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Preference for Palatable Food, Impulsivity, and Relation to Drug Addiction in Rats

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Animal Models of Eating Disorders

Part of the book series: Neuromethods ((NM,volume 161))

Abstract

Overall, this review focuses mainly on the behavioral overlap and interaction between drug abuse and excessive behavior directed toward natural rewards. In recent years, rats selectively bred for high (HiS) or low (LoS) saccharin intake and tested for all phases of drug addiction have provided valuable information regarding vulnerability to drug (Carroll et al., Behav Pharmacol 19:435–60, 2008) and food (Avena, Appetite 55:734–7, 2010; Yakovenko et al., Appetite 57:397–400, 2011) dependence/addiction, related affective disorders, and impulsive behavior. The neurobiological bases for this interaction between drug and food rewards have been reviewed by others (Deadwyler, Ann N Y Acad Sci 1187:140–7, 2010; Volkow and Wise, Nat Neurosci 8:555–60, 2005; Olsen, Neuropharmacology 61:1109–22, 2011). The HiS and LoS rats are models of the heritability of maladaptive behaviors, including hallmarks of drug dependence, bingeing, and withdrawal that serve equally well for the understanding of binge eating. The purpose of this chapter is to review recent developments in this area of research, emphasizing that several commonalities between food and drug addiction have been revealed, and to highlight similar connections between other individual differences and their relationships to sweet preference and drug abuse. Impulsivity will also be discussed as a major marker of addiction vulnerability that covaries with sweet preference, as well as other vulnerability factors, such as age (adolescents vs. adults) and sex. New evidence is presented regarding the importance of reactivity to aversive events in predicting drug abuse in HiS and LoS rats and on the importance of other addiction-prone and addiction-resistant phenotypes. Recent data from animal models also suggest that the addiction-prone and addiction-resistant groups (e.g., HiS, LoS) respond in opposite ways when treated for drug abuse. Finally, new evidence shows the importance of self-initiated and self-maintained treatments to reduce vulnerability to behavioral excesses and incubation of craving after termination of their use.

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References

  1. Carroll ME et al (2008) Selective breeding for differential saccharin intake as an animal model of drug abuse. Behav Pharmacol 19:435–460

    Article  CAS  PubMed  Google Scholar 

  2. Yakovenko V et al (2011) Food dependence in rats selectively bred for low versus high saccharin intake. Implications for “food addiction”. Appetite 57:397–400

    Article  PubMed  Google Scholar 

  3. Deadwyler SA (2010) Electrophysiological correlates of abused drugs: relation to natural rewards. Ann N Y Acad Sci 1187:140–147

    Article  CAS  PubMed  Google Scholar 

  4. Volkow ND, Wise RA (2005) How can drug addiction help us understand obesity? Nat Neurosci 8:555–560

    Article  CAS  PubMed  Google Scholar 

  5. Olsen CM (2011) Natural rewards, neuroplasticity, and non-drug addictions. Neuropharmacology 61:1109–1122

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Goodwin DW et al (1973) Alcohol problems in adoptees raised apart from alcoholic biological parents. Arch Gen Psychiatry 28:238–243

    Article  CAS  PubMed  Google Scholar 

  7. Cadoret RJ et al (1986) An adoption study of genetic and environmental factors in drug abuse. Arch Gen Psychiatry 43:1131–1136

    Article  CAS  PubMed  Google Scholar 

  8. Agrawal A, Lynskey MT (2008) Are there genetic influences on addiction: evidence from family, adoption and twin studies. Addiction 103:1069–1081

    Article  PubMed  Google Scholar 

  9. Bardo MT, Donohew RL, Harrington NG (1996) Psychobiology of novelty seeking and drug seeking behavior. Behav Brain Res 77:23–43

    Article  CAS  PubMed  Google Scholar 

  10. Blanchard MM, Mendelsohn D, Stamp JA (2009) The HR/LR model: further evidence as an animal model of sensation seeking. Neurosci Biobehav Rev 33:1145–1154

    Article  PubMed  Google Scholar 

  11. Piazza PV et al (1989) Factors that predict individual vulnerability to amphetamine self-administration. Science 245:1511–1513

    Article  CAS  PubMed  Google Scholar 

  12. Kabbaj M (2006) Individual differences in vulnerability to drug abuse: the high responders/low responders model. CNS Neurol Disord Drug Targets 5:513–520

    Article  PubMed  Google Scholar 

  13. Deroche-Gamonet V, Belin D, Piazza PV (2004) Evidence for addiction-like behavior in the rat. Science 305:1014–1017

    Article  CAS  PubMed  Google Scholar 

  14. Davis BA et al (2008) The effects of novelty-seeking phenotypes and sex differences on acquisition of cocaine self-administration in selectively bred High-Responder and Low-Responder rats. Pharmacol Biochem Behav 90:331–338

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Howard MO, Kivlahan D, Walker RD (1997) Cloninger’s tridimensional theory of personality and psychopathology: applications to substance use disorders. J Stud Alcohol 58:48–66

    Article  CAS  PubMed  Google Scholar 

  16. Lovallo WR (2006) Cortisol secretion patterns in addiction and addiction risk. Int J Psychophysiol 59:195–202

    Article  PubMed  PubMed Central  Google Scholar 

  17. Iacono WG, Malone SM, McGue M (2008) Behavioral disinhibition and the development of early-onset addiction: common and specific influences. Annu Rev Clin Psychol 4:325–348

    Article  PubMed  Google Scholar 

  18. Mackillop J et al (2011) Delayed reward discounting and addictive behavior: a meta-analysis. Psychopharmacology 216:305–321

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Carroll ME, Anker JJ (2010) Sex differences and ovarian hormones in animal models of drug dependence. Horm Behav 58:44–56

    Article  CAS  PubMed  Google Scholar 

  20. Carroll ME, Anker JJ, Perry JL (2009) Modeling risk factors for nicotine and other drug abuse in the preclinical laboratory. Drug Alcohol Depend 104 Suppl 1:S70–S78

    Article  PubMed  CAS  Google Scholar 

  21. Riley AL (2011) The paradox of drug taking: the role of the aversive effects of drugs. Physiol Behav 103:69–78

    Article  CAS  PubMed  Google Scholar 

  22. Carroll ME, Meisch R (2011) Chapter 9. Acquisition of drug abuse. In: Olmstead M (ed) Animal models of drug addiction, neuromethods. Springer Science + Business Media, Inc

    Google Scholar 

  23. Carroll ME et al (2002) Intravenous cocaine and heroin self-administration in rats selectively bred for differential saccharin intake: phenotype and sex differences. Psychopharmacology 161:304–313

    Article  CAS  PubMed  Google Scholar 

  24. Perry JL et al (2005) Impulsivity (delay discounting) as a predictor of acquisition of IV cocaine self-administration in female rats. Psychopharmacology 178:193–201

    Article  CAS  PubMed  Google Scholar 

  25. Anker JJ et al (2009) Impulsivity predicts the escalation of cocaine self-administration in rats. Pharmacol Biochem Behav 93:343–348

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Perry JL et al (2006) Escalation of i.v. cocaine self-administration and reinstatement of cocaine-seeking behavior in rats bred for high and low saccharin intake. Psychopharmacology 186:235–245

    Article  CAS  PubMed  Google Scholar 

  27. Roth ME, Carroll ME (2004) Sex differences in the escalation of intravenous cocaine intake following long- or short-access to cocaine self-administration. Pharmacol Biochem Behav 78:199–207

    Article  CAS  PubMed  Google Scholar 

  28. Piazza PV et al (1990) Individual reactivity to novelty predicts probability of amphetamine self-administration. Behav Pharmacol 1:339–345

    Article  PubMed  Google Scholar 

  29. Peryhe V et al (1993) Individual differences in the psychomotor effects of morphine are predicted by reactivity to novelty and influenced by corticosterone secretion. Brain Res 623:341–344

    Article  Google Scholar 

  30. Economidou D et al (2009) High impulsivity predicts relapse to cocaine-seeking after punishment-induced abstinence. Biol Psychiatry 65:851–856

    Article  CAS  PubMed  Google Scholar 

  31. Stead JD et al (2006) Selective breeding for divergence in novelty-seeking traits: heritability and enrichment in spontaneous anxiety-related behaviors. Behav Genet 36:697–712

    Article  PubMed  Google Scholar 

  32. Saunders BT, Robinson TE (2011) Individual variation in the motivational properties of cocaine. Neuropsychopharmacology 36:1668–1676

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Larson EB, Carroll ME (2005) Wheel running as a predictor of cocaine self-administration and reinstatement in female rats. Pharmacol Biochem Behav 82:590–600

    Article  CAS  PubMed  Google Scholar 

  34. Lovic V et al (2011) Rats prone to attribute incentive salience to reward cues are also prone to impulsive action. Behav Brain Res 223:255–261

    Article  PubMed  PubMed Central  Google Scholar 

  35. Flagel SB et al (2008) Individual differences in the attribution of incentive salience to a reward-related cue: influence on cocaine sensitization. Behav Brain Res 186:48–56

    Article  CAS  PubMed  Google Scholar 

  36. Dalley JW et al (2005) Attentional and motivational deficits in rats withdrawn from intravenous self-administration of cocaine or heroin. Psychopharmacology 182:579–587

    Article  CAS  PubMed  Google Scholar 

  37. Anker JJ et al (2009) Effects of allopregnanolone on the reinstatement of cocaine-seeking behavior in male and female rats. Psychopharmacology 203:63–72

    Article  CAS  PubMed  Google Scholar 

  38. Poulos CX, Le AD, Parker JL (1995) Impulsivity predicts individual susceptibility to high levels of alcohol self-administration. Behav Pharmacol 6:810–814

    Article  PubMed  Google Scholar 

  39. Perry JL, Nelson SE, Carroll ME (2008) Impulsive choice as a predictor of acquisition of IV cocaine self- administration and reinstatement of cocaine-seeking behavior in male and female rats. Exp Clin Psychopharmacol 16:165–177

    Article  PubMed  Google Scholar 

  40. Mardones J, Segovia N, Hederra A (1953) Heredity of experimental alcohol preference in rats. II. Coefficient of heredity. Q J Stud Alcohol 14:1–2

    Article  CAS  PubMed  Google Scholar 

  41. Crabbe JC (1984) Pharmacogenetic strategies for studying alcohol dependence. Alcohol 1:185–191

    Article  CAS  PubMed  Google Scholar 

  42. Li TK, Lumeng L, Doolittle DP (1993) Selective breeding for alcohol preference and associated responses. Behav Genet 23:163–170

    Article  CAS  PubMed  Google Scholar 

  43. Foroud T et al (2000) Identification of quantitative trait loci influencing alcohol consumption in the high alcohol drinking and low alcohol drinking rat lines. Behav Genet 30:131–140

    Article  CAS  PubMed  Google Scholar 

  44. McBride WJ, Li TK (1998) Animal models of alcoholism: neurobiology of high alcohol-drinking behavior in rodents. Crit Rev Neurobiol 12:339–369

    Article  CAS  PubMed  Google Scholar 

  45. Crabbe JC et al (1985) Bidirectional selection for susceptibility to ethanol withdrawal seizures in Mus musculus. Behav Genet 15:521–536

    Article  CAS  PubMed  Google Scholar 

  46. Cunningham CL et al (1991) Assessment of ethanol’s hedonic effects in mice selectively bred for sensitivity to ethanol-induced hypothermia. Psychopharmacology 105:84–92

    Article  CAS  PubMed  Google Scholar 

  47. Phillips TJ, Dudek BC (1991) Locomotor activity responses to ethanol in selectively bred long- and short-sleep mice, two inbred mouse strains, and their F1 hybrids. Alcohol Clin Exp Res 15:255–261

    Article  CAS  PubMed  Google Scholar 

  48. Gallaher EJ et al (1987) Mouse lines selected for genetic differences in diazepam sensitivity. Psychopharmacology 93:25–30

    Article  CAS  PubMed  Google Scholar 

  49. Belknap JK et al (1983) Selective breeding for high and low levels of opiate-induced analgesia in mice. Behav Genet 13:383–396

    Article  CAS  PubMed  Google Scholar 

  50. Atkins AL et al (2001) Stereotypic behaviors in mice selectively bred for high and low methamphetamine-induced stereotypic chewing. Psychopharmacology 157:96–104

    Article  CAS  PubMed  Google Scholar 

  51. Wheeler JM et al (2009) Genetically correlated effects of selective breeding for high and low methamphetamine consumption. Genes Brain Behav 8:758–771

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Smolen A et al (1994) Individual differences in sensitivity to nicotine in mice: response to six generations of selective breeding. Pharmacol Biochem Behav 49:531–540

    Article  CAS  PubMed  Google Scholar 

  53. He S et al (2008) Selective breeding for intravenous drug self-administration in rats: a pilot study. Behav Pharmacol 19:751–764

    Article  CAS  PubMed  Google Scholar 

  54. Oberlin BG, Grahame NJ (2009) High-alcohol preferring mice are more impulsive than low-alcohol preferring mice as measured in the delay discounting task. Alcohol Clin Exp Res 33:1294–1303

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Wilhelm CJ et al (2007) Mouse lines selected for alcohol consumption differ on certain measures of impulsivity. Alcohol Clin Exp Res 31:1839–1845

    Article  PubMed  CAS  Google Scholar 

  56. Riley EP et al (1977) Selective breeding of rats for differences in reactivity to alcohol. An approach to an animal model of alcoholism. II. Behavioral measures. J Stud Alcohol 38:1705–1717

    Article  CAS  PubMed  Google Scholar 

  57. Dess NK et al (1998) Ethanol consumption in rats selectively bred for differential saccharin intake. Alcohol 16:275–278

    Article  CAS  PubMed  Google Scholar 

  58. Belin D et al (2008) High impulsivity predicts the switch to compulsive cocaine-taking. Science 320:1352–1355

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Perry JL, Carroll ME (2008) The role of impulsive behavior in drug abuse. Psychopharmacology 200:1–26

    Article  CAS  PubMed  Google Scholar 

  60. Klebaur JE et al (2001) Individual differences in behavioral responses to novelty and amphetamine self-administration in male and female rats. Behav Pharmacol 12:267–275

    Article  CAS  PubMed  Google Scholar 

  61. Diergaarde L et al (2009) Trait impulsivity predicts escalation of sucrose seeking and hypersensitivity to sucrose-associated stimuli. Behav Neurosci 123:794–803

    Article  CAS  PubMed  Google Scholar 

  62. Fernandez-Teruel A et al (2002) Enduring effects of environmental enrichment on novelty seeking, saccharin and ethanol intake in two rat lines (RHA/Verh and RLA/Verh) differing in incentive-seeking behavior. Pharmacol Biochem Behav 73:225–231

    Article  CAS  PubMed  Google Scholar 

  63. Razafimanalina R, Mormede P, Velley L (1996) Gustatory preference-aversion profiles for saccharin, quinine and alcohol in Roman high- and low-avoidance lines. Behav Pharmacol 7:78–84

    Article  CAS  PubMed  Google Scholar 

  64. Grahame NJ, Li TK, Lumeng L (1999) Selective breeding for high and low alcohol preference in mice. Behav Genet 29:47–57

    Article  CAS  PubMed  Google Scholar 

  65. Stewart RB et al (1994) Consumption of sweet, salty, sour, and bitter solutions by selectively bred alcohol-preferring and alcohol-nonpreferring lines of rats. Alcohol Clin Exp Res 18:375–381

    Article  CAS  PubMed  Google Scholar 

  66. Sinclair JD et al (1992) Taste preferences in rat lines selected for low and high alcohol consumption. Alcohol 9:155–160

    Article  CAS  PubMed  Google Scholar 

  67. Overstreet DH et al (1993) Saccharin intake predicts ethanol intake in genetically heterogeneous rats as well as different rat strains. Alcohol Clin Exp Res 17:366–369

    Article  CAS  PubMed  Google Scholar 

  68. Gahtan E et al (1996) The relationships among saccharin consumption, oral ethanol, and i.v. cocaine self-administration. Pharmacol Biochem Behav 53:919–925

    Article  CAS  PubMed  Google Scholar 

  69. DeSousa NJ, Bush DE, Vaccarino FJ (2000) Self-administration of intravenous amphetamine is predicted by individual differences in sucrose feeding in rats. Psychopharmacology 148:52–58

    Article  CAS  PubMed  Google Scholar 

  70. Gosnell BA et al (1995) Intravenous morphine self-administration by rats with low versus high saccharin preferences. Psychopharmacology 117:248–252

    Article  CAS  PubMed  Google Scholar 

  71. Janowsky DS, Pucilowski O, Buyinza M (2003) Preference for higher sucrose concentrations in cocaine abusing-dependent patients. J Psychiatr Res 37:35–41

    Article  PubMed  Google Scholar 

  72. Pomerleau CS et al (1991) Sweet taste preference in women smokers: comparison with nonsmokers and effects of menstrual phase and nicotine abstinence. Pharmacol Biochem Behav 40:995–999

    Article  CAS  PubMed  Google Scholar 

  73. Pepino MY, Mennella JA (2007) Effects of cigarette smoking and family history of alcoholism on sweet taste perception and food cravings in women. Alcohol Clin Exp Res 31:1891–1899

    Article  PubMed  PubMed Central  Google Scholar 

  74. Weiss G (1982) Food fantasies of incarcerated drug users. Int J Addict 17:905–912

    Article  CAS  PubMed  Google Scholar 

  75. Wronski M et al (2007) Perceived intensity and pleasantness of sucrose taste in male alcoholics. Alcohol Alcohol 42:75–79

    Article  PubMed  Google Scholar 

  76. Kampov-Polevoy A, Garbutt JC, Janowsky D (1997) Evidence of preference for a high-concentration sucrose solution in alcoholic men. Am J Psychiatry 154:269–270

    Article  CAS  PubMed  Google Scholar 

  77. Kampov-Polevoy AB et al (2001) Sweet liking and family history of alcoholism in hospitalized alcoholic and non-alcoholic patients. Alcohol Alcohol 36:165–170

    Article  CAS  PubMed  Google Scholar 

  78. Uhl GR et al (2009) Addiction genetics and pleiotropic effects of common haplotypes that make polygenic contributions to vulnerability to substance dependence. J Neurogenet 23:272–282

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Keskitalo K et al (2007) Same genetic components underlie different measures of sweet taste preference. Am J Clin Nutr 86:1663–1669

    Article  CAS  PubMed  Google Scholar 

  80. Keskitalo K et al (2008) The Three-Factor Eating Questionnaire, body mass index, and responses to sweet and salty fatty foods: a twin study of genetic and environmental associations. Am J Clin Nutr 88:263–271

    Article  CAS  PubMed  Google Scholar 

  81. Keskitalo K et al (2007) Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16. Am J Clin Nutr 86:55–63

    Article  CAS  PubMed  Google Scholar 

  82. Reed DR et al (1997) Heritable variation in food preferences and their contribution to obesity. Behav Genet 27:373–387

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. Bachmanov AA et al (2011) Genetics of sweet taste preferences. Flavour Fragr J 26:286–294

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. Lu K et al (2005) No relationship between sequence variation in protein coding regions of the Tas1r3 gene and saccharin preference in rats. Chem Senses 30:231–240

    Article  CAS  PubMed  Google Scholar 

  85. Kampov-Polevoy AB, Garbutt JC, Khalitov E (2003) Family history of alcoholism and response to sweets. Alcohol Clin Exp Res 27:1743–1749

    Article  PubMed  Google Scholar 

  86. Nachman M (1959) The inheritance of saccharin preference. J Comp Physiol Psychol 52:451–457

    Article  CAS  PubMed  Google Scholar 

  87. Pelz WE, Whitney G, Smith JC (1973) Genetic influences on saccharin preference of mice. Physiol Behav 10:263–265

    Article  CAS  PubMed  Google Scholar 

  88. Ramirez I, Fuller JL (1976) Genetic influence on water and sweetened water consumption in mice. Physiol Behav 16:163–168

    Article  CAS  PubMed  Google Scholar 

  89. Lush IE (1989) The genetics of tasting in mice. VI. Saccharin, acesulfame, dulcin and sucrose. Genet Res 53:95–99

    Article  CAS  PubMed  Google Scholar 

  90. Capeless CG, Whitney G (1995) The genetic basis of preference for sweet substances among inbred strains of mice: preference ratio phenotypes and the alleles of the Sac and dpa loci. Chem Senses 20:291–298

    Article  CAS  PubMed  Google Scholar 

  91. Dess NK, Minor TR (1996) Taste and emotionality in rats selectively bred for high versus low saccharin intake. Anim Learn Behav 24:105–155

    Article  Google Scholar 

  92. Holtz NA, Carroll ME (2011) Baclofen has opposite effects on escalation of cocaine self-administration: increased intake in rats selectively bred for high (HiS) saccharin intake and decreased intake in those selected for low (LoS) saccharin intake. Pharmacol Biochem Behav 100:275–283

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Anker JJ et al (2012) Escalation of methamphetamine self-administration in adolescent and adult rats. Drug Alcohol Depend:149–153

    Google Scholar 

  94. Anker JJ, Carroll ME (2011) Adolescent nicotine exposure sensitizes cue-induced reinstatement of cocaine seeking in rats bred for high and low saccharin intake. Drug Alcohol Depend 118:68–72

    Article  CAS  PubMed  Google Scholar 

  95. Carroll ME, Anderson MM, Morgan AD (2007) Higher locomotor response to cocaine in female (vs. male) rats selectively bred for high (HiS) and low (LoS) saccharin intake. Pharmacol Biochem Behav 88:94–104

    Article  CAS  PubMed  Google Scholar 

  96. Anker JJ, Gliddon LA, Carroll ME (2008) Impulsivity on a Go/No-go task for intravenous cocaine or food in male and female rats selectively bred for high and low saccharin intake. Behav Pharmacol 19:615–629

    Article  CAS  PubMed  Google Scholar 

  97. Perry JL et al (2007) Impulsivity (delay discounting) for food and cocaine in male and female rats selectively bred for high and low saccharin intake. Pharmacol Biochem Behav 86:822–837

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  98. Carroll ME et al (2010) Delay discounting as a predictor of drug abuse. In: Madden GJ, Bickel WK (eds) Impulsivity: the behavioral and neurological science of discounting. American Psychological Association, Washington, DC

    Google Scholar 

  99. de Wit H (2009) Impulsivity as a determinant and consequence of drug use: a review of underlying processes. Addict Biol 14:22–31

    Article  PubMed  Google Scholar 

  100. Winstanley CA et al (2010) Insight into the relationship between impulsivity and substance abuse from studies using animal models. Alcohol Clin Exp Res 34:1306–1318

    PubMed  PubMed Central  Google Scholar 

  101. Winstanley CA et al (2010) Dopaminergic modulation of the orbitofrontal cortex affects attention, motivation and impulsive responding in rats performing the five-choice serial reaction time task. Behav Brain Res 210:263–272

    Article  CAS  PubMed  Google Scholar 

  102. Dalley JW et al (2007) Nucleus accumbens D2/3 receptors predict trait impulsivity and cocaine reinforcement. Science 315:1267–1270

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  103. Anker JJ et al (2011) Responding during signaled availability and nonavailability of iv cocaine and food in rats: age and sex differences. Psychopharmacology 215:785–799

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  104. Wilmouth CE, Spear LP (2009) Hedonic sensitivity in adolescent and adult rats: taste reactivity and voluntary sucrose consumption. Pharmacol Biochem Behav 92:566–573

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  105. Vaidya JG et al (2004) A comparative developmental study of impulsivity in rats and humans: the role of reward sensitivity. Ann N Y Acad Sci 1021:395–398

    Article  PubMed  Google Scholar 

  106. Cummins E, Leri F (2008) Unreinforced responding during limited access to heroin self-administration. Pharmacol Biochem Behav 90:420–427

    Article  CAS  PubMed  Google Scholar 

  107. Kosten TA, Zhang XY, Haile CN (2007) Strain differences in maintenance of cocaine self-administration and their relationship to novelty activity responses. Behav Neurosci 121:380–388

    Article  CAS  PubMed  Google Scholar 

  108. Flagel SB et al (2010) An animal model of genetic vulnerability to behavioral disinhibition and responsiveness to reward-related cues: implications for addiction. Neuropsychopharmacology 35:388–400

    Article  PubMed  Google Scholar 

  109. Carroll ME (1985) The role of food deprivation in the maintenance and reinstatement of cocaine-seeking behavior in rats. Drug Alcohol Depend 16:95–109

    Article  CAS  PubMed  Google Scholar 

  110. Cummings JA et al (2011) Effects of a selectively bred novelty-seeking phenotype on the motivation to take cocaine in male and female rats. Biol Sex Differ 2:3

    Article  PubMed  PubMed Central  Google Scholar 

  111. Furudono Y et al (2006) Involvement of specific orexigenic neuropeptides in sweetener-induced overconsumption in rats. Behav Brain Res 175:241–248

    Article  CAS  PubMed  Google Scholar 

  112. Borgland SL et al (2009) Orexin A/hypocretin-1 selectively promotes motivation for positive reinforcers. J Neurosci 29:11215–11225

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  113. Espana RA et al (2010) The hypocretin-orexin system regulates cocaine self-administration via actions on the mesolimbic dopamine system. Eur J Neurosci 31:336–348

    Article  PubMed  Google Scholar 

  114. Dess NK et al (2000) Exploring adaptations to famine: rats selectively bred for differential intake of saccharin differ on deprivation-induced hyperactivity and emotionality. Int J Comp Psychol 13:34–52

    Article  Google Scholar 

  115. Evans BE et al (2012) The relation between HPA axis activity and age of onset of alcohol use. Addiction 107:312–322

    Article  PubMed  Google Scholar 

  116. Sinha R (2008) Chronic stress, drug use, and vulnerability to addiction. Ann N Y Acad Sci 1141:105–130

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  117. Ungless MA, Argilli E, Bonci A (2010) Effects of stress and aversion on dopamine neurons: implications for addiction. Neurosci Biobehav Rev 35:151–156

    Article  CAS  PubMed  Google Scholar 

  118. Koda K et al (2010) Effects of acute and chronic administration of atomoxetine and methylphenidate on extracellular levels of noradrenaline, dopamine and serotonin in the prefrontal cortex and striatum of mice. J Neurochem 114:259–270

    CAS  PubMed  Google Scholar 

  119. Schreiber HL, Wood GW, Carlson RH (1976) The role of locomotion in conditioning methylphenidate-induced locomotor activity. Pharmacol Biochem Behav 4:393–395

    Article  CAS  PubMed  Google Scholar 

  120. Lang PJ, Davis M, Ohman A (2000) Fear and anxiety: animal models and human cognitive psychophysiology. J Affect Disord 61:137–159

    Article  CAS  PubMed  Google Scholar 

  121. Morgan CA 3rd et al (1993) Yohimbine-facilitated acoustic startle reflex in humans. Psychopharmacology 110:342–346

    Article  CAS  PubMed  Google Scholar 

  122. Davis M (1992) The role of the amygdala in fear-potentiated startle: implications for animal models of anxiety. Trends Pharmacol Sci 13:35–41

    Article  CAS  PubMed  Google Scholar 

  123. Vaidyanathan U, Patrick CJ, Cuthbert BN (2009) Linking dimensional models of internalizing psychopathology to neurobiological systems: affect-modulated startle as an indicator of fear and distress disorders and affiliated traits. Psychol Bull 135:909–942

    Article  PubMed  PubMed Central  Google Scholar 

  124. Gonzales M et al (2008) Stress-induced attenuation of acoustic startle in low-saccharin-consuming rats. Biol Psychol 79:193–199

    Article  PubMed  Google Scholar 

  125. Koob GF, Volkow ND (2010) Neurocircuitry of addiction. Neuropsychopharmacology 35:217–238

    Article  PubMed  Google Scholar 

  126. Dess NK, O’Neill P, Chapman CD (2005) Ethanol withdrawal and proclivity are inversely related in rats selectively bred for differential saccharin intake. Alcohol 37:9–22

    Article  CAS  PubMed  Google Scholar 

  127. Blumenthal DM, Gold MS (2010) Neurobiology of food addiction. Curr Opin Clin Nutr Metab Care 13:359–365

    Article  PubMed  Google Scholar 

  128. Avena NM, Rada P, Hoebel BG (2006) Sugar bingeing in rats. Curr Protoc Neurosci Chapter 9, Unit9 23C

    Google Scholar 

  129. Avena NM, Long KA, Hoebel BG (2005) Sugar-dependent rats show enhanced responding for sugar after abstinence: evidence of a sugar deprivation effect. Physiol Behav 84:359–362

    Article  CAS  PubMed  Google Scholar 

  130. Negus SS (2005) Effects of punishment on choice between cocaine and food in rhesus monkeys. Psychopharmacology 181:244–252

    Article  CAS  PubMed  Google Scholar 

  131. Woolverton WL et al (2012) Suppression of cocaine self-administration in monkeys: effects of delayed punishment. Psychopharmacology 220:509–517

    Article  CAS  PubMed  Google Scholar 

  132. Sershen H, Hashim A, Lajtha A (1998) Gender differences in kappa-opioid modulation of cocaine-induced behavior and NMDA-evoked dopamine release. Brain Res 801:67–71

    Article  CAS  PubMed  Google Scholar 

  133. Cosgrove KP, Carroll ME (2004) Differential effects of bremazocine on oral phencyclidine (PCP) self-administration in male and female rhesus monkeys. Exp Clin Psychopharmacol 12:111–117

    Article  CAS  PubMed  Google Scholar 

  134. Campbell UC, Morgan AD, Carroll ME (2002) Sex differences in the effects of baclofen on the acquisition of intravenous cocaine self-administration in rats. Drug Alcohol Depend 66:61–69

    Article  CAS  PubMed  Google Scholar 

  135. Carroll ME, Campbell UC, Heideman P (2001) Ketoconazole suppresses food restriction-induced increases in heroin self-administration in rats: sex differences. Exp Clin Psychopharmacol 9:307–316

    Article  CAS  PubMed  Google Scholar 

  136. Cosgrove KP, Hunter RG, Carroll ME (2002) Wheel-running attenuates intravenous cocaine self-administration in rats: sex differences. Pharmacol Biochem Behav 73:663–671

    Article  CAS  PubMed  Google Scholar 

  137. Cosgrove KP, Carroll ME (2003) Effects of a non-drug reinforcer, saccharin, on oral self-administration of phencyclidine in male and female rhesus monkeys. Psychopharmacology 170:9–16

    Article  CAS  PubMed  Google Scholar 

  138. Anker JJ, Carroll ME (2011) Females are more vulnerable to drug abuse than males: evidence from preclinical studies and the role of ovarian hormones. Curr Top Behav Neurosci 8:73–96

    Article  CAS  PubMed  Google Scholar 

  139. Carroll ME et al (2004) Sex and estrogen influence drug abuse. Trends Pharmacol Sci 25:273–279

    Article  CAS  PubMed  Google Scholar 

  140. Mello NK (2010) Hormones, nicotine, and cocaine: clinical studies. Horm Behav 58:57–71

    Article  CAS  PubMed  Google Scholar 

  141. Garbutt JC et al (2009) Sweet liking phenotype, alcohol craving and response to naltrexone treatment in alcohol dependence. Alcohol Alcohol 44:293–300

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  142. Carroll ME et al (2005) Sex differences in the escalation of oral phencyclidine (PCP) self-administration under FR and PR schedules in rhesus monkeys. Psychopharmacology 180:414–426

    Article  CAS  PubMed  Google Scholar 

  143. Hansen ST, Mark GP (2007) The nicotinic acetylcholine receptor antagonist mecamylamