
2012 meta-analysis of six of the best studies from that era, consisting of more
than five hundred total subjects, found that acid does in fact reduce problematic
drinking, at least short term. A single dose significantly reduced alcohol abuse
for several months afterward.
Another condition that’s notoriously difficult to treat is cluster headaches,
which cause excruciating pain. A 2006 study found that, for 80 percent of a
small group of people suffering from cluster headaches, LSD eliminated their
headaches and extended the period between them. Five years later, a second
study showed that 2-Bromo-LSD—a derivative first developed by Albert
Hofmann—may be just as effective, without producing any of the psychedelic
symptoms of its more famous namesake.
A flurry of other studies have produced interesting results. A 2015 study
found no link between mental health problems and the use of LSD and
psilocybin in 19,000 randomly selected psychedelic users. Another study in the
same year found that people on LSD produced feelings of “happiness, trust,
closeness to others, [and]… emotional empathy,” while impairing the ability to
recognize sad and fearful faces. Yet another 2015 study—coauthored by Dr.
Carhart-Harris, who produced the first LSD brain scans—demonstrated the
compound’s ability to increase creative imagination and suggestibility. That
won’t surprise anyone who’s tried acid, but it may prove medically relevant as
suggestibility has proved helpful in treating conditions like chronic pain and
depression.
Two recent studies demonstrated a heightened emotional response to music.
In the first, people’s reactions to music featured especially high ratings of
“wonder,” “transcendence,” “power,” and “tenderness.” In the second study,
conducted in Switzerland in 2017, researchers teased apart a fundamental aspect
of human consciousness: the attribution of meaning. When sober, people listened
to selections of “free jazz” music and found it unengaging. On LSD, they not
only found the music pleasant and personally meaningful, but described
instances of synesthesia, such as hearing colors and seeing sounds. The
substance not only enhances our emotional sensitivity, but allows us to perceive
deep personal meaning where none existed before.
Albert Hofmann was heartened by the resurgence of research. Before he died
in 2008, at the ripe age of 102, he witnessed the beginning of LSD’s
rehabilitation in science and public opinion. He had watched his creation, which
he dubbed his “problem child,” come full circle—from an unexpected but
promising birth, through a worrying adolescence of excess and abandon, and
finally to the first signs of an adulthood rooted in moderation and rationality.
MORNING GLORY
DISCOVERED DURATION
Known since antiquity 4 to 10 hours
ASSOCIATED WITH the Aztecs, Maya, and native tribes of Mexico
KEY COMPOUNDS ergine (LSA), isoergine, methergine
FIG. 1.7
TURBINA CORYMBOSA (SHOWN), IPOMOEA TRICOLOR, ARGYREIA NERVOSA, AND OTHERS
[ A BOTANICAL DISPUTE ]
Though scholars had identified ololiuhqui as a morning glory species as early as
1854, the hallucinogen’s true identity was disputed for many years. It was
Richard Evans Schultes who finally settled the matter. Having observed its use
by Zapotec medicine men, Schultes collected samples of Turbina corymbosa and
sent them to Albert Hofmann, the chemist who had discovered LSD.
Morning glories have earned a newfound popularity among those looking for psychedelic
euphoria without the legal woes.
[ THE EXPERIENCE ]
The high from morning glory seeds has been compared to LSD, but is often
regarded as more placid. The cocktail of lysergic chemicals in the seeds is less
stimulating than their more famous cousin and has even been called sedating.
Nausea is extremely common, but often passes after vomiting.
Dr. Humphry Osmond, a British-born psychiatrist who introduced Aldous
Huxley to mescaline, became curious about these hotly debated seeds. In 1955,
he engaged in a series of self-experiments. On the first few occasion, the seeds
had little effect. But his later experiences—with sixty and then one hundred
seeds, pulverized with a mortar and pestle—were more powerful.
Osmond’s terse notes provide a window into the first recorded encounter of a
Westerner with the famed Mexican sacrament.
People irritate; things fascinate; the texture of wood; the almost metallic
gold center of an African violet. Mildly nauseated. The little warm dog on
my lap the only contact.
…still a depth and brightness in things such as they have on a May morning
when you are twenty-one. A newness, freshness as if everything had had a
shower.
Osmond’s experience may not be typical. Many takers of morning glory and
Hawaiian Baby Woodrose seeds have reported all the usual hallmarks of
psychedelic experiences: swirling, kaleidoscopic imagery, bizarre physical
sensations, emotional sensitivity, and even the breakdown of time and space.
Osmond may be the first non-Native American to consume the seeds and report
the results, but his experience of “irritable apathy” was hardly definitive.
FIG. 1.8
LOPHOPHORA WILLIAMSII
[ ORIGINS AND BACKGROUND ]
NE OF HUMANITY’S OLDEST PSYCHEDELIC TRADITIONS, the peyote ritual was
O already several thousand years old when the Spaniards encountered it in
the sixteenth century. The cactus, long revered by natives as a sacred
visionary medicine and a central pillar of their way of life—even recognized by
some tribes as a deity itself—was viciously suppressed by the invading Spanish
forces who had very different views on God and holiness. What the natives saw
as the gateway to spirituality, the Conquistadors condemned as a satanic drug
scourge.
Since then, peyote has remained a point of tension between native and
European peoples in the Americas. Today, despite its prohibited status in the
United States, peyote use is permitted for members of the Native American
Church. It is one of only two religious sacraments exempt from federal drug
laws; the other is ayahuasca (see here).
Peyote is native to the deserts of Mexico and southern Texas, where it grows
extremely slowly: It can take more than ten years for a plant to reach maturity.
Unable to regrow fast enough to keep up with demand, peyote has been
overharvested. Luckily, it grows well in greenhouse conditions.
The plant looks innocuous enough—a small, fuzzy green cactus without any
spines. The majority of the plant extends underground like a carrot. What remain
aboveground are the crowns, which can be cut and cured into “buttons” or
mescals for ritual consumption, leaving the plant intact to grow new crowns.
Upon each crown, wavy furrows extend outward from the center like twisted
spokes, lending a geometric, almost symbolic, look to the humble green bulb. At
the center grows a single flower with brilliant pink petals.
[ THE EXPERIENCE ]
Peyote’s quaint appearance belies its profound effects on the human mind, which
have been utilized for healing and journeying by native peoples for countless
generations. It can be consumed raw, dried, or as a bitter tea. The name derives
from the Nahuatl peyotl, meaning “divine messenger.”
Nausea and vomiting are very common in the early stages, and some say
peyote gives you the hangover before the experience. This quickly gives way to
full-fledged psychedelia, including vivid kaleidoscopic imagery, enhanced
empathy, and often-profound spiritual experiences. The effects are reminiscent
of psilocybin mushrooms or LSD, but many find peyote milder and less
disorienting, perhaps due to the difficulty of choking down more than a handful
of the extremely bitter buttons. Overall, a peyote trip takes between 8 and 12
hours. The cactus contains hundreds of alkaloids, but its primary psychedelic
constituent is mescaline.
It is called Peiotl. It is white…. Those who eat or drink it see visions either
frightful or laughable. This intoxication lasts two or three days and then
ceases. It is a common food of the Chichimeca, for it sustains them and
gives them courage to fight and not feel fear nor hunger nor thirst. And they
say that it protects them from all danger.
The natives used peyote for a variety of purposes, such as finding lost or
stolen items, foretelling the future, and healing almost any malady—from fever
and sunstroke to headaches and arthritis. Some tribes used it as a salve for burns
and wounds and even to improve endurance in footraces and long hunts.
In 1690, Padre José de Ortega gave the first known description of the peyote
ritual itself, which to this day involves hours of dancing, singing, and crying as
the cactus’s ecstatic trance takes hold:
Peyote’s quaint appearance belies its profound effects on the human mind.
Close to the musician was seated the leader of the singing, whose business
it was to mark time…. Nearby was placed a tray filled with Peyote, which is
a diabolical root that is ground up and drunk by them so that they may not
become weakened by the exhausting effects of so long a function… One
after the other, they went dancing in a ring or marking time with their feet,
keeping in the middle the musician… They would dance all night, from five
o’clock in the evening to seven o’clock in the morning, without stopping nor
leaving the circle.
The Spaniards’ rigid Catholicism left no room for such “heathen rituals and
superstitions” and consuming peyote was declared an egregious sin. To the
natives, who had honored peyote as a sacred plant and portal to the divine, it was
as though the white invaders had outlawed God Himself.
A tradition of such power and longevity would not die easily and peyote
rituals continued in secret. Even as it shrank from public life, peyote continued
to expand northward to new territories, winning over indigenous peoples who
lived beyond the cactus’s natural habitat and had to acquire the contraband by
commerce.
Today, the peyote cult extends far beyond the Chihuahuan Desert and is used
ceremonially by Apache, Comanche, Navajo, and other tribes stretching across
the Great Plains as far north as Canada. Customs vary, but a few factors are
common: Gatherings are usually held at night around a blazing bonfire, with
much singing and dancing. At the center of the ceremony, of course, is peyote—
and the gods and ancestors to whom it offers a direct and powerful communion.
[ THE HUICHOL ]
Anthropologists believe the traditions of today’s Huichol people bear the closest
resemblance to the peyote rites of centuries past. Every year, the Huichol
mara’akame, or shaman, leads a pilgrimage to the holy land of Wirikuta, three
hundred miles (483 km) from their home. He is joined by a group of pilgrims
that includes men, women, and children.
Today, any member of the Church may partake in its peyote ceremonies, regardless of ethnicity.
At the sacred grounds, the pilgrims perform a ritualized ceremony and gather
peyote to bring back to their people—enough to use for an entire year and to
trade to nearby tribes who have no such harvest.
The Huichol are also famous for their vision-inspired art, which bursts with
spectacular colors and geometric designs. The yarn paintings and beaded objects
are now popular as tourist items but are still rooted in the tribe’s longstanding
aesthetic language. Motifs such as deer, corn, and peyote are rendered in
stunning color, interwoven with hypnotic patterns representing the visions
induced by the cactus. These psychedelic artworks are also created as offerings
and left at mountain shrines and other holy locations to express gratitude to the
gods.
Blake wasn’t talking about mescaline, but he may as well have been. The
same sentiments have been echoed by the Huichol and other indigenous tribes,
who believe this world is illusory. To them, true reality is revealed in the visions
granted by the sacred peyote, the great cleanser of the doors of perception.
Osmond replied with his own proposal, formed from the Greek roots psyche (mind) and deloun
(show or manifest):
The name stuck. Sorry, Aldous, but it’s for the best—the “Phanerothymic Sixties” just doesn’t have
the same ring to it.
PSILOCYBIN MUSHROOMS
DISCOVERED DURATION
Used by natives in the Americas for at least five 3 to 6 hours
centuries
ASSOCIATED WITH Terence McKenna, Timothy Leary
KEY COMPOUNDS psilocybin and psilocin
FIG. 1.9
PSILOCYBE CUBENSIS (SHOWN) AND ALMOST TWO HUNDRED OTHER SPECIES
[ ORIGINS AND BACKGROUND ]
NOWN AS TEONANÁCATL TO THE AZTECS, ’nti-si-tho to the Mazatec, magic
K mushrooms to the hippies, and simply “shrooms” to the modern enthusiast,
psilocybin-containing fungi have many names—and many fans. Today, the
humble mushroom is one of the best-known members of the psychedelic family,
represented by hundreds of species growing all across the world. So it’s hard to
believe they were once a well-guarded secret known only to a handful of native
peoples in Central America. Their very existence was doubted by top
anthropologists and biologists until recently, thanks to a centuries-long campaign
by Spanish invaders to stamp out the “demonic” mushrooms.
The Catholic authorities were ultimately unsuccessful. Today, no one doubts
the existence of these little toadstools, nor their incredible power. The
mushrooms have returned in full force, and their active components, psilocybin
and psilocin, are shaking up the worlds of neuroscience and medicine.
The quaint mushrooms and the mystical realms they unlock have a universal
and timeless appeal. From the mountains of Mexico to the halls of Harvard, from
the centuries before Christ to the age of the Internet, for shamans and healers,
professors, reverends and inmates, psilocybin has shifted perspectives and
granted vistas of vast new worlds within.
[ THE EXPERIENCE ]
The effects of psilocybin mushrooms last between 3 and 6 hours and produce a
wide range of sensory and emotional distortions ranging from animated visual
patterns to deep personal insights. For many, mushrooms represent the definitive
psychedelic experience.
Changes to the senses become apparent within 30 minutes of ingestion.
Textures and patterns drift through the air, melting into arabesques and
undulating geometries. Colors become impossibly rich, memories come alive
with the vitality of the present moment, words and faces are imbued with an
unfathomable poignancy, and the ears open up as if for the first time, revealing
previously ignored details in the sonic landscape.
Often, traumas and insecurities bubble to the surface of one’s consciousness.
If the user is prepared to confront and sit with them, profound healing is
possible; if not, the trip may take a dark and unpleasant turn. A handbook used in
psychedelic therapy sessions encourages subjects to embrace difficult feelings,
even if the first instinct is to recoil: “Look for the darkest corner in the basement,
and shine your light there.”
With the right dosage and setting, psilocybin is well known for providing
mystical experiences characterized by the dissolution of one’s sense of self,
leaving only a boundless impression of cosmic unity and bliss. Reports of
encounters with God, spirits, or benevolent forces are common. Those lucky
enough to experience such a state often rank it as one of the most meaningful
moments of their lives.
Where the Aztecs saw God, the Spaniards perceived only the nefarious work of the devil.
MARÍA SABINA’S
“LITTLE CHILDREN”
R. Gordon Wasson’s story in Life profoundly influenced the psychedelic movement of the 1960s and
led many people to visit María Sabina, the Mazatec healer who had shared the secret of the mushroom
with him. After reading the article, Timothy Leary traveled to Mexico and had his own mushroom
experience, which ignited his journey as psychedelic researcher and countercultural icon. If it weren’t
for Wasson’s expedition, “shrooms” may have remained an obscure mystery, and Timothy Leary may
never have become a household name.
In the next decade, thousands of other spiritual tourists, including Bob Dylan, John Lennon, and
Mick Jagger, all descended upon Sabina’s village in the hopes of tasting the divine mushroom. Even
the chemist Albert Hofmann visited, offering the healer a bottle of pure psilocybin pills. María Sabina
sampled them and agreed the experience was much the same as that afforded by her “little children.”
It wasn’t all good news for the traditional Mazatec community, however—the village became
thronged with gringos, and María Sabina eventually came to regret serving the mushrooms to
foreigners.
[ PSILOCYBIN RESEARCH ]
Psilocybin research trailed far behind that of LSD in the 1950s and ’60s, but it
did garner its share of groundbreaking studies. After the mushrooms’ prohibition
in 1970, research halted for decades, but psilocybin is now emerging as the
cornerstone of contemporary psychedelic research. Today, it’s being examined
for its role in treating anxiety and alcoholism, helping people quit smoking, and
other uses.
One of the first tasks was to isolate the active components that made the
mushrooms “magic.” Samples were sent to Albert Hofmann, the Swiss chemist
who had discovered LSD in 1943. Hofmann identified two serotonin-like
compounds responsible for the mushrooms’ remarkable mental effects and
named them after the genus Psilocybe: psilocybin and psilocin.
Today, it’s being examined for its role in treating anxiety and alcoholism, helping people quit
smoking, and other uses.
[ MODERN RESEARCH ]
For many years, psychedelic research evaporated entirely. In 2006, a study led
by Roland Griffiths at Johns Hopkins University began to reverse that trend. Dr.
Griffiths chose to revisit the same question that had motivated the Good Friday
Experiment many years earlier: Can psilocybin produce religious experiences?
Griffiths found that not only did psilocybin induce “mystical-type” experiences
but such experiences carried profound meaning that continued far beyond the
original study’s duration. More than a year later, subjects ranked their experience
on psilocybin as one of the most “personally meaningful and spiritually
significant” events of their lives. In another study conducted by Griffiths in
2011, volunteers reported a range of beneficial effects after psilocybin sessions,
including lasting improvements to their attitude, mood, and behavior.
Another study found that psilocybin-induced mystical experiences resulted in
long-term changes to one of the fundamental aspects of personality, “openness.”
When this basic personality trait—encompassing one’s curiosity, preference for
variety, tendency to fantasy, aesthetic sensitivity, and attentiveness to internal
feelings—was measured, subjects scored higher for more than a year after a
psilocybin-induced mystical experience. This marked the first time in the history
of psychology that a single event had caused lasting changes in one of the
foundational domains of human personality.
For neuroscientists, psilocybin has proved to be a useful tool that not only
produces novel effects but helps shed light on how our brains normally function.
In a study led by Robin Carhart-Harris at London’s Imperial College, brain scans
taken during a psilocybin experience revealed patterns of activity that resembled
the dreaming mind. The results demonstrated for the first time the physical
underpinnings of the surreal and often dreamlike fantasias revealed by
psilocybin.
It has long been assumed that “mind-expanding” substances act by increasing
brain activity. But in a groundbreaking 2012 study, brain scans of volunteers
tripping on psilocybin revealed the exact opposite. In fact, the compound
reduced activity in several of the brain’s key connective hubs.
This led to greater communication between normally unrelated regions of the
brain. These changes were closely associated with the subjective experience of
“ego dissolution,” where one’s sense of self melts into a boundless oceanic state.
Psilocybin appears to produce at least some of its effects by inhibiting the parts
of the brain responsible for maintaining the ego, unlocking what Dr. Carhart-
Harris calls, “a state of unconstrained cognition.”
FIG. 1.10
ECHINOPSIS PACHANOI
[ ORIGINS AND BACKGROUND ]
HOUGH IT GROWS IN THE SUN, SAN PEDRO has been thriving in the shade of
T relative obscurity for many decades. In popular culture, the cactus is
overshadowed by Peru’s much better known entheogen, ayahuasca (see
here), whose popularity has erupted in recent decades. Today, ayahuasca is a
cottage industry that draws thousands of spiritual tourists to the jungle every
year, but very few make the trek for the equally powerful San Pedro ceremonies.
And as a mescaline-containing plant, San Pedro is outshined by its cousin the
peyote cactus, whose ceremonial use has expanded from the Chihuahuan Desert
of Mexico to various Native American tribes across the United States. Though
they produce the same psychedelic compound, peyote and San Pedro cacti thrive
in very different habitats on separate continents and have unique traditions of use
among the indigenous tribes that revere them.
San Pedro’s relative obscurity is no fault of the plant itself, which is prevalent
throughout the Andes Mountains of South America. Unlike peyote, which takes
decades to mature into a short, inconspicuous button, the San Pedro is a tall, fast-
growing giant. Its stalks can easily grow to 10 or 20 feet (3 to 6 m) in height, and
a plant often grows 12 inches (30.5 cm) or more in a year.
[ THE EXPERIENCE ]
Like its cousin peyote, San Pedro is a dyed-in-the-wool psychedelic plant. The
8- to 12-hour trip usually includes all the mind-blowing hallmarks of
psychedelia: kaleidoscopic visions, profound epiphanies, intense or even
contradictory feelings, and distortions of time and space, for starters. Though the
visual hallucinations can be astounding in their own right, they often take a
backseat to the spiritual and emotional qualities of the experience. A bit of
nausea is common, but usually subsides.
As with the other visionary plants they encountered, the Catholic Spaniards
who colonized Peru condemned San Pedro. “This is the plant,” wrote one
missionary,
with which the devil deceived the Indians… in their paganism, using it for
their lies and superstitions… those who drink lose consciousness and
remain as if dead…. Transported by the drink, the Indians dreamed a
thousand absurdities and believed them as if they were true…
FIG. 1.11
ANADENANTHERA PEREGRINA (SHOWN) AND ANADENANTHERA COLUBRINA
[ ORIGINS AND BACKGROUND ]
Though little known among psychedelic enthusiasts of modern Western cultures,
the seeds of Anadenanthera trees—variously known as yopo, cohoba, cebil, or
vilca—have long garnered great respect among indigenous cultures in South
America. In parts of Colombia, Peru, Brazil, Venezuela, and Argentina, shamans
use these seeds as everything from healing medicines and divination tools to
casual stimulants and even hunting aids. At one time, the use of Anadenanthera
snuffs also spread across much of the Caribbean.
When Spanish invaders first observed yopo ceremonies in the fifteenth
century, they were horrified. As zealous Catholics with no visionary sacraments
of their own, they could only conclude the natives were possessed by demons.
After taking yopo and tobacco, wrote one missionary in 1560, the natives,
“become drowsy while the devil, in their dreams, shows them all the vanities and
corruptions he wishes them to say and which they take to be true revelations.”
The natives didn’t see it that way. To many tribes, especially in the Orinoco
River basin of Colombia and Venezuela, these seeds served—and continue to
serve—vital spiritual and medicinal functions. Shamans would inhale the
powder to learn the nature of a patient’s disease and combat it, or to protect his
tribe from witchcraft and illness, or to foretell the future. Among some tribes,
yopo also served a more casual function, being used by adult males as a
stimulant or consciousness enhancer.
Anadenanthera species are tall, hardy trees, growing to 60 feet (18 m) in
height, with narrow branches and small round leaves that resemble those of
locusts. They are immediately identifiable by the footlong (30.5 cm) seedpods
dangling from their branches, which bear between six and sixteen seeds of a
brilliant blood red hue. To unlock the tree’s powers, the natives remove the
seeds, roast them over a fire, grind them to a fine powder, and forcefully inhale
them through their nostrils.
[ THE EXPERIENCE ]
Native traditions allow for many ways to consume yopo and vilca. The seeds
may be eaten, which is said to cause intense vomiting, or simply chewed and
held in the mouth until the active compounds are absorbed through the mucous
membranes. A few tribes smoke the seeds, which produces a shorter, more
intense experience. Among some cultures, the leaves and seeds are even crushed
into a liquid and used for enemas. According to at least one modern scholar, the
plants are indeed psychoactive when absorbed rectally—oh, the glamour of
studying indigenous intoxicants.
Most often, however, the seeds are roasted, pulverized into a snuff, and
inhaled into the nostrils, usually with the aid of honored artifacts, including
polished wooden snuff trays and strawlike tubes made of heron bones. Often, but
not always, the powder is mixed with lime from snail shells or the ashes of other
plants before snuffing.
Inhaling the snuff produces an intense burning sensation and a fit of sneezing.
As the active compound begins to take hold, the shaman will shiver, convulse,
and enter a state of frenzied delirium. It’s no wonder early Spaniards saw the
work of the devil as they observed the fire-lit faces of natives contorting into
grotesque positions, shrieking with wild eyes and running noses, after sniffing
the “malignant powder.”
COHOBA, THE CARIBBEAN SNUFF
There is evidence that yopo snuffs were once cultivated and consumed throughout the Caribbean.
Snuffing artifacts from preconquest times have been discovered throughout the Greater Antilles.
Christopher Columbus, on his second voyage to the New World, remarked upon the Taíno natives on
the island of Hispaniola, who would sniff a powder and “lose consciousness and become like drunken
men.”
A friar hired by Columbus to study the Taíno culture wrote that this intoxicating snuff was called
cohoba. “They take it with a cane about a foot long [30.5 cm],” wrote the friar, “and put one end in the
nose and the other in the powder” to inhale the snuff. Yet, the botanical source of this snuff remained
an enduring mystery. More than four hundred years later, cohoba was finally identified as
Anadenanthera peregrina—the same plant as yopo.
After this initial phase, the shaman begins speaking in tongues and
gesticulating wildly, a language of the whole body understood only by the
spirits. If he is treating a sick patient, the shaman learns from the spirits the
nature of the illness and draws on their powers to cure it.
As is typical of psychedelics, the inner experience is more illuminating than
the physical effects apparent to bystanders. The visions last for 20 minutes, and,
according to some sources, usually appear in black and white. The
hallucinations, in contrast to many other psychedelics, tend toward flowing
arabesque shapes rather than linear, geometric patterns. It is rare for the visions
to take any realistic or figurative forms, instead remaining abstract. At high
doses and in low light, these swirling motifs may surround the user in three
dimensions, eminently real yet untouchable.
Perhaps unsurprisingly, this painful habit of sniffing these powders has not
caught on outside of its native context. Nor has bufotenine, the chief
psychoactive component, emerged as a desirable compound on the modern
recreational market, the way other native intoxicants have, such as cocaine,
mescaline, and DMT. In fact, hardly anyone cops to having consumed pure
bufotenine, and those who have rarely recommend the experience.
Jonathan Ott, like most psychonauts dedicated enough to try this compound, did not enjoy the
experience.
EMPATHOGENIC PSYCHEDELICS
Though less overtly “trippy” than other substances, the empathogens
—literally “creating empathy”—still amplify emotions and insights in
a decidedly psychedelic way. The crown jewel of the empathogens is
MDMA—better known as Ecstasy—which today leads the revival of
psychedelic medicine.
MDA
DISCOVERED DURATION
German chemists Carl Mannich and Willy 4 to 6 hours
Jacobsohn in 1910
ASSOCIATED WITH psychedelic 1960s and experimental psychotherapy
FIG. 2.1
3,4-METHYLENEDIOXYAMPHETAMINE
transposed out of the body and to a place above and to the right rearward. I
was compelled to turn my head several times and look into that upper
corner of the room in wonder at what part of me could be up there…
Then, he began hearing footsteps. Peeking his head out of the room, he found
no one in the corridor. Yet the footsteps persisted. Finally, he looked out his
sixth-floor window. Sure enough, every time he heard footsteps, he saw a
pedestrian walking down the sidewalk far below. The researcher was astounded
—the distant shuffling of feet, too soft to have ever warranted his attention
before, now resonated with crystal clarity and commanded his full concentration.
[ THE EXPERIENCE ]
MDA defies easy categorization. Because of its tendency to produce emotional
warmth and openness, it is often classed as an empathogen (generating empathy)
alongside MDMA. But compared to MDMA, MDA is more stimulating,
providing a “rush” like that of cocaine or amphetamine. It sometimes exhibits
trippy qualities, such as synesthesia (blending of the senses), slowing of time,
and an ineffable sense of oneness with the universe, but these pale in comparison
to stronger psychedelics. Milder than LSD yet more mind-bending than
amphetamine, MDA occupies an agreeable middle ground somewhere between
stimulants, psychedelics, and empathogens.
For most people, MDA is not an especially visual molecule; the most
prominent effects are emotional. A small 1974 study summarized the effects
nicely: Most of the subjects felt, “more relaxed, happier and more at peace with
the world during the experience,” as well as “more calm, more free, more loving
and felt more like paying close attention to their surroundings.” Even more
striking, more than half the subjects reported
that as a result of the experience, the meaning of life was clearer, that life
has new significance and that they were able to discern new connections
between certain events or experiences that they had not been aware of
before.
With its ability to break through people’s internal barriers, the researchers
speculated MDA may offer help to those struggling with “obsessive, anxious, or
depressive patterns” of thinking. They found the substance facilitated “increased
introspectiveness, heightened self-awareness, and greater intuitiveness [as well
as] relaxation, acceptance, calmness and serenity”—the perfect mix of qualities
for psychotherapy.
MDA occupies an agreeable middle ground somewhere between stimulants, psychedelics, and
empathogens.
[ SIDE EFFECTS ]
Though a relatively safe substance when taken under medical supervision, MDA
has its share of dangers. As a strong stimulant, it can be dangerous for people
with heart conditions or high blood pressure. But an overdose can be life
threatening for anyone, and a few fatalities have been reported (see sidebar
MDA and Secret Experiments).
Given MDA’s prevalence of use, the overall incidence of medical
emergencies is quite low. For most users, the main concerns are psychological,
as the substance can surface unwanted memories or feelings and lead to
overwhelming sensations.
Not only was such a subject able to describe what others felt, e.g., “A is
thinking of sex with B,” or, “I think C is lost in childhood memories or
relationship fantasies with D,” but they were also able to say something
about the cues that led to these conclusions—the way someone’s body was
now dripping with sand, the way the lines formed around a person’s mouth,
or the way somebody looked over there and then looked away.
Most of the time, these assertions turned out to be correct. “It was
remarkable,” Zinberg wrote, “and it gave me some sense of why some
psychedelic users of my acquaintance had become so interested in ESP.”
MDA clarifies your life, puts everything in a correct perspective for you…
You come out with a good feeling about yourself. It helps you to see all your
difficulties in a different light, and they cease to be difficulties…. It brings
you into the experience of the moment.
For Naranjo, MDA’s chief value lay in its powerful ability to retrieve old
memories. Regression to childhood “occurs so frequently and spontaneously that
this can be considered a typical effect of this substance, and a prime source of its
therapeutic value.” According to Naranjo, episodes of “age regression” play a
critical role in a person’s journey of healing.
Such trials require significant funds and the navigation of complex
bureaucratic hurdles, however, so while MDMA marches ever closer to
prescription status, legalized MDA-assisted therapy remains a distant dream. It’s
a cruel irony that the original love drug—so magnetic and memorable in its
effects—should be left behind and forgotten, buried in the sands of history
without so much as a good-bye.
MDMA
DISCOVERED DURATION
German chemist Anton Köllisch at Merck in 1912 3 to 5 hours
ALSO KNOWN AS Ecstasy, Molly, X
ASSOCIATED WITH raves and electronic dance music; psychotherapy for PTSD
FIG. 2.2
3,4-METHYLENEDIOXYMETHAMPHETAMINE
[ THE EXPERIENCE ]
It’s easy to see why MDMA appeals to such a diverse cross section of society. If
alcohol is a social lubricant, MDMA is a full tune-up of body and mind,
generating a sense of physical, emotional, and spiritual well-being. It
temporarily smoothes over the cracks of doubt and despair that mar even the
hardiest of human souls. For a few hours, it paints a picture of true mental
health, insecurities crowded out by bubbles of confidence and an all-
encompassing sense of serenity. Far from an escape, it feels more like a coming
to terms—with oneself, with reality, with the blessed beauty of existence.
Enthusiasts say it can provide all the personal insights of psilocybin or LSD,
without the mind-bending and, sometimes, dark surprises these psychedelics are
known for.
As an agent of openness, MDMA allows uninhibited communication of
difficult or repressed subjects among friends, lovers, and therapists and their
clients. As a stimulant, it intensifies one’s focus and attention to razorlike
sharpness, while unleashing reservoirs of latent energy. And in an age of
distraction, MDMA demands engagement—with the immediate environment,
with the needs and desires of people nearby, with one’s own body, and with fears
and insecurities long suppressed. In its uncanny ability to engender a sense of
serenity and self- acceptance, MDMA is unmatched.
Physical effects are similar to other amphetamine-based stimulants:
seemingly endless energy, muscle tension, teeth grinding, and pupils wide as
saucers. MDMA also enhances the pleasure from exercise and tactile sensations
—dance, touch, and massage transcend the realm of merely “pleasant” activities
and become sublime, even for those normally too shy to partake. Sex is another
story—though erotic touch is amplified, many men find it very difficult to
achieve an erection. The paradox of the “love drug” is that it unites minds and
bodies together, but stymies efforts at sexual communion.
If alcohol is a social lubricant, MDMA is a full tune-up of body and mind, generating a sense of
physical, emotional, and spiritual well-being.
MDMA is like that impulsive, charismatic friend whose charms you can’t resist.
Today raves are bigger than ever. Having emerged from underground, the
raving subculture has spawned massive festivals like Tomorrowland and Electric
Daisy Carnival, which draw hundreds of thousands of attendees every year. The
twenty-first century’s answer to Woodstock, these festivals bring the principles
and aesthetics of 1990s raves to the big stage.
With a focus on positive connections, togetherness, and love—not to mention
hours of intense physical exertion—it comes as no surprise that ravers would
favor MDMA over other substances.
[ THE CRACKDOWN ]
National media outlets started reporting on the MDMA sensation in 1985, often
with cautious optimism as an experimental therapeutic tool. But in June of that
year, the federal government banned MDMA. It was placed in the most
restrictive category, Schedule I, reserved for substances with a high potential for
abuse and no accepted medical use.
An outcry from psychiatrists and psychologists, who had planned to utilize
MDMA’s unique effects in ongoing research and therapy, culminated in a series
of hearings about the substance’s ultimate fate. In spite of the evidence presented
at the hearings, the head of the U. S. Drug Enforcement Administration
permanently confirmed MDMA’s Schedule I status in 1986. This not only made
criminals of all personal users but also effectively halted all research and forced
MDMA psychotherapy underground.
[ THE PHARMACOLOGY OF MDMA ]
MDMA is like that impulsive, charismatic friend whose charms you can’t resist.
But instead of convincing you to blow your savings on a wild weekend in Vegas,
it induces the brain to release its natural stores of serotonin, dumping out happy
chemicals like candy from a piñata. MDMA also acts as a potent releaser of
dopamine—the chemical basis of the brain’s reward network—as well as
norepinephrine, a hormone that normally primes the body for action during times
of emotional stress and physical activity.
MDMA also causes a spike in oxytocin, a hormone associated with social
bonding, as well as cortisol, whose chief function in the body is to increase the
availability of energy in the form of glucose. Both hormones may prove relevant
to MDMA’s role in psychotherapy: Oxytocin may strengthen the bond between
therapist and patient, and cortisol could contribute to “unlearning” the fear
responses that normally prevent patients from grappling with painful topics.
MDMA’s method of looting the brain’s pleasure treasury is also its downfall.
Afterward, the brain must rebuild its stores from scratch, and many users exhibit
some signs of depression, irritability, or lethargy a few days after their trip.
Others, however, experience no such moody hangover, basking in the golden
afterglow until their feet return to solid ground.
[ TOXICITY ]
Media reports tend to sensationalize every MDMA-related death, in stark
contrast to the many deaths caused by alcohol or tobacco. In reality, MDMA has
fairly low toxicity when used in moderation. Considering the millions of users
who have tried it, the relatively few medical emergencies and fatalities—while
unquestionably tragic—pale in comparison to other commonly accepted vices
and refute MDMA’s image as a toxic poison.
Used carelessly, however, MDMA can be very dangerous. Because of its
dramatic effect on brain chemistry, MDMA exhibits rapid tolerance and
produces withdrawal effects in regular users who quit suddenly. Dosages are not
as forgiving as with psychedelics such as psilocybin mushrooms or LSD, and
serious overdoses do occur. For some people, no dose is safe. In particular,
because MDMA increases heart rate and blood pressure, it is not recommended
for those with heart conditions. Others just react poorly, complaining of tense
muscles, anxiety, and excessive sweating. Overall, though, more than 97 percent
of users place a positive value on the experience afterward.
One major concern debated for decades is neurotoxicity. Early studies were
conducted on animals, not humans, and with massive doses that did not correlate
to typical therapeutic or recreational amounts. Nevertheless, claims of MDMA’s
neurotoxicity gained traction in the media and the popular consciousness and
played a large role in its prohibition.
There was some truth to the claims. Later studies with humans have shown
that frequent high doses of MDMA are, in fact, neurotoxic, but moderate doses
do not appear to correlate with any kind of brain damage or lasting impairments.
Chronic heavy users may develop structural changes to the serotonin-based
neural pathways, depleted serotonin, and death and damage to neurons in key
brain regions. They may show cognitive impairments and poor memory and
suffer from insomnia, depression, or anxiety. The good news is, for people who
use only moderate doses a few times a year, no such negative trends have been
found.
In spite of what headlines may say, most deaths and medical emergencies
attributed to MDMA are not overdoses. The main concerns are dehydration and
heatstroke, usually as a result of dancing for hours in a hot environment without
properly hydrating. MDMA can contribute to heatstroke by raising the body’s
temperature and interfering with normal temperature-regulation processes, but
heatstroke is fairly common, even among clubbers who have not taken drugs.
Education and preparatory measures, including proper air-cooling and plentiful
water provided by event organizers, can help prevent this.
Several nonprofits and advocacy groups around the globe are seeking to
change the approach to recreational MDMA use by focusing on “harm
reduction” efforts. One method is pill testing, a service offered at progressive
events such as Boom Festival in Portugal to provide attendees with real-time
information about their substances. As long as MDMA remains an unregulated
black market drug, pill testing will be an essential—and potentially life-saving—
public health service for the millions of people who consume it.
[ RESURGENCE OF RESEARCH ]
Although it remains a strictly controlled substance, a resurgence of interest has
brought MDMA back to the forefront of psychiatry in recent years. Before its
prohibition, a couple of studies provided tantalizing clues about the compound’s
medical potential. Participants of one study reported lasting improvements in
their personal relationships, deeper insight into personal problems, and an
“expanded mental perspective.” Subjects also felt that “their defenses were
lowered”—a key component of the therapeutic process.
Another study, conducted by a Swiss team led by Dr. Peter Gasser, examined
the long-term effects of 121 patients who had undergone several MDMA-
assisted therapy sessions. More than 80 percent reported enhanced quality of
life, and over 90 percent experienced an improvement in the condition for which
they had sought therapy. Respondents also indicated a decrease in using drugs
such as alcohol and cannabis.
After its prohibition in 1985, MDMA research lay dormant for a time, but in
the last decade, it has returned in full force. MAPS is now investigating MDMA-
assisted therapy as a potential cure for PTSD, as well as for social anxiety in
autistic adults and anxiety in people with terminal illnesses. MAPS president and
founder Rick Doblin estimates that, by 2021, MDMA will be approved as a
prescription treatment for PTSD in the United States. This is an ambitious goal,
but MAPS has made considerable headway. In a pilot study, more than 80
percent of subjects no longer met the criteria for PTSD after their sessions—an
incredible recovery rate for such a challenging and intractable condition.
Medical MDMA is groundbreaking in many ways. First, its effects are unique
in the field of psychiatry—nothing even remotely similar has ever gotten so
close to becoming a mainstream medicine. Most medicines prescribed for mental
disorders such as PTSD and anxiety are “maintenance drugs” that must be taken
every day. Usually, these treat the symptoms rather than the underlying causes,
and they frequently cause unpleasant side effects while only partially resolving
the condition.
In stark contrast, MDMA only needs to be taken once or twice—in the
presence of specially trained therapists—to produce lasting benefits. According
to researchers, that’s because MDMA opens subjects up to their own “inner
healing intelligence,” allowing them to process traumatic memories instead of
merely numbing them. MDMA-assisted therapy is a far cry from your average
visit to the shrink. Not just a new medicine, MDMA offers an altogether new
healing modality, where patients take the medicine in the presence of two trusted
therapists in a calm and relaxing office setting.
What’s the light at the end of the tunnel? The rehabilitation of MDMA as a
valuable medicine and the opportunity to offer healing to the people who need it
most—veterans, firefighters, police officers, victims of sexual assault, and others
recovering from severe trauma. Perhaps, then, MDMA will have truly earned the
title of the “love drug.”
A SOLDIER’S TESTIMONIAL
In an eye-opening “Ask Me Anything” interactive session on Reddit, retired U. S. Army Sergeant
Tony Macie, an Iraq War veteran, shed some light on his experience with PTSD and MDMA therapy.
Like many with PTSD, his condition had failed to improve after traditional treatments such as talk
therapy. Desperate for help, he enrolled in a MAPS-sponsored study, and the results were astonishing:
…when the MDMA kicked in I felt a wave of relaxation and peace come over me. For the first hour I
did not really talk, I just laid there and enjoyed the quietness of my normally hyper vigilant mind.
…[That’s] when memories started to come up…. If I tried to push them away I would feel anxious, but
if I dealt with it and processed the memory, I would have a wave of pleasure come over my body. I
believe that the MDMA was showing me how to deal with my trauma and also that it is more
beneficial for me to face trauma head on than to try [to] ignore it or suppress it. I had a lot of
powerful realizations that day.
Tony emerged a different man. No longer dogged by constant anxiety and vigilance, he quit all
prescription medications and hasn’t looked back.
“Instead of trying to forget experiences,” he writes, “I focus on learning from them.” MDMA is not
a panacea, and not all PTSD sufferers will respond as positively as Tony Macie has. But he believes
that if research continues to demonstrate positive results, all people with trauma deserve to have this
revolutionary treatment at their disposal.
CHAPTER THREE
DISSOCIATIVE PSYCHEDELICS
The dissociatives, so named because they distance users from their
surroundings and even their own bodies, have medical uses ranging
from anesthesia to cough suppression. Ketamine, the tranquilizer-
cum-club-drug, is emerging as a powerful new treatment for severe
depression. But beware—at higher doses, astral travel and other
bizarre out-of-body experiences prevail.
DXM
DISCOVERED DURATION
Swiss chemists Andre Grüssner and Otto Schnider 4 to 8 hours
in 1946
BEST KNOWN AS the main ingredient in most cough medicines
FIG. 3.1
DEXTROMETHORPHAN
[ THE EXPERIENCE ]
Dextromethorphan was developed as a synthetic opioid analog, but its effects are
nothing like morphine and other opioids. In fact, it’s more akin to dissociatives
such as ketamine and PCP. At low doses, dissociatives produce euphoria,
anesthesia, and unusual bodily sensations. At higher levels, they can induce
profound out-of-body experiences.
Among DXM enthusiasts, the experience is often divided into four stages or
“plateaus.” It’s not merely the intensity that changes as the dose goes up, the
effects change completely. At the lower plateaus, it’s a stimulant with euphoric
effects; at higher doses, it’s a full on dissociative anesthetic, equally capable of
producing sublime out-of-body experiences and episodes of temporary
psychosis.
The music totally pulled me in. I could no longer feel my body or the
headphones. I felt like I was in some strange video game, flying over
computer generated terrain. I often felt like I was in a huge concert hall
listening to the music come from all around me. I was always in control,
though. If I opened my eyes I could return to “reality.”
…is totally unlike the euphoria from “body drugs” such as cocaine or
heroin, and equally unlike the euphoria from MDMA (Ecstasy). Instead, it
is a sensation of being totally at peace with oneself, the universe, and other
people. Ordinary cares and concerns seem to vanish as one enters a world
where anything is possible, and the body becomes increasingly irrelevant.
The second plateau intensifies the effects of the first, but adds some new
features, such as closed-eye visual hallucinations and distortions to the fabric of
time and space. The user becomes much more isolated from her environment,
but is still coherent enough to interact with it. The senses start to flicker, as
though all sounds and images are processed through a strobe light. Walking,
dancing, and spinning become unusually pleasurable, thanks to physical
sensations that mimic free-fall or low gravity.
Lower doses can also have empathogenic effects. Users often report a sense
of empathy and openness that allows them to revisit old memories and confess
secrets that would normally be too embarrassing to admit. Though likely less
effective than MDMA in therapeutic contexts, this aspect of the DXM
experience should not be overlooked. Therapeutic results may be limited by the
compound’s effects on memory: The higher the dose, the less one is likely to
remember of the experience.
But all is not warm and fuzzy. Higher plateaus frequently lead to delusional
thinking, and brushes with psychosis are common. Although DXM is not
particularly addictive, users who drink too deeply and too often from the trough
of DXM consciousness run the risk of psychological addiction and other
potential mental harms. Although relatively safe in the short term, the long- term
consequences of DXM overuse are not well understood.
Gradually, these shifting forms were taking on more substance. They were
coalescing into life forms; entities really—spectacular, bioluminescent,
massy things that churned like thick, boiling, liquid…. Some were like
complex blobs, jellyfish, or worms with thousands of pseudopodia. All were
constantly writhing and huge. I could sense they were intelligent.
…I never felt as if I were in danger. These things seemed not only friendly,
but affectionate…. Their appearances were not monstrous so much as
stunningly beautiful.
I felt as though I had a connection with God, one that I had never before
had…. The upper plateaus are most definitely meant for spirituality. I was
being cradled by God as he protected me from myself. I was comforted,
more than I ever had been before.
Unpredictable and often challenging, the substance is one to be respected, perhaps even feared.
FIG. 3.2
(RS)-2-(2-CHLOROPHENYL)-2-(METHYLAMINO)CYCLOHEXANONE
In the meantime, its appeal grew among veterinarians, who found in ketamine
a safe and reliable anesthetic for a wide range of animals. It also became the top
anesthetic in developing countries that lack resuscitation technology because it
can be administered without slowing the heart or lungs. For regions with
sophisticated health systems, however, its use has generally been limited to
children and trauma patients, for whom alternative options may be too risky.
What prevented this purpose-built chemical from becoming the go-to
medicine for all anesthetic needs? Its downfall was the emergence delirium that
plagued postoperative patients with hallucinations and uncomfortable sensations.
It turns out people getting surgeries prefer not to begin their recovery with a
disturbing out-of-body experience.
But when it comes to using substances, humans are endlessly creative and
motivated by many end goals. What the physician considers an undesirable side
effect is regarded by psychonauts as the main event. Indeed, for some, the
ketamine headspace represents the apex of all possible consciousness
experiences. Anesthesia’s loss is psychedelia’s gain: Ketamine owes its enduring
popularity among ravers and consciousness explorers to the same qualities
doctors struggle to suppress.
Nevertheless, because of its safety profile and ease of administration, it is still
considered a staple drug in medicine. The World Health Organization lists it as
one of its “essential medicines,” the fundamental drugs that hospitals across the
world must stock to meet the basic needs of their patients. And in veterinary
clinics, ketamine remains the primary anesthetic for all species. Apparently, no
one is worried about Lassie suffering from a postoperative dissociative episode.
[ THE EXPERIENCE ]
The synthesis of ketamine is quite complex, so the black market supply is most
often diverted from legitimate sources—often pharmaceutical companies in
India or Mexico—rather than produced in clandestine labs. It is typically snorted
as a white powder. In liquid form, it can also be injected into a muscle or, less
commonly, directly into a vein. By injection, the ketamine experience is shorter,
more intense, and comes on more quickly.
Edward Domino, who conducted the first human trials of ketamine, was
unsure how to characterize the substance. When the professor described the
“disconnection” felt by his research subjects to his wife, Toni, she suggested the
term “dissociative anesthetic.” The name has stuck.
For millions of people, ketamine represents the definitive dissociative
experience. At low doses, it can be stimulating and even sociable, as many
thousands of clubbers and ravers can attest. Physical sensations also change—
the sense of proportions of one’s body can shrink or elongate, coordination is
compromised, and movements take on a “bouncy” quality that encourages
sweeping, exaggerated gestures. A survey of ketamine users found that their
favorite aspects were hallucinations, giddiness, out-of-body experiences, and
“melting into the surroundings.” With a push of energy, distortions of time and
space, and an indescribable “dreamy” feeling, many find it ideal for a night out
dancing.
Care must be taken not to overindulge, however, or a partygoer is liable to
wind up on the floor, uncommunicative, while his astral form roams the cosmos.
At higher doses, the trip becomes deeply introspective. This dosage precludes
any coherent connection with reality and is completely incompatible with the
dance scene. Those who choose to venture this far opt for more private
environments.
JOHN C. LILLY
Neuroscientist, author, and psychedelic enthusiast John C. Lilly was a man of many interests and wild
ideas. A lifelong explorer of consciousness, Lilly never hesitated to dive headfirst into any subject that
piqued his boundless curiosity, even when that meant using his own mind as an experimental
laboratory.
Dedicated to his work and more than a little eccentric, Lilly fit neatly into the popular archetype of
“mad scientist.” He is perhaps best remembered for his research with dolphins, who he believed could
communicate with humans—if only we could decipher their unique language of squeaks and clicks.
But Lilly was also an avid explorer of inner space, exemplifying the term “psychonaut” long before
it gained popular currency. He invented the isolation tank—a totally enclosed sensory-deprivation
chamber filled with buoyant, body-temperature water. Designed to remove all sensation of sight,
sound, and touch, the isolation tank separates the mind from the physical self, producing a substance-
free form of dissociation.
Lilly also experimented with high doses of LSD and ketamine, documenting the results in several
autobiographical books. He often combined these chemical experiments with his other research
interests, spending many hours telepathically communicating with dolphins or exploring the
seemingly limitless bounds of his mind while floating in one of his tanks.
Lilly became an alarmingly frequent user of ketamine, occasionally injecting it every hour for days
at a time. He claimed the substance provided a window into other realities:
On K… I can open my eyes in this reality and dimly see the alternate reality, then close my eyes, and
the alternate reality picks up. On K you can tune your internal eyes.
On two different occasions, he nearly died from reckless overuse of the substance, and he began to
elaborate bizarre conspiracy theories about cosmic entities who interfere in human affairs. In spite of
his excesses—or perhaps because of them—his books gained a significant readership and exposed
ketamine to a broader audience. Today, John Lilly’s writings provide a fascinating insight into the
incredible power, and very real dangers, of a human mind immersed in ketamine space.
The dissociative state shares many qualities with classic near-death
experiences: floating outside the body and observing it from above, transcending
reality and receiving secret insights about the meaning of existence, and having
one’s life “flash before your eyes,” a vivid review of forgotten memories some
people find therapeutic. In spite of the name, a person need not be in any
physical danger to have such a near-death experience.
One of the most fascinating connections is the appearance of spiritual
connotations in both ketamine and near-death experiences, even in nonreligious
people. Travelers to deep inner space sometimes speak of surrendering to God,
entering a bright internal light, or falling through a formless void, where they
become filled with an ineffable sense of serenity and oneness.
Ketamine did not really become popular outside the field of medicine until the 1990s when it
exploded onto the clubbing and rave scenes.
Altogether more than a thousand alcoholic patients have been treated with ketamine without any
lasting adverse reactions.
Of ketamine’s many promising new uses, the most notable is for depression.
A host of studies reveal that a single low dose of ketamine reduces depression
within hours, even in those who have not responded well to talk therapy,
antidepressants, or other medications. Relief lasts up to a week. Suicidal
tendencies are also greatly reduced. Researchers are unsure how ketamine
induces such long-lived benefits, as the active compound is eliminated from the
body in a matter of hours.
These early and somewhat surprising results suggest ketamine may offer
benefits for a wider variety of clinical applications than anyone had previously
guessed. If this humble tranquilizer continues to astound, it will be a very long
time before our understanding of it is complete.
NITROUS OXIDE
DISCOVERED DURATION
Joseph Priestley in 1772 Less than 5 minutes
ALSO KNOWN AS laughing gas
FIG. 3.3
N2O
[ THE EXPERIENCE ]
One good lungful provides a 30-second experience characterized by instant
euphoria, dissociative sensations of detachment, and distinctive, echoing audio
distortions often described as “flanging.” Tingles run through the body, and users
often become lightheaded and lose their balance. Higher doses can lead to out-
of-body experiences and fully immersive hallucinations, but rarely last longer
than a couple minutes.
It’s especially common at music festivals, where seated circles of youths pass
around brightly colored balloons filled with the gaseous elixir. About one in
twenty Americans has tried N2O at some point.
One compelling report of the experience comes from a most unlikely source.
Eight years before he became prime minister of the United Kingdom, Winston
Churchill was searching for a friend’s house in New York City. Accustomed to
the left-hand drivers of London, he looked the wrong way when crossing Fifth
Avenue and was hit by a passing car. In the hospital, he was administered nitrous
oxide.
Churchill did not enjoy the process. By his description, the trauma of the car
crash almost seems preferable:
With me the nitrous-oxide trance usually takes this form: The sanctum is
occupied by alien powers. I see the absolute truth and explanation of
things, but something is left out which upsets the whole… This almost
breaks mortal comprehension. It is beyond anything the human mind was
ever meant to master.
For others, this “depth beyond depth” of truth is one of nitrous oxide’s best
features.
But those who’ve delved the deepest—from Sir Humphry Davy to William
James—remark on the ineffable, metaphysical breadth of the nitrous experience.
When he discovered nitrous oxide in 1772, the English chemist Sir Joseph
Priestley was no stranger to science. Though most famous for the discovery of
oxygen, he made a variety of contributions to philosophy, chemistry, and
electricity. To top it off, he even invented a novel method of carbonating water.
But although he enjoyed the refreshing taste of soda water, he was never tempted
to sample his other gaseous creations. The discovery of nitrous oxide’s
psychoactive properties would have to wait for more adventurous—or reckless
—explorers.
In 1799, a physician named Thomas Beddoes established a medical research
facility in Bristol, England, dedicated to treating patients with medicinal gases.
He called it the Pneumatic Institution, and as its superintendent he hired
Humphry Davy, a brilliant young chemist and inventor.
Nitrous oxide became a prime focus for Davy and the Pneumatic Institution.
Unlike Priestley, Davy had no qualms about inhaling novel gases—that was,
after all, the whole point of the Institution. Davy imbibed nitrous oxide with a
passion that others reserved for more common inebriants such as alcohol,
tobacco, and opium and eventually became addicted to it. “I have often felt very
great pleasure,” he wrote, “when breathing it alone, in darkness and silence,
occupied only by ideal existence.”
[ THE PNEUMATIC INSTITUTION ]
In its early days, nitrous oxide attracted not dentists and surgeons, but creative
and curious spirits—poets and philosophers, as well as scientists and inventors.
Enamored with the novel state of mind he had uncovered, Davy introduced
laughing gas to many of his contemporaries, including James Watt, Peter Mark
Roget, and the Romantic poets Robert Southey and Samuel Taylor Coleridge.
Davy began hosting what might be called the first-ever psychedelic parties, and
his circle of friends offered their impressions of this unique inebriant.
After extensive experimentation with the gas, Davy penned a six hundred-
page tract collecting the results of his intense and frequent experiences.
Published in 1800, the book included subjective reports from many of those who
passed through the Institution’s doors. Samuel Coleridge described the high as a
“pleasurable sensation of warmth over my whole frame, resembling what I
remember once to have experienced after returning from a walk in the snow into
a warm room.” Peter Mark Roget was less descriptive. “I felt myself totally
incapable of speaking,” he said—a striking sentiment, coming from the man who
would later pen the quintessential writer’s tool, Roget’s Thesaurus.
James Watt is best known as the namesake of the unit of electrical energy, the
watt, and inventor of the steam engine that made the Industrial Revolution
possible. But he also made a unique contribution to the Pneumatic Institute,
designing a portable version of Davy’s inhalation chamber to facilitate easier
consumption.
In the course of their experiments, Davy and Dr. Beddoes made a prescient
observation. Noting that cuts stopped hurting while intoxicated with nitrous
oxide, they surmised the gas had painkilling properties. Davy correctly predicted
its use as a surgical anesthetic, but, as usual, he was ahead of his time—the
medical world took another forty years to catch on.
FIG. 3.4
SALVIA DIVINORUM
[ ORIGINS AND BACKGROUND ]
MONG PSYCHOACTIVE PLANTS, SALVIA DIVINORUM is utterly unique. Though it’s
A a member of the mint family and a close relative of common sage, salvia—
or “diviner’s sage,” as its Latin name translates—packs far more of a punch
than these kitchen staples. In fact, its active ingredient, Salvinorin A, is the most
potent psychoactive compound in all of nature. It’s often classed as a
dissociative alongside ketamine and DXM, but its effects stand in a league of
their own.
A striking example of the power of cultural beliefs, salvia means two very
different things to the two cultures where it is encountered. To the Mazatec, an
indigenous people based in the mountains of southern Mexico, salvia is a
treasured plant spirit who imparts healing knowledge to learned shamans. It has
a long history of use and is approached with utmost respect to ascertain answers
to important questions. Because it is usually made into a water infusion, and
never smoked, it induces a serene trance state that lasts for 1 or 2 hours.
To modern Western users, who first encountered this peculiar plant in recent
decades, salvia represents little more than a novelty. Though there is a handful of
salvia devotees who use it as a spiritual tool, the plant is usually sought for its
unique high in the name of simple curiosity. It’s even been marketed as a
marijuana substitute, but, in reality, the two plants have little in common other
than being psychoactive and green.
In recent years, salvia has emerged as the unlikely star of a number of online
videos featuring teenagers smoking a highly concentrated form of the herb and
then stumbling over furniture while slurring words or laughing uncontrollably.
It’s fair to say the typical American approach to salvia is both more intense and
less informed than that of their counterparts south of the border. As a result, it
has earned a negative reputation in the media and in the minds of concerned
parents—a fact that would shock the Mazatec shamans who have passed
knowledge of this sacred plant down for countless generations.
The seer’s sage would have to wait several more decades for its day in the
sun. In 1962, mycologist R. Gordon Wasson and chemist Albert Hofmann
returned from Oaxaca with the first ever-flowering samples of the shrub. Their
colleague and botanist Carl Epling identified it as a new species, dubbing it
Salvia divinorum—the diviner’s sage.
[ THE EXPERIENCE ]
The salvia experience features some of the typical dissociative effects, such as
profound distortions of one’s sense of self and what constitutes reality, but
ultimately it stands in a class of its own. Though it offers powerful visual and
bodily hallucinations, they are not remotely similar to those of classical
psychedelics such as LSD or psilocybin mushrooms. Far from euphoric, the
salvia headspace tends to be bleaker and more disturbing than the more popular
psychedelics. But for a select group of devotees who celebrate the plant’s placid
and even spiritual effects, there is no better “plant teacher” than Salvia
divinorum.
Physical sensations such as pulling, stretching, or flying are common. Users
frequently feel as though they are sinking into the furniture, or even falling
through the floor altogether, watching it drift away as they descend into ever-
stranger realms. Salvia fiddles with fundamental levers in our brain’s sense of
identity: People often report merging into nearby inanimate objects, discarding
their human forms like snakeskins as they embrace their new—albeit short-lived
—lives as chairs, walls, or carpets.
Common themes include tunnels and spirals, with people often feeling like
reality itself is peeling apart. Occasionally, salvia offers contact with “entities” or
spirits who may guide the user through the experience.
Seconds after smoking the potent leaves, it’s easy to forget one has taken a
substance at all, and all preconceptions—relationships, histories, names, all the
things that make us human—sink away, replaced by the inexplicable realization
that this is reality now. For a few short minutes, the user remains lost in these
rarefied corridors of consciousness. Then, thankfully, sobriety returns, and, along
with it, one’s sense of self—miraculously intact.
On Erowid, the online drug library, a user going by Temicxoch does an
admirable job of wrangling the ineffable experience into words:
I closed my eyes and lost all sense of my physical self. I roared through a
void. I was surrounded by a space of myriad expanse, yet there was nothing
there. I was exploding in all directions at once, expanding, twisting
outward, yet there was nothing through which to be moving. I flew, I
floated, I flourished. The dark matter which filled me and which I
encompassed sang with energy. Just as the abyss about me had a form, so
its silence was an ecstatic polyphony. My senses rang with delight.
For some, the experience can feel “more real than reality,” and people
sometimes emerge from the salvia spell with the impression that a veil has been
temporarily lifted. The unsettling conclusion—that one’s whole life has been
nothing but a dream, or a simulation—sometimes leads to an existential freak-
out or identity crisis. Thankfully, these feelings usually wear off on their own.
Far from euphoric, the salvia headspace tends to be bleaker and more disturbing than the more
popular psychedelics.
Like other powerful psychoactive substances, salvia can leave some users
with lasting feelings of anxiety and must be approached carefully. Yet, because
of its decidedly noneuphoric effects, it has a very low risk of dependence. In
fact, its effects on the brain are the exact opposite of those that light up our
“reward network,” such as cocaine and methamphetamine.
For the vast majority of people, salvia usage tapers off naturally—after a
strong first dose, many swear it off for good. The herb’s self-regulating nature
has probably helped it remain legal in cultures where most intoxicants, aside
from alcohol and tobacco, are vehemently suppressed.
And yet, even this is changing—in the wake of media attention highlighting
examples of careless use, tolerance for the plant has waned. Though federally
unregulated, salvia is now illegal in a majority of states, making it the latest
victim of the war on inebriants and visionary medicines begun by the first
colonists of this continent.
Meanwhile, in Oaxaca, the diviner’s sage lives on as a vital component of
daily life—a balm for many ailments, a source of answers in times of
uncertainty, and a dose of serenity in a world of chaos. It’s hard to believe that
American commentators and Mazatec shamans are speaking of the same plant.
CHAPTER FOUR
UNIQUE PSYCHEDELICS
The psychedelic misfits, united not by what they have in common, but
by how they stand apart. From the speckled Amanita mushroom in
snowy Siberia to the green “ganja” of Indian mystics; from
intoxicating honey gathered from towering Himalayan cliffs to
sponges growing at the bottom of the sea—these substances are
among the strangest known to man.
AMANITA MUSCARIA
DISCOVERED DURATION
Known to Siberian shamans for millennia; first 6 to 8 hours
discovered by Europeans in the early 1700s
ASSOCIATED WITH traditional Siberian cultures
KEY COMPOUNDS muscimol, ibotenic acid
FIG. 4.1
AMANITA MUSCARIA, OR FLY AGARIC
[ ORIGINS AND BACKGROUND ]
MANITA MUSCARIA, OR FLY AGARIC, BOASTS what may be the most conspicuous
A and iconic appearance of all psychoactive life forms. Gathered in quaint
bunches under evergreens or birches, Amanita’s bright red caps sprinkled
with white polka dots form an unmistakable, almost surreal, image. One almost
expects to see garden fairies flitting about this idyllic scene, but, of course,
they’re not likely to appear until after the mushroom is consumed.
Over the centuries, Amanita muscaria has emerged as pop culture’s
archetypal mushroom, making an appearance in everything from gnome-laden
garden ornaments and kitschy knickknacks to videogame power-ups and
children’s books. Two of Disney’s classic films, Fantasia and Snow White,
feature the iconic mushroom in scenes of lively dancing, reminiscent of its
traditional use among Far Eastern shamans.
The mushroom’s enduring popularity in modern times probably owes more to
its striking appearance and global distribution than its mental effects. It’s
doubtful whether something as innocuous as the Smurfs’ toadstool houses
represents a deliberate allusion to drug-induced visions. Nevertheless, its
association with magic, fairies, and spirits persists to this day.
…the poorer sort… post themselves, on these occasions, round the huts of
the rich, and watch the opportunity of the guests coming down to make
water, and then hold a wooden bowl to receive the urine, which they drink
off greedily… and by this way they also get drunk.
The potency of any given cap depends upon the region and season in which it was harvested.
The division did not always fall between economic classes. In Western
Siberia, only the shamans were permitted to eat the mushrooms; other tribe
members would consume the shaman’s potent urine. In this way, the shaman
became both a literal and figurative conduit, channeling the mushroom’s divine
power for his people.
This seemingly bizarre practice was, in fact, quite practical. In the tundra,
ingesting urine served as a way to conserve a precious resource. Indeed, because
the human body metabolizes the mushroom’s ibotenic acid into the more potent
muscimol, the user’s urine is said to exceed the strength of fresh mushrooms and
even filters out some of the less desirable side effects.
For those who can stomach it, the process can be repeated four or five times
before losing its potency altogether. By repeatedly recycling the active
compounds, a handful of mushrooms can inebriate many people and extend their
altered state for days at a time. If A. muscaria is a gift of the gods, as the
Siberian shamans believe, it’s truly a gift that keeps on giving.
Humans are not alone in eating the fly agarics. Reindeer, too, have a special
taste for them. The Sami people in Finland, noticing the animals’ predilection for
the magical fungus, have been known to collect reindeer urine and drink it for
psychoactive effects.
The fly agaric was revealed as a vital sacrament among a variety of peoples who lived thousands
of miles apart.
…the most attractive gardens where only pleasure and beauty seemed to
rule. Flowers of different colours and shapes and odours appeared before
my eyes; a group of most beautiful women dressed in white going to and fro
seemed to be occupied with the hospitality of this earthly paradise. As if
pleased with my coming, they offered me different fruits, berries, and
flowers.
[ THE EXPERIENCE ]
As a deliriant with remarkable lucidity, a dissociative with tactile and sensual
enhancements, and a sedative that grants the user overwhelming strength and
endurance, A. muscaria is a mushroom of bold contrasts, defined more by its
paradoxes than by any consistent effects. Perhaps the oxymoron of “waking
dream” describes it best. Moments of terror bleed into fits of ecstasy, and a
person may drift from a fevered drumming session into deep sleep without
warning.
Nausea, muscle twitches, and profuse sweating and salivation are the most
common side effects, but these vary widely with the dose and the person. Vision
becomes blurry and coordination is impaired, yet the Koryak say feats of skill
and extraordinary strength are common among mushroom-addled tribesmen.
The mushroom’s unpredictability has surely contributed to its legendary
reputation as a conduit of the gods.
A researcher who spent two years with Siberian tribes described how the men
entered fits of ecstasy after taking the sacrament:
They suddenly sprang raving from their seats and began loudly and wildly
calling for drums…. And now began an indescribable dancing and singing,
a deafening drumming and a wild running about… during which the men
threw everything about recklessly, until they were completely exhausted.
Suddenly they collapsed like dead men and promptly fell into deep sleep.
FIG. 4.2
CANNABIS SATIVA (SHOWN), C. INDICA, AND C. RUDERALIS
Why burn the material to cinders when a precise 350° F (76°C) will do?
If you can eat it and smoke it, why not drink it? As cannabinoids dissolve
readily in alcohol, it’s only natural that enterprising mixologists have begun
crafting cannabis-based tinctures and cocktails. The simplest, sometimes called
the “Green Dragon,” consists of ground cannabis dissolved in high-proof
ethanol, then strained to remove all solids. Most recipes pack a serious wallop: A
few droplets on the gums can keep a person high all day.
[ THE EXPERIENCE ]
Neither a stimulant nor a depressant, cannabis casts a unique spell on the body
and mind. Physically, dry mouth and increased heart rate are typical. The
muscles relax and, as just about everyone knows, the eyes redden.
For most people, the draw of cannabis lies in its intriguing mental effects. The
main highlights are euphoria and relaxation. Every pleasant sensation becomes
more pleasurable—food is more delicious, music becomes exhilarating, and sex
is sublime. Some people feel more social under the influence, and cannabis is
even being investigated as a treatment for social anxiety.
It’s not all good news, however. Some people become anxious and paranoid,
even on low doses. Though some negative reactions may be chalked up to a
high-THC strain or poor setting, it’s safe to say cannabis doesn’t agree with
everyone.
Typically presented in pop culture as a “stoning” drug that dumbs down the
user, cannabis’s real effects are more subtle, especially for those seeking more
than a recreational high. Many people cite improved creativity and imagination
as a primary motivation for indulging. Freed from its usual routes, one’s train of
thought traces unexpected paths across the mental landscape. Mundane thoughts
and situations become hilarious; truisms and non sequiturs are transformed into
nuggets of wisdom.
Although true hallucinations are rare at typical doses, perceptual changes are
common. These can range from vibrant scenes imagined behind closed eyes to
distortions of time, space, and one’s own body. It’s not an experience prone to
sudden, dramatic epiphanies but rather serene and contemplative states of being.
As a substance that frequently occasions a sense of deep connectedness, wonder,
and imagination, its classification as a mild psychedelic seems completely
appropriate.
[ THE RASTAFARI ]
Today, the Rastafari are one of the best-known examples of religious cannabis
use. Founded by Jamaicans in the 1930s after the coronation of the Ethiopian
emperor Haile Selassie, the Rastafari movement accepted the emperor as God
incarnate. The Rastafari combine this view with traditional Christian principles,
such as the divinity of Jesus, and, of course, the appreciation of cannabis as a
sacrament and way of life.
Cannabis is central to the Rastafari way. A Rasta smokes ganja when he needs
spiritual counsel from Jah—the Rastafari term for God—and also in communal
settings. Rastas come together for “Reasoning” sessions, where adherents smoke
the herb from a long-necked water pipe called a chalice, meditate together, and
debate the best ways to apply their values to everyday life. The Rastafari not
only believe that cannabis improves mental clarity and fosters peace, but that its
use is divinely sanctioned. They see references to cannabis in the Bible, for
instance, the Tree of Life is believed to refer to cannabis and likewise the
scripture from Revelation 22:2: “The herb is the healing of nations.”
For many people, awareness of the religion came in the form of reggae music.
In particular, Bob Marley, the world-famous reggae icon and unabashed cannabis
smoker, did much to popularize the movement. Marley’s music was deeply
affected by his spiritual values, and his seventy-five million sold records—and
counting—continue to spread the Rasta way far beyond the borders of Jamaica.
The Rastafari not only believe that cannabis improves mental clarity and fosters peace, but that its
use is divinely sanctioned.
[ HEALING HERB ]
For a plant classified by the federal government as having “no currently accepted
medical use,” cannabis boasts a surprising range of potential medical
applications. One may turn out to be chronic pain relief. States with medical
marijuana laws show a significant drop in painkiller prescriptions, as well as
reductions in hospital admissions relating to opioid abuse and dependence,
indicating many people find cannabis preferable to opioids in managing pain.
Compared to opioids such as morphine and codeine, cannabis has more
agreeable side effects and a lower risk of dependence.
Cannabis is also more effective at treating neuropathic pain (pain caused by
nerve damage) where opioids offer little help. In a nation ravaged by opioid
addiction, which, according to the CDC, kills more than thirty thousand people
per year, an effective painkiller that reduces opioid use should be celebrated as a
godsend and prioritized for further study.
The plant can also be used to treat neurological problems, including epilepsy
and multiple sclerosis (MS). A study of MS patients showed that cannabis
helped reduce their muscle spasms as well as other symptoms of the disease such
as overactive bladder and painful sensations. Pure CBD, one of the plaint’s main
cannabinoids, has been shown to reduce seizures, even in the most treatment-
resistant forms of epilepsy.
The increased appetite, colloquially known as “the munchies,” is utilized by
some people to help combat eating disorders. This, combined with its antinausea
properties, has made it an ideal substance for both chemotherapy patients and
those with AIDS, who often have great difficulty eating.
Cannabis is also a powerful anti-inflammatory. As inflammation is such a
common component in many diseases, cannabis may have beneficial effects on a
wide range of conditions including Crohn’s disease, atherosclerosis, rheumatoid
arthritis, inflammation associated with certain cancers, and—somewhat
surprisingly, for a substance most often smoked—asthma.
The list continues. By reducing internal eye pressure, cannabis may prove
useful in treating glaucoma. And early research suggests THC and other
cannabinoids can target brain cancer cells, shrinking tumors in mice.
The herb is good for more than just bodily complaints. Its effects on
consciousness have found favor among people with PTSD, and its anxiety-
reducing effects are famous. Some people claim a mood-stabilizing effect, and
early research indicates it may help relieve stress-related depression.
[ HEALTH PROBLEMS ]
Cannabis is not a miracle cure, however. Most of its medical benefits remain
anecdotal or speculative, and it does have real side effects. Some people
complain of dizziness, fatigue, vomiting, and even hallucinations. Long-term
use, though far safer than common drugs like tobacco and alcohol, has its share
of problems. True to the “stoner” stereotype, chronic heavy users have a higher
risk of depression, tiredness, and a general lack of motivation.
Formulations with THC can negatively affect memory and thought processes,
producing a mental fog that only abstinence can lift. Though claims that it makes
people crazy are vastly exaggerated, cannabis can induce psychosis in people
predisposed to schizophrenia and may hasten the onset of the disease.
Although cannabis smoke includes many of the same toxins and carcinogens
as tobacco smoke, no definitive link between moderate smoking and lung cancer
has been discovered. Though there may be a limited correlation, it’s clear any
lung damage from cannabis pales in comparison to that of tobacco.
These results puzzled researchers and medical experts, who suggest that
cannabis smoke may contain antioxidant and other protective components that
counteract the harmful effects of the carcinogens. That’s not to say smoking
cannabis is perfectly safe on the lungs—heavy smokers may experience reduced
breathing capacity and lung inflammation that can cause asthma-like symptoms
after many years. Vaporizing greatly reduces these risks.
[ SHIFTING ATTITUDES ]
The twentieth century was not kind to cannabis, but it’s finally getting its day in
the sun. Many countries in Latin America and Europe have decriminalized the
possession of small amounts, including Portugal, Spain, Colombia, Ecuador,
Mexico, Peru, and Chile. Jamaica, home of the Rastafari, finally decriminalized
possession in 2015. Uruguay, recognizing that prohibition fostered a black
market far more toxic than the plant itself, legalized it altogether in 2014—the
first country to do so. In the Netherlands, “coffeeshops” have been serving up
bud since the 1970s, though it remains technically illegal.
Even Americans are coming around. Legalization is now supported by a
majority of Americans and has become something of a rallying cry for many
political candidates—a stance that would have meant political suicide not long
ago. Pot, the enduring symbol of the counterculture, is officially mainstream.
People in a majority of all states now have legal access to medical marijuana.
Nine states and the District of Columbia (and counting) have fully legalized the
plant, including California—the sixth largest economy in the world. Altogether,
more than seventy million Americans enjoy access to legal recreational
cannabis.
While there has been progress, the US remains in a state of transition. The
federal government has not moved from the position of steadfast prohibition.
Cannabis businesses have been forced to deal in cash because national banks,
fearful of repercussions from the federal government, refused their business.
Until the national laws change, neither business owners nor consumers have any
guarantee the feds won’t come knocking, as they have in countless dispensary
and home raids in the past.
Nevertheless, prohibition is crumbling. With each state that legalizes, the
federal government’s position becomes increasingly untenable. Attitudes and
laws are changing, not just in the United States but around the world.
Most of its medical benefits remain anecdotal or speculative, and it does have real side effects.
DIPT
DISCOVERED DURATION
Alexander Shulgin in 1980 8 to 12 hours, with audio effects lasting up to 36
hours
FAMOUS FOR auditory distortions
FIG. 4.3
N,N-DIISOPROPYLTRYPTAMINE
[ THE EXPERIENCE ]
DiPT can be eaten, vaporized, or insufflated (sniffed). The latter is said to be
incredibly painful, so, although the substance both smells and tastes disgusting,
most users opt to swallow it. With this method, the main experience lasts
between 8 and 12 hours, though the auditory effects can linger for a full 36
hours.
The first hour or two can be physically uncomfortable. The energy rush has
been likened to the onset of MDMA, and the light-headedness and shortened
attention span are common to many stimulants and psychedelics. The bloating,
nausea, and sometimes-painful inner-ear pressure, however, read more like the
side effects list from a pharmaceutical ad.
Then, several hours in—just when the explorer is ready to write off the
substance’s hype as a cruel hoax—the audio effects begin in earnest. Mercifully,
the indigestion often subsides around the same time.
The first alert often comes in the form of an unmistakable shift in one’s
speaking voice—“Is that really what I sound like?” In Shulgin’s TiHKAL, an
anonymous tester describes this bizarre warping:
But DiPT is not merely a helium balloon in reverse, deepening voices instead
of transforming them into cartoonish squeaks. All sounds are affected, especially
those with a well-defined pitch. One amateur musician offers a detailed
description:
Like a warbled tape deck, not all sounds are affected equally. While low tones
tend to get even lower, high pitches instead burst with chirping and stretching
sounds: “Inhaling, it sounds like high-pitched wire tension noises are happening
within that breath.”
But how does it affect music? The results are in, and they’re not pretty.
“Piano sounds like a bar-room disaster,” one early tester told Shulgin.
A more recent experimenter watched a video of a symphony orchestra:
“Predictably enough, it sounded like nobody had practiced and the conductor
was drunk and insane.” Clearly, this is not the substance to take before your
favorite band goes on stage.
Shulgin explained why everything sounds dissonant, even an unaccompanied
solo instrument: “You play an oboe… and it no longer sounds like an oboe
because all the harmonics are out of pitch with one another, no longer
harmonically related.” The delicate tonal balance is destroyed. What’s left is
dreck: “It’s just ugly music.”
Or perhaps not. Others have described profound sonic experiences with the
drug. According to some, the secret is choosing music that’s already dissonant—
it can hardly go out of tune if it’s not in tune to begin with. A bit of garage punk
or minimalist techno, for instance, can transform into something fresh without
becoming unlistenable in the process.
The secret is choosing music that’s already dissonant—it can hardly go out of tune if it’s not in tune
to begin with.
It’s not always “an aural toy box of ear-tickling proportions,” as one
psychonaut put it. The compound’s disconcerting effects on sound are often
accompanied by physical sensations in the ear, as though plugged up by wax.
DiPT users sometimes feel the need to yawn, as though ascending in an airplane,
but find no relief.
This inner ear pressure increases with the dose and can be painful. Tinnitus—
a sometimes disturbingly loud ringing, most noticeable in a silent environment—
is also common. Both symptoms can last for days, or even weeks, afterward,
especially with very high doses. Whether these sensations are related to DiPT’s
pitch-bending effect remains unknown.
…nearly moved to tears by what I heard… [it was] one of the most amazing drug effects I have ever
encountered or probably ever will encounter: the ability to re-experience something beloved as
completely new again… It is something I expect to remember vividly for a very, very long time.
I stepped outside and looked at the sky in awe… The clouds were turning
into balls of fire that resembled meteors and they started falling from the
sky. It was the end of a most incredible night.
These doses are not for the faint of heart. At this level, the audio distortions
become overwhelming and it is nearly impossible to maintain a conversation.
Those looking for visual effects should stick with more traditional psychedelics.
NATIVE TO fish—coastal waters off Africa, Australia, and in the Mediterranean; sponges—the Caribbean
FIG. 4.4
SARPA SALPA (SHOWN), FISHES IN KYPHOSUS, SPONGES INCLUDING S. SMENOSPONGIA (SHOWN) AND S. ECHINA
[ ORIGINS AND BACKGROUND ]
OR MOST PEOPLE, THE PHRASE “NATURAL PSYCHEDELIC” brings to mind a variety
F of plants, ranging from ayahuasca vines to peyote cacti, and a handful of
psychoactive fungi. But all of these are land-based species. Often
overlooked is that vast and enigmatic world that exists alongside ours yet
remains alien to us—the oceans. Water covers 71 percent of our planet’s surface,
but the biochemistry of sea creatures remains relatively unexplored. We have
ample evidence of life’s ingenuity in conjuring intoxicating chemicals on land—
what molecular treasure might lie in the murky depths of the sea?
Our current knowledge provides two fascinating examples of sea organisms
containing visionary chemicals. First, a surprising number of fish species have
been known to cause ichthyoallyeinotoxism, or hallucinogenic fish inebriation.
This is distinguished from other, less trippy varieties of fish poisoning by the
presence of vivid auditory and visual hallucinations that can last for several
days. In some cultures, especially among islanders in Polynesia and the Indian
Ocean, there is an ongoing tradition of intentional fish intoxication. But for the
casual seafood enthusiast, such “trips”—complete with nausea, dizziness, and
disturbing nightmares—are accidental and decidedly unpleasant.
The second example is more recent and has absolutely no history of ritual use
by humans—at least not yet. Among the humble sea sponges, there are species
that produce molecules seen nowhere else in nature—namely, 5-Bromo-DMT,
which has been identified as a likely psychedelic.
The “bromo” refers to bromine. Because bromine is very rare in the earth’s
crust, it almost never appears in the chemistry of land-based organisms. But in
the ocean, bromine is much more common, and at least a handful of sea sponges
have incorporated it into their internal molecular factories. Sponges, it turns out,
are the clandestine chemists of the ocean floor and having churned out unusual
compounds for millennia without attracting notice, very successful ones at that.
[ THE EXPERIENCE ]
People report a variety of symptoms, but frightening nightmares and
hallucinations, poor coordination, blurry vision, disorientation, and impaired
memory are common. Tightness in the chest is another frequent complaint.
Many patients, blindsided by the unexpected onset of such disturbing symptoms,
believe they are dying and start to panic. The nature of the experience appears
inconsistent with classical psychedelics, such as LSD or psilocybin, and may
point instead to a deliriant active compound.
In spite of its unpleasantness, “poisoning” events are not always accidental.
Ancient Romans throughout the Mediterranean were said to consume the fish to
embark on extreme mental voyages. Surely, fish tripping marks one of the most
unusual of the Roman Empire’s many discoveries and strange vices.
Polynesian islanders once incorporated the fish into visionary ceremonies.
The details have been lost to time, but some natives still cook up known
hallucinogenic fish when they feel like kicking back and, well, hallucinating.
Those who enjoy this briny variety of intoxication make no attempt to remove
the fish heads, instead mixing them right into their stews to increase their
potency.
THE MYSTERY OF
DREAM FISH CHEMISTRY
What’s the trippy ingredient that makes some fish hallucinogenic? No one knows. Although episodes
of hallucinogenic fish poisoning are fairly well documented, they’re not at all well understood.
Studies are confounded by the phenomenon’s sporadic nature. Most of the time, fish from affected
species are safe to eat, but in some specimens and some seasons—especially spring and summer—the
danger increases. Symptoms and duration vary, and it’s not always easy to tell when someone has
suffered ichthyoallyeinotoxism rather than another foodborne illness.
Further complicating matters, hallucinogenic poisonings may be caused by many different
compounds, which may vary by species. And then there’s the question of origin—do these fish
produce psychedelic compounds on their own, or, as some scientists have speculated, do they acquire
them from microbes in their diet? Most dream fish are herbivores; the intense but inconsistent effects
may derive from a form of plankton called dinoflagellates, from plants known as seagrasses, or from
seaweeds in the genus Caulerpa.
Sponges are a bit trippy to begin with—although classified as animals, they have no circulatory
systems, digestive organs, or nerves.
I closed my eyes and found myself drifting through the ocean on an ice floe
shaped like a puzzle piece…. Very light and nonaggressive, nonnauseating.
Drugs such as this are aptly described as ‘serenic.’
[ MORE TO DISCOVER ]
There are an estimated 8.7 million species in the world, one-fourth of which are
thought to reside in the oceans. We are still only beginning to understand the
complex ecosystems of those unplumbed depths. And when it comes to
molecular cocktails and defense toxins, perfected by many thousands of aquatic
species over millions of years, we’ve barely scratched the surface—so to speak.
In particular, marine invertebrates provide an abundance of compounds that
resemble serotonin and dopamine—chemical messengers fundamental to human
consciousness and intimately involved in mental illnesses such as depression,
anxiety, and addiction. Yet in spite of their potential as medicines and
entheogens, these undersea chemicals remain almost completely unexplored.
Novel psychoactive substances may hide in the darkness of the ocean’s deepest
corners or perhaps in plain sight among microbes and algae on shallow-water
reefs. What chemical clues lie waiting to be discovered?
IBOGA
DISCOVERED DURATION
Known for centuries in Western Central Africa; first 24 to 36 hours; residual stimulation lasts for days or
discovered by Europeans in mid-1800s weeks
KNOWN AS the sacrament of the Bwiti religion; a potential treatment for addiction
KEY COMPOUND ibogaine
FIG. 4.5
TABERNANTHE IBOGA
[ ORIGINS AND BACKGROUND ]
N GABON, A SMALL COUNTRY ON THE WESTERN COAST OF CENTRAL AFRICA, iboga is
I easy to find—the shrub grows in the wild, and a powder made from its roots
serves as the sacrament and very foundation of the popular Bwiti religion. It
can also be found in a number of luxurious, if unorthodox, detox centers in
various parts of the world, including Mexico, Costa Rica, the Netherlands, New
Zealand, and even Canada. According to its many believers, iboga stops
withdrawal completely and offers a fresh start to people struggling with
addiction. But, in the United States and a handful of other countries, iboga and
its chief active compound, ibogaine, are banned and very difficult to find on the
black market due to their lack of recreational appeal. Advocates for the plant’s
addiction-fighting qualities are eager to change that, but scientific studies have
been slow in coming.
Iboga is a rainforest shrub growing to about 6 feet (1.8 m) in height, with
white and pink flowers and distinctive orange fruits. For spiritual ceremonies
and drug treatment centers, however, the roots are the main attraction. They
contain a mix of many alkaloids, but the strangest and best known is ibogaine.
Ibogaine’s effects on the brain and body are complex: Like psilocybin and LSD,
with which it shares a common structure, it shows activity at serotonin receptors,
which likely explains its more visionary qualities. Unlike those molecules,
however, ibogaine also has strong activity at several other receptor types,
including those utilized by ketamine and salvia to produce their dissociative,
mind-bending effects. It’s unclear how exactly these receptors elicit ibogaine’s
putative anti-addictive properties.
[ BWITI ]
No one knows exactly how long iboga has featured as a spiritual medicine
among indigenous peoples in western Central Africa. In the late nineteenth
century, some of the native Bantu peoples, facing persecution from French
missionaries, fled to the forests. There, they encountered the Babongo, a Pygmy
tribe with secret knowledge of a powerful root, which they shared with the Bantu
visitors. Thus, the Bwiti religion was born, or perhaps remade: a heavily
ancestor-focused tradition that featured iboga as its sacrament in various
ceremonies and rites of passage.
Bwiti has evolved into numerous sects and spread from Gabon into
neighboring countries. The Bantu did not escape the missionaries completely:
Many modern Bwiti traditions combine their roots of animism, iboga journeying,
and ancestor worship with elements of Catholicism. Other groups have
steadfastly resisted outside influences and continue to practice the religion as
their forebears learned it more than a century ago. The Catholic Church has
disavowed the syncretic, Christianized form of Bwiti, but the religion is here to
stay: It’s one of the three official religions in Gabon, and in 2000, the country’s
Council of Ministers declared iboga a national treasure.
Iboga is central to the Bwiti way of life. It is used by the Bantu peoples to
connect with the spiritual realm, diagnose the sick, and to honor—and even meet
—their ancestors. In each Bantu community, the spiritual leader and expert
herbalist, known as the nganga, leads the ceremonies. These elaborate rituals,
which often go on for several days, usually incorporate singing, dancing, and
musicians playing drums, harps, and rattles.
[ THE EXPERIENCE ]
In small doses, ibogaine has a stimulant effect. West African tribes have utilized
the plant in sub-psychedelic doses to stay alert for long journeys and hunting
expeditions.
A large dose, however, provides a profound psychedelic journey. The first
sign is a loud, oscillating tone that pervades the user’s hearing. Some find the
sound distracting or unpleasant, but, in a traditional setting, Bwiti ceremonial
music frequently drowns it out.
A condition known as ataxia quickly sets in: the limbs become rubbery, and
the subject cannot stand or walk steadily. The lack of coordination is heightened
by an intense, motion-sensitive feeling of nausea. Even small movements, such
as turning one’s head, are likely to cause vomiting. Ibogaine also produces
strong photosensitivity, so light becomes painful to bear. With such intense
physical side effects, it’s easy to see why users usually lie down in the dark,
trying to remain completely still—and also why ibogaine has never caught on as
a recreational psychedelic.
The experience is generally split into two phases. The visionary state, lasting
from 3 to 6 hours, consists of vivid waking dreams, memories, and imagined
scenes. Like dreams, they appear laden with surreal and often symbolic content.
People often describe them as fast-moving films or slideshows from one’s past,
including formative childhood scenes rendered in hyper-realistic detail.
Although neither Bwiti practitioners nor drug treatment centers focus on this
aspect, extreme distortions of body image are also common during the visual
stage. According to one user on Erowid, the online library of drug information:
The subject may also encounter one or more “spirits” during this time.
According to Bwiti tradition, these spirits help guide the initiate to the realm of
the ancestors, but such encounters are not limited to the Bwiti ceremonial
context. One user, after describing a harrowing session of “skulls rolling, death,
trees in blossom, all manner of bestial vision,” writes that finally,
The second phase is introspective. Much longer and less visual than the first,
this stage often consists of a “life review” resulting in valuable insights. These
realizations are often related to the imagery from the first few hours.
Between the vividly reimagined life scenes and honest, searing evaluations
that come afterward, seekers are granted a unique opportunity for personal
epiphanies. Perhaps it is this change in perspective combined with the
compound’s withdrawal-stopping effects that allow some people with addiction
to walk away truly changed. This phase can last from 8 to 20 hours, and residual
stimulation lasts for days, or even weeks afterward.
[ BEYOND ADDICTION ]
Some psychiatrists had already adopted ibogaine as a useful substance in
psychotherapy before hearing of Lotsof’s research, but none had discovered its
potential as an addiction treatment. For these therapists, ibogaine served a more
traditional therapeutic role—uncovering repressed memories, shining new light
on deeply held pain and trauma, and providing a new perspective on the
subject’s life and relationships.
When Howard Lotsof met with Leo Zeff, a therapist who had incorporated
ibogaine, LSD, and other psychedelics into his practice, and told him about its
effectiveness as an addiction treatment, Zeff reexamined his old files. Of all the
patients to whom he’d administered ibogaine, only three had had substance
abuse problems. All three had quit their habits after the ibgoaine session.
“Of everything we tried,” Zeff told Lotsof, “ibogaine achieved the most
profound personal transformation of the patient—which after all is the goal and
purpose of psychiatry. When it worked, the therapist was just a bystander.”
In the last thirty years, there have been about twenty reported deaths relating
to ibogaine, but most of them appeared to have complicating factors. In many
cases, these deaths resulted from unsafe drug combinations, including opioids; in
others, the cause was a preexisting medical condition—particularly heart disease
—or complications related to substance withdrawal.
Ibogaine does have real risks and must be administered carefully, especially
to drug-addicted individuals. In addition to eliminating opioid withdrawal
symptoms, ibogaine also resets a person’s tolerance. A treatment subject who
relapses after an ibogaine session and ingests the usual amount is likely to
overdose. In a clinical setting, these risks can be reduced by prescreening
subjects for health conditions, such as heart problems, providing proper support
and aftercare, and establishing strict measures to avoid the smuggling of drugs
into the treatment center.
For now, ibogaine remains prohibited in the United States, though
underground and offshore clinics continue to provide ibogaine therapy to well-
connected people. In the near future, it’s likely that both international and black
market ibogaine clinics will continue welcoming streams of people desperate for
a second chance. Perhaps someday, if growing evidence confirms what its
believers have been claiming for decades, this unassuming shrub from the shady
undergrowth of the African rainforest will finally have its day in the sun.
MAD HONEY
DISCOVERED DURATION
Known since ancient times; first recorded use in from several hours to several days
401 BCE
ASSOCIATED WITH the nectar of toxic species of rhododendrons, azaleas, and mountain laurel HARVESTED
IN Turkey and Nepal
FIG. 4.6
APIS DORSATA LABORIOSA, OR HIMALAYAN GIANT HONEYBEE
[ ORIGINS AND BACKGROUND ]
ROBABLY THE LAST THING YOU EXPECT when savoring a spoonful of honey is
P to wind up in the hospital with dizziness, tingling extremities, and an altered
state of mind. But if that golden syrup is “mad honey”—or deli bal in
Turkish—that’s a very real risk and, for its connoisseurs, the whole point of
consuming it. Mad honey is produced only in regions where particular species of
rhododendron, azalea, and mountain laurel grow rampant, especially in the
Himalayan cliffs of central Asia and along the southern shores of the Black Sea
in Turkey. These species contain grayanotoxins, a group of poisonous chemicals
that affect the central nervous system.
With a history as both biological weapon and prized inebriant, the honey’s
“mad” moniker is well earned. The nectar’s toxins have no effect on bees, but,
for humans, the resulting honey is incredibly potent.
[ THE EXPERIENCE ]
One spoonful of mad honey is enough to cause noticeable mental and bodily
effects, including a mental high, sensations of movement, and spatial
disorientation. Higher doses lead to convulsions, hallucinations, vomiting, and
problems with breathing and circulation.
Honey intoxication causes a handful of hospital visits every year and in very
rare instances can be fatal. In small amounts, however, the honey is relatively
safe, and for centuries people have enjoyed the subtle changes in consciousness
it provides. Clearly, this is one sweet that demands moderation.
Many Turks consider the honey a medicine, consuming it to treat diabetes, high blood pressure,
and sexual dysfunction.
2-C Family
Boal M. “The Agony & the Ecstasy of Alexander Shulgin.” Playboy. 2004.
Benson T. “All ‘Smiles’: the history of the 2C designer drug class.” The Verge.
www.theverge.com/2015/7/15/8962743/all-smiles-the-history-of-the-2c-designer-drug-class. Published July
15, 2015.
Brown Ethan. “Professor X.” Wired Magazine. September 1, 2002. www.wired.com/2002/09/professorx/.
Published September 1, 2002.
Cohen D. Freud on Coke. Luton, UK: Andrews UK Ltd; 2011.
Mahavishnu. “Between Nothingness and Infinity: An Experience with 2C-B, 2C-C, 2C-E & 2C-I
(exp85144)”. Erowid.org. Jul 22, 2010. www.erowid.org/exp/85144.
Shulgin A. “2,5-dimethoxy-4-bromophenethylamine (2C-B).” Ask Dr. Shulgin Online. Center for Cognitive
Liberty & Ethics. www.cognitiveliberty.org/shulgin/adsarchive/2cb.htm. Published Feb. 7, 2003.
5-MeO-DMT
Wade D, Weil AT. “Identity of a New World Psychoactive Toad.” Ancient Mesoamerica. 1992;3(01):51–59.
doi:10.1017/S0956536100002297.
Weil AT, Davis W. “Bufo alvarius: a potent hallucinogen of animal origin.” J Ethnopharmacol. 1994;41(1-
2):1–8. doi: 10.1016/0378-8741(94)90051-5.
Davis W. “Cultures at the far edge of the world.” TED Talks. YouTube. https://youtu.be/bL7vK0pOvKI.
Grof S. When the Impossible Happens: Adventures in Non-Ordinary Realities. Boulder, CO: Sounds True;
2006.
Amanita muscaria
Feeney K. “Revisiting Wasson’s Soma: exploring the effects of preparation on the chemistry of Amanita
muscaria.” J Psychoactive Drugs. 2010;42(4):499–506.
Feeney K. “The Significance of Pharmacological and Biological Indicators in Identifying Historical uses of
Amanita muscaria.” In: Rush J, ed. Entheogens and the Development of Culture: The Anthropology and
Neurobiology of Ecstatic Experience. Berkeley, CA: North Atlantic Books; 2013:279–318.
Rogers R. The Fungal Pharmacy: The Complete Guide to Medicinal Mushrooms and Lichens of North
America. Berkeley, CA: North Atlantic Books; 2011.
Riedlinger TJ. “Fly-Agaric Motifs in the Cú Chulaind Myth Cycle”. Lecture given at the Mycomedia
Millennium Conference as published on Erowid.org. Oct 29 1999, published by Erowid June 2005.
Miller RJ. Drugged: The Science and Culture Behind Psychotropic Drugs. New York, NY: Oxford
University Press; 2014.
von Bibra BE, Ott J. Plant Intoxicants: A Classic Text on the Use of Mind-Altering Plants. Rochester, VT:
Healing Arts Press; 1995.
von Strahlenberg PJ. An Historico-geographical Description of the North and Eastern Parts of Europe and
Asia; But More Particularly of Russia, Siberia, and Great Tartary. London, England: J. Brotherton; 1738.
Ayahuasca
Levy A. “The Drug of Choice for the Age of Kale.” The New Yorker. Sept. 12, 2016,
www.newyorker.com/magazine/2016/09/12/the-ayahuasca-boom-in-the-u-s.
Metzner R. Sacred Vine of Spirits: Ayahuasca. Rochester, VT: Inner Traditions • Bear & Co; 2005.
Sanches RF, et al. “Antidepressant Effects of a Single Dose of Ayahuasca in Patients With Recurrent
Depression: A SPECT Study.” J Clin Psychopharmacol. 2016;36(1):77–81. doi:
10.1097/JCP.0000000000000436.
Halpern JH, et al. “Evidence of health and safety in American members of a religion who use a
hallucinogenic sacrament.” Med Sci Monit. 2008;14(8):SR15–22.
Grob CS, et al. “Human psychopharmacology of hoasca, a plant hallucinogen used in ritual context in
Brazil.” J Nerv Ment Dis. 1996;184(2):86–94.
Frecska E, et al. “The Therapeutic Potentials of Ayahuasca: Possible Effects against Various Diseases of
Civilization.” Front Pharmacol. 2016;7:35. doi: 10.3389/fphar.2016.00035.
Kandell J, Richard E. “Schultes, 86, Dies; Trailblazing Authority on Hallucinogenic Plants.” The New York
Times. Apr. 13, 2001, www.nytimes.com/2001/04/13/us/richard-e-schultes-86-dies-trailblazing-authority-
on-hallucinogenic-plants.html.
Rudgley R. The Encyclopedia of Psychoactive Substances. London, England: Little, Brown & Company;
1998:26.
Cannabis
Abel EL. “Cannabis in the Ancient World.” Marihuana: the first twelve thousand years. New York, NY:
Plenum Publishing; 1980.
Russo EB, et al. “Phytochemical and genetic analyses of ancient cannabis from Central Asia.” J Exp Bot.
2008;59(15)4171–4182. doi: 10.1093/jxb/ern260.
Clarke R, Merlin M. Cannabis: Evolution and Ethnobotany. Oakland, CA: University of California Press;
2013.
Rätsch C. Marijuana Medicine: A World Tour of the Healing and Visionary Powers of Cannabis. Rochester,
VT: Healing Arts Press; 2001.
Walton RP. “Description of the Hashish Experience.” In: Marihuana: America’s New Drug Problem.
Philadelphia, Pennsylvania: J. B. Lippincott; 1938:86–114. www.cannabiscure.info/wp-
content/uploads/2016/07/Description-of-the-Hashish-Experience-R.-P.-Walton-M.D.-1938.pdf.
Brown DT. Cannabis: The Genus Cannabis. UK: Harwood Academic Publishers; 1998.
Shi Y. “Medical marijuana policies and hospitalizations related to marijuana and opioid pain reliever.” Drug
Alcohol Depend. 2017;173:144–150. doi: https://doi.org/10.1016/j.drugalcdep. 2017.01.006.
DiPT
Blom JD, Sommer IEC. Hallucinations: Research and Practice. New York, NY: Springer Publishing; 2012.
Shulgin AT, Carter MF. “N, N-Diisopropyltryptamine (DIPT) and 5-methoxy-N,N-diisopropyltryptamine
(5-MeO-DIPT). Two orally active tryptamine analogs with CNS activity.” Commun Psychopharmacol.
1980;4(5):363–9.
Acrimonius Funk. “Not Unlike a Velvety, Saucey, French Dish: An Experience with DiPT & Salvia
divinorum (20x extract) (exp56700).” Erowid.org. Oct 19, 2006. www.erowid.org/exp/56700.
Kaleida. “Long Lost Novelty Restored: An Experience with DiPT (exp107477).” Erowid.org. Feb 23, 2016.
www.erowid.org/exp/107477.
Azureskies. “An Economical Auditory Adventure: An Experience with DiPT (exp19709).” Erowid.org.
Mar 15, 2007. www.erowid.org/exp/19709.
Anonymous. “Music Was Broken: An Experience with DiPT (exp14610).” Erowid.org. May 12, 2002.
www.erowid.org/exp/14610.
Corey V, et al. “Psychoactive Substances.” In: Blom JD, Sommer IEC, eds. Hallucinations: Research and
Practice. New York, NY: Springer;2012:297–316.
DMT
Strassman R. DMT: The Spirit Molecule, A Doctor’s Revolutionary Research into the Biology of Near-
Death and Mystical Experiences. Rochester, VT: Park Street Press; 2000.
Szara S. “The Comparison of the Psychotic Effect of Tryptamine Derivatives with the Effects of Mescaline
and LSD-25 in Self-Experiments.” In: Garattini S, Ghetti V, eds. Psychotropic Drugs. New York, NY:
Elsevier; 1957:460.
Leary T. High Priest. Berkeley, CA: Ronin Publishing; 1995:215 and 267.
McKenna TK, McKenna DJ. The Invisible Landscape: Mind, Hallucinogens, and the I Ching. San
Francisco, CA: HarperCollins; 1993.
McKenna TK. “Nature Is the Center of the Mandala.” Presented at: Shared Visions Bookstore, Berkeley,
California, September 12, 1987. YouTube. https://youtu.be/5DfW_1gj8Zk.
McKenna TK. “Rap Dancing into the 3rd Millennium.” Presented at: Starwood XIV Festival, Brushwood
Folklore Center, Sherman, New York, July 19–24, 1994. YouTube. https://youtu.be/gMUqaFwmhG0.
McKenna TK, with Zuvuya. “Dream Matrix Telemetry.” Dream Matrix Telemetry, Delirium Records, 1993.
Szára S. “DMT at fifty.” Neuropsychopharmacol Hung. 2007;9(4):201–5.
DOx
Parker SF. Conversations with Ken Kesey. Jackson, MS: University Press of Mississippi; 2014.
Bureau of Drug Abuse Control. Micro-Gram. Nov 1967;1(1):1–2.
www.erowid.org/library/periodicals/microgram/microgram_1967_11_v01n01.pdf.
Bureau of Narcotics and Dangerous Drugs. Microgram. May 1968;1(8):2.
www.erowid.org/library/periodicals/microgram/microgram_1968_04_v01n07.pdf.
Yu B, et al. “Serotonin 5-Hydroxytryptamine2A Receptor Activation Suppresses Tumor Necrosis Factor- α-
Induced Inflammation with Extraordinary Potency.” J Pharmacol Exp Ther. 2008;327(2):316–323.
doi:10.1124/jpet.108.143461.
Gabelt BT, et al. “Aqueous Humor Dynamics in Monkeys after Topical R-DOI.” Invest Ophthalmol Vis Sci.
2005;46(12):4691–6. doi: 10.1167/iovs.05-0647.
Morris H, Smith A. “The Last Interview with Alexander Shulgin.” VICE. May 1, 2010.
www.vice.com/en_se/article/the-last-interview-with-alexander-shulgin-423-v17n5. Published May 1, 2010.
Dawks. “Is DOx any good?” Shroomery. July 4, 2013.
www.shroomery.org/forums/showflat.php/Number/18555338. Published July 4, 2013.
Barfknecht CF, Nichols DE. “Potential psychotomimetics. Bromomethoxyamphetamines.” J. Med. Chem.
1971 Apr;14(4)370–372.
Shulgin AT, et al. “4-Bromo-2,5-Dimethoxyphenylisopropylamine, a new centrally active amphetamine
analog.” Pharmacology. 1971;5(2)103–107.
DXM
Stanciu CN, et al. “Recreational use of dextromethorphan, ‘Robotripping’–A brief review.” Am J Addict.
2016 Aug;25(5):374–7. doi: 10.1111/ajad.12389.
Morris H, Wallach J. “From PCP to MXE: a comprehensive review of the non-medical use of dissociative
drugs.” Drug Test Anal. 2014 Jul–Aug;6(7-8):614–32. doi: 10.1002/dta.1620.
Anonymous. “My First Trip: An Experience with DXM (exp1883).” Erowid.org. Jun 16, 2000.
www.erowid.org/exp/1883.
Addy P. “Facilitating Transpersonal Experiences with Dextromethorphan: Potential, Cautions, and
Caveats.” Journal of Transpersonal Psychology. 2007;39(1):1–22.
J Gelfer. “Towards a Sacramental Understanding of Dextromethorphan.” J Alt Spirit New Age Stud. 2007
Sep;3:80–96.
DeRogatis J. “Let It Blurt, The Life and Times of Lester Bangs, America’s Greatest Rock Critic.” New
York, NY: Broadway Books; 2000:37–38.
The Shadow. “DXM, a double-edged sword: An Experience with DXM (exp72).” Erowid.org. Oct 13,
2000. www.erowid.org/exp/72.
Thgilenin. “Beyond Words: An Experience with DXM (exp180).” Erowid.org. Aug 15, 2001.
www.erowid.org/exp/180.
Xerxes. “Weird Memories On This Nervous Night: An Experience with DXM (exp6511).” Erowid.org. Feb
28, 2002. www.erowid.org/exp/6511.
White W. “The Dextromethorphan FAQ: Answers to Frequently Asked Questions about DXM.”
Erowid.org. www.erowid.org/chemicals/dxm/faq/dxx_faq.shtml.
Iboga
Ravalec V, et al. Iboga: The Visionary Root of African Shamanism. Rochester, VT: Park Street Press; 2004.
Lotsof HS. “Ibogaine in the treatment of chemical dependence disorders: clinical perspectives.” Bull.
MAPS. 1995;5:16–27.
Brown TK. “The use of ibogaine in the treatment of substance dependence.” Current Drug Abuse Reviews.
2013;6(1):3–13. doi: 10.2174/15672050113109990001.
Smyth BP, et al. “Lapse and relapse following inpatient treatment of opiate dependence.” Ir Med J.
2010;103(6):176–9.
Cappendijk SLT, Dzoljic MR. “Inhibitory effects of ibogaine on cocaine self-administration in rats.” Eur J
Pharmacol. 1993;241(2–3):261–5. https://doi.org/10.1016/0014-2999(93)90212-Z.
Rezvani AH, et al. “Attenuation of alcohol intake by ibogaine in three strains of alcohol-preferring rats.”
Pharmacol Biochem Behav. 1995;52(3):615–20. doi: 10.1016/0091-3057(95)00152-M.
Alper KR, et al. “Fatalities temporally associated with the ingestion of ibogaine.”J Forensic Sci.
2012;57(2):398–412. doi: 10.1111/j.1556-4029.2011.02008.x.
Alper KR, et al. “The ibogaine medical subculture.” J Ethnopharmacol. 2008;115(1):9–24. doi:
10.1016/j.jep.2007.08.034.
Alper KR, et al. “A Contemporary History of Ibogaine in the United States and Europe.” The Alkaloids
Chemistry and Biology. 2001;56:249–81.
Freedlander J. “Ibogaine: A Novel Anti-Addictive Compound—A Comprehensive Literature Review.”
Journal of Drug Education and Awareness. 2003;1:79–98.
Mutual_Ascendency. “Me and The Loon: An Experience with Tabernathe Iboga (Rootbark) (exp103942).”
Erowid.org. Jan 2, 2016. www.erowid.org/exp/103942.
Ketamine
Garcia-Romeu A, et al. “Clinical applications of hallucinogens: A review.” Exp Clin Psychopharmacol.
2016;24(4):229–268. doi: 10.1037/pha0000084.
Jansen K. Ketamine: dreams and realities. Sarasota, FL: Multidisciplinary Association for Psychedelic
Studies; 2001.
Domino EF. “Taming the Ketamine Tiger.” Anesthesiology. 2010;113:678–684.
https://doi.org/10.1097/aln.0b013e3181ed09a2.
Hooper J. “John Lilly: Altered States.” Omni Magazine. Jan 1983.
Morgan CJA, Curran HV. “Ketamine use: a review.” Addiction. 2012;107(1):27–38.
https://doi.org/10.1111/j.1360-0443.2011.03576.x.
Muetzelfeldt L, et al. “Journey through the K-hole: phenomenological aspects of ketamine use.” Drug
Alcohol Depend. 2008;95(3):219–29.
Krupitsky EM, Grinenko AY. “Ketamine Psychedelic Therapy (KPT): A Review of the Results of Ten Years
of Research.” Journal of Psychoactive Drugs. 1997;29:165–183.
https://doi.org/10.1080/02791072.1997.10400185.
Niesters M, et al A. “Ketamine for chronic pain: risks and benefits.” Br J Clin Pharmacol. 2014;77(2):357–
67. doi: 10.1111/bcp.12094.
LSD
Lee MA, Shlain B. Acid Dreams, the Complete Social History of LSD: the CIA, the Sixties, and Beyond.
New York, NY: Grove Press; 1985.
Sewell RA, et al. “Response of cluster headache to psilocybin and LSD.” Neurology. 2006;66(12):1920–2.
doi: https://doi.org/10.1212/01.wln.0000219760.05466.43.
Carhart-Harris RL, et al. “Neural correlates of the LSD experience revealed by multimodal neuroimaging.”
Proc Natl Acad Sci USA. 2016;113(17):4853–8. doi:10.1073/pnas.1518377113.
Gasser P, et al. “Safety and efficacy of LSD-assisted psychotherapy for anxiety associated with life-
threatening diseases.” J Nerv Ment Dis. 2014;202(7):513–520. doi: 10.1097/NMD.0000000000000113.
Gasser P, et al. “LSD-assisted psychotherapy for anxiety associated with a life-threatening disease: a
qualitative study of acute and sustained subjective effects.” J Psychopharmacol. 2015;29(1):57–68.
https://doi.org/10.1177/0269881114555249.
Grof S, et al. “LSD-assisted psychotherapy in patients with terminal cancer.” Int Pharmacopsychiatry.
1973;8(3):129–144.
Jay Stevens. Storming Heaven: LSD and the American Dream. New York, NY: Grove Press; 1998: 208.
Krebs TS, Johansen PØ. “Lysergic acid diethylamide (LSD) for alcoholism: meta-analysis of randomized
controlled trials.” J Psychopharmacol. 2012;26(7):994–1002. doi: 10.1177/0269881112439253.
Dolder PC, et al. “LSD Acutely Impairs Fear Recognition and Enhances Emotional Empathy and Sociality.”
Neuropsychopharmacology. 2016 Oct;41(11):2638–2646. doi:10.1038/npp.2016.82.
Kaelen M, et al. “LSD enhances the emotional response to music.” Psychopharmacology.
2015;232(19):3607–14. https://doi.org/10.1007/s00213-015-4014-y.
Hartogsohn I. “The American Trip: Set, Setting, and Psychedelics in 20th Century Psychology.” Bull.
MAPS. 2013;23(1):6–9.
Hofmann A. LSD—My Problem Child. Santa Cruz, CA: MAPS; 2009.
Wold R. “LSD and Psilocybin for Cluster Headaches: Preventing Pain, Saving Lives.” Bull. MAPS.
2013;Special Edition:34–35.
Mad Honey
Williams C. Medicinal Plants in Australia Volume 1: Bush Pharmacy. Kenthurst, NSW: Rosenberg
Publishing; 2010:223.
Lensky Y. Bee Products: Properties, Applications, and Apitherapy. Boston, MA: Springer; 1997.
Mayor A. “Mad Honey!” Archaeology. 1995;48(6):32–40.
Rätsch C. Encyclopedia of Psychoactive Plants: Endopharmacology and Its Applications. South Paris, ME:
Park Street Press; 2005: 751–4.
Ott J. “The Delphic bee: Bees and toxic honeys as pointers to psychoactive and other medicinal plants.”
Economic Botany. 1998;52(3):260–266. https://doi.org/10.1007/BF02862143.
Caprara D. “Hunting for Hallucinogenic Honey in Nepal.” VICE. September 13, 2016.
www.vice.com/en_uk/article/hunting-for-hallucinogenic-honey-in-nepal-v23n6. Published September 13,
2016.
MDA
Mannich C, et al. “Über Oxyphenyl-alkylamine und Dioxyphenyl-alkylamine.” Ber Dtsc. Chem Ges.
1910;43:189–197. doi:10.1002/cber.19100430126.
Baggott MJ, et al. “Investigating the Mechanisms of Hallucinogen-Induced Visions Using 3,4-
Methylenedioxyamphetamine (MDA): A Randomized Controlled Trial in Humans.” PLoS ONE.
2010;5(12):e14074. https://doi.org/10.1371/journal.pone.0014074.
Naranjo C, et al. “Evaluation of 3,4-Methylenedioxyamphetamine (MDA) as an adjunct to psychotherapy.”
Med Pharmacol Exp Int J Exp Med. 1967;17(4):359–64.
Stolaroff MJ. The Secret Chief Revealed, Conversations with Leo Zeff, Pioneer in the Underground
Psychedelic Psychotherapy Movement. Santa Cruz, CA: MAPS; 2004.
Turek IS, et al. “Methylendedioxyamphetamine (MDA) subjective effects.” J Psychedelic Drugs.
1974;6(1):7–14.
Weil AT. “The Love Drug.” J of Psychedelic Drugs. 1976 Oct–Dec;8(4):335–337.
Associated Press. “$700,000 Awarded to Estate of Army Drug Test Victim.” May 6, 1987. Los Angeles
Times. http://articles.latimes.com/1987-05-06/news/mn-2486_1_chemical-warfare-agents. Published May 6,
1987.
Zinberg N. “Observations on the Phenomenology of Consciousness Change.” J of Psychedelic Drugs.
1976;8(1):59–76.
MDMA
Substance Abuse and Mental Health Services Administration. Results from the 2013 National Survey on
Drug Use and Health: Summary of National Findings, NSDUH Series H-48, HHS Publication No. (SMA)
14-4863. Rockville, MD: Substance Abuse and Mental Health Services Administration; 2014. Table 1.1B.
Nelson RJ. An Introduction to Behavioral Endocrinology. 3rd Ed. Sunderland, MA: Sinauer Associates;
2005:669–720.
Gasser P. “Psycholytic therapy with MDMA and LSD in Switzerland.” Newsletter of the Multidisciplinary
Association for Psychedelic Studies. 1994–5;5(3):3–7.
Johansen PØ, Krebs TS. “Psychedelics not linked to mental health problems or suicidal behavior: a
population study.” J Psychopharmacol. 2015;29(3):270–9. https://doi.org/10.1177/0269881114568039.
Greer G, Tolbert R. “Subjective Reports of the Effects of MDMA in a Clinical Setting.” J of Psychoactive
Drugs. 1986;18(4):319–327. https://doi.org/10.1080/02791072.1986.10472364.
Garcia-Romeu A, et al. “Clinical applications of hallucinogens: A review.” Exp Clin Psychopharmacol.
2016;24(4)229–268. https://doi.org/10.1037/pha0000084.
Doblin R, Rosenbaum, M. “Why MDMA Should Not Have Been Made Illegal.” In: Inciardi JA, ed. The
Drug Legalization Debate (2nd Ed.). London, England: Sage Publications, Inc.;1991.
Beck J, Rosenbaum M. “The Distribution of Ecstasy.” In: Pursuit of Ecstasy: The MDMA Experience.
Albany, NY: State University of New York Press; 1994.
St. John G. Rave Culture and Religion. London, England: Routledge; 2004:149.
Macie T. “I’m a veteran who overcame treatment-resistant PTSD after participating in a clinical study of
MDMA-assisted psychotherapy. My name is Tony Macie—Ask me anything!” Reddit. April 16, 2014.
www.reddit.com/r/IAmA/comments/236o6g/im_a_veteran_who_overcame_treatmentresistant_ptsd/.
Published April 16, 2014.
Freudenmann R W, et al. “The origin of MDMA (ecstasy) revisited: the true story reconstructed from the
original documents.” Addiction. 2006;101(9):1241–1245. https://doi.org/10.1111/j.1360-
0443.2006.01511.x.
Morning Glory
Carod-Artal FJ. “Hallucinogenic drugs in pre-Columbian Mesoamerican cultures.” Neurologia.
2015;30(1):42–9. https://doi.org/10.1016/j.nrleng.2011.07.010.
Niño-Maldonado AI, et al. “Efficacy and tolerability of intravenous methylergonovine in migraine female
patients attending the emergency department: a pilot open-label study.” Head Face Med. 2009;5:21.
https://doi.org/10.1186/1746-160X-5-21.
Ott J. “The Delphic bee: Bees and toxic honeys as pointers to psychoactive and other medicinal plants.”
Economic Botany. 1998;52(3):260–266.
Koehler PJ, Tfelt-Hansen PC. “History of methysergide in migraine.” Cephalalgia. 2008;28(11):1126–35.
https://doi.org/10.1111/j.1468-2982.2008.01648.x.
Durán D. Historia de las Indias de Nueva Espãna. México: Editorial Porrúa; 1967.
Stafford PG, Bigwood J. Psychedelics Encyclopedia. Berkeley, CA: Ronin Publishing; 1992:118–9.
Nitrous Oxide
Austin JH. Zen and the Brain: Toward an Understanding of Meditation and Consciousness. Cambridge
MA: MIT Press; 2015:407–410.
Brown DJ. The New Science of Psychedelics: At the Nexus of Culture, Consciousness, and Spirituality.
Rochester, VT: Park Street Press; 2013.
Gillman MA, Lichtigfeld FJ. “Analgesic nitrous oxide for alcohol withdrawal: a critical appraisal after 10
years’ use.” Postgrad Med J. 1990;66(777):543–6.
Gillman MA, Lichtigfeld FJ. “Enlarged double-blind randomised trial of benzodiazepines against
psychotropic analgesic nitrous oxide for alcohol withdrawal.” Addict Behav. 2004;29(6):1183–7.
Jacobsohn PH. “Horace Wells: discoverer of anesthesia.” Anesth Progr. 1995;42(3–4):73–75.
James W. “Subjective Effects of Nitrous Oxide.” Mind. 1882; Vol 7.
Nagele P, et al. “Nitrous oxide for treatment-resistant major depression: A proof-of-concept trial.” Biol
Psychiatry. 2015;78(1):10–18. http://dx.doi.org/10.1016/j.biopsych.2014.11.016.
Ojutkangas R, Gillman MA. “Psychotropic analgesic nitrous oxide for treating alcohol withdrawal in an
outpatient setting.” Int J Neurosci. 1994;76(1–2):35–9.
Tymoczko D. “The Nitrous Oxide Philosopher.” The Atlantic Monthly. 1996 May;277(5):93–101.
www.theatlantic.com/magazine/archive/1996/05/the-nitrous-oxide-philosopher/376581/.
Austin JH. Zen and the Brain: Toward an Understanding of Meditation and Consciousness. Cambridge
MA: MIT Press; 2015:407–410.
Peyote
Huffman B. “Ken Kesey.” The Literary Encyclopedia. First published 17 May 2002.
www.litencyc.com/php/speople.php?rec=true&UID=4941.
Terry M, et al. “Lower Pecos and Coahuila Peyote: New Radiocarbon Dates.” Journal of Archaeological
Science. 2006;33(7):1017–1021. https://doi.org/10.1016/j.jas.2005.11.008.
Boyd CE. The Rock Art of the Lower Pecos. College Station, TX: Texas A & M University Press; 2003.
Boyd CE, Dering JP. “Medicinal and Hallucinogenic Plants Identified in the Sediments and the Pictographs
of the Lower Pecos, Texas Archaic.” Antiquity. 1996;70(268):256–275. doi: 10.1017/S0003598X00083265.
Stewart OC. Peyote Religion. Norman, OK: University of Oklahoma Press; 1987:24–42.
Huxley A. The Doors of Perception. UK: Chatto & Windus; 1954.
Gottlieb A. Peyote and Other Psychoactive Cacti. Berkeley, CA: Ronin Publishing; 1997.
Halpern JH, et al. “Psychological and Cognitive Effects of Long-Term Peyote Use Among Native
Americans.” Biological Psychiatry. 2005;58(8):624–631. https://doi.org/10.1016/j.biopsych.2005.06.038.
Psilocybin
Griffiths RR, et al. “Mystical- type experiences occasioned by psilocybin mediate the attribution of personal
meaning and spiritual significance 14 months later.” J Psychopharmacol. 2008;22(6):620–632.
https://doi.org/10.1177/0269881108094300.
Lattin D. The Harvard Psychedelic Club: How Timothy Leary, Ram Dass, Huston Smith, and Andrew Weil
Killed the Fifties and Ushered in a New Age for America. New York, NY: Harper Collins; 2011.
Doblin R. “Dr. Leary’s Concord Prison Experiment: A 34-Year Follow-up Study.” J Psychoactive Drugs.
1998;30(4):419–26. https://doi.org/10.1080/02791072.1998.10399715.
Kingsborough, Lord. Antiquities of Mexico. (Ritos antiquos, vol. 9). London and New York;1848:17.
Samorini G. “The Oldest Representations of Hallucinogenic Mushrooms in the World (Sahara Desert,
9000–7000 B.P.).” INTEGRATION Journal of Mind-moving Plants and Culture, 1992;2&3:69–78.
Schleiffer H. Sacred Narcotic Plants of the New World Indians. New York, NY: Hafner Press; 1973:20–21.
Grob CS, et al. “Pilot study of psilocybin treatment for anxiety in patients with advanced-stage cancer.”
Arch Gen Psychiatry. 2011 Jan;68(1):71–8. doi: 10.1001/archgenpsychiatry.2010.116.
Moreno FA, et al. “Safety, tolerability, and efficacy of psilocybin in 9 patients with obsessive-compulsive
disorder.” J Clin Psychiatry. 2006;67(11):1735–40.
Cowen P. “Altered states: psilocybin for treatment-resistant depression.” The Lancet Psychiatry.
2016;3(7):592–3. https://doi.org/10.1016/s2215-0366(16)30087-6.
Carhart-Harris RL, et al. “Psilocybin with psychological support for treatment-resistant depression: an
open-label feasibility study.” The Lancet Psychiatry. 2016;3(7):619–627. https://doi.org/10.1016/s2215-
0366(16)30065-7.
Lebedev AV, et al. “Finding the self by losing the self: Neural correlates of ego-dissolution under
psilocybin.” Human Brain Mapping. 2015;36(6):2027–2038. https://doi.org/10.1002/hbm.22833.
Hendricks PS, et al. “Psilocybin, psychological distress, and suicidality.” J Psychopharmacol. 2015
Sep;29(9):1041–1043. https://doi.org/10.1177/0269881115598338.
Hendricks PS, et al. “The relationships of classic psychedelic use with criminal behavior in the United
States adult population.” J Psychopharmacol. 2017;32(1):37–48.
https://doi.org/10.1177/0269881117735685.
Schultes RE, Hofmann A, Plants of the Gods: Their Sacred, Healing, and Hallucinogenic Powers.
Rochester, VT: Healing Arts Press; 1992:149.
Salvia
Valdés LJ III. The Early History of Salvia divinorum. The Entheogen Review. 2001;10(3):73–75.
Epling C, Játiva-M C. “A new species of Salvia from Mexico.” Botanical Museum Leaflets, Harvard
University. 1962;20(3):75–76.
Valdés LJ III, et al. “Ethnopharmacology of Ska María Pastora (Salvia Divinorum, Epling and Játiva-M.).”
J. Ethnopharmacology. 1983;7:287–312.
Johnson JB. “The elements of Mazatec witchcraft.” Etnologiska Studier. 1939;9:128–150.
Roth BL, et al. “Salvinorin A: A potent naturally occurring nonnitrogenous kappa opioid selective agonist.”
Proc Natl Acad Sci U S A. 2002;99(18):11934–9.
Ortega A, et al. “Salvinorin, a new trans-neoclerodane diterpene from Salvia divinorum (Labiatae).”
Journal of the Chemical Society Perkins Transactions 1. 1982;0:2505–8.
San Pedro
Yerman D. The Great Cacti: Ethnobotany & Biogeography. Tuscon, AZ: University of Arizona Press;
2007:220–224.
Anderson EF. The Cactus Family. Portland, OR: Timber Press; 2001:45–49.
Hayes C. Tripping: An Anthology of True-life Psychedelic Adventures. Canada: Penguin Compass;
2001:328–331.
Davis EW. Sacred Plants of the San Pedro Cult. Botanical Museum Leaflets, Harvard University,
1983;29(4):367–386
Bussmann RW, Sharon D. “Traditional medicinal plant use in Northern Peru: tracking two thousand years
of healing culture.” J Ethnobiol Ethnomed. 2006;2:47.
Yopo
Kärkkäinen J, et al. “Urinary excretion of free bufotenin by psychiatric patients.” Biol Psychiatry.
1988;24(4):44I–446. https://doi.org/10.1016/0006-3223(88)90182-5.
Ott J. Pharmacotheon:Entheogenic Drugs, Their Plant Sources and History. Kennewick, WA: Natural
Products Company; 1993:164–5.
Stafford PG, Bigwood J. Psychedelics Encyclopedia. Berkeley, CA: Ronin Publishing; 1992:309-331.
de Smet PAGM. “A multidisciplinary overview of intoxicating enema rituals in the western hemisphere.” J
Eihnophormacol 1983 Dec;9(2–3):129–66.
Altschul S. “The genus Anadenanthera in Amerindian cultures.” Cambridge, MA: Botanical Museum,
Harvard University; 1972.
Safford WE. “Identity of Cohoba, the Narcotic Snuff of Ancient Haiti.” Journal of the Washington Academy
of Sciences. 1916;6:547–562.
Emanuele E, et al. “Elevated urine levels of bufotenine in patients with autistic spectrum disorders and
schizophrenia.” Neuro Endocrinol Lett. 2010;31(1):117–1.
[ INDEX ]
2C family
experience, 24
origins, 21
research, 22
therapy, 27
variations, 22, 26
5-Bromo-DMT, 203, 207
5-MeO-DMT
epená powder, 31
experience, 31
human source of, 30
origins, 29
potency, 32
yopo and, 112
cannabis
experience, 188
forms of, 186
hash oil, 187
hemp uses, 188
hybrid strains, 186
indica strains, 186
origins, 185
Rastafari movement, 190
safety, 185, 192
sativa strains, 186
spirituality and, 189, 190
therapy, 191
tinctures, 188
Cárdenas, Juan de, 77
Carhart-Harris, Robin, 71, 72, 97, 98, 99
Carter, Michael, 21
changa, 46
Churchill, Winston, 158
cohoba, 111
Coleridge, Samuel, 161
Columbus, Christopher, 111
Concord Prison Experiment, 95
Cooper, Philip, 106
Davis, Wade, 31
Davy, Sir Humphry, 158, 160
default mode network (DMN), 71
Dionysian Mysteries, 220
DiPT
auditory distortions, 195, 196
experience, 195, 196, 199
origins, 195
research, 200
safety, 198
DMT
changa blends, 46
experience, 45, 47, 48, 51
human source of, 45, 46
origins, 45
research, 47, 50
yopo and, 112
DMT: The Spirit Molecule (Rick Strassman), 51
Doblin, Rick, 10, 132
Domino, Edward, 150
Domino, Toni, 150
The Doors of Perception (Aldous Huxley), 86, 87
DOx family
DOI, 58
DOM, 55, 56, 57
origins, 55
research, 56, 57
variations, 55, 58, 59
DXM
empathogenic effects, 140
experience, 139, 143
lower plateaus, 139
origins, 137
research, 144
therapy, 138, 140, 144
upper plateaus, 141
fish intoxication
experience, 205
goatfish, 204
indigenous use, 203, 205
origins, 203
rabbitfish, 204
research, 208
safety, 205
salema porgy, 204
sea bream, 204, 206
fly agaric. See Amanita muscaria.
Fung, Rosa, 104
iboga
experience, 213
indigenous use, 212
origins, 211
research, 216
therapy, 215
Kamchatka, 180
Kerouac, Jack, 138
Kesey, Ken, 57, 68
ketamine
dissociation, 150
experience, 149, 150
origins, 147
rave scene, 152
research, 148, 151
safety, 147, 152, 153
therapy, 148, 154
Kopec, Joseph, 179
Krupitsky, Evgeny, 154
Leary, Timothy, 39, 47, 56, 67, 69, 93, 94, 95, 96, 100
Lilly, John C., 151
Lotsof, Howard, 215, 216
LSD
experience, 63, 64, 65
forms of, 62
microdosing, 70
origins, 61
research, 62, 63, 70
safety, 64, 66, 69
therapy, 61, 65, 68, 70, 71, 72
Ram Dass, 57
Rätsch, Christian, 106
Reko, Blas Pablo, 92
Rig Veda, 181
Robbins, Tom, 182
Roberts, Joe, 206
Roget, Peter Mark, 161
TiHKAL (Tryptamines I Have Known and Loved) (Alexander and Ann Shulgin), 24, 196
trip reports, 10
vilca beans
bufotenine, 112
cohoba, 111
experience, 111
indigenous use, 109, 110, 111
origins, 109
research, 112
therapy, 113
Xenophon, 220
yopo
bufotenine, 112
cohoba, 111
experience, 111
indigenous use, 109, 110, 111
origins, 109
research, 112
therapy, 113
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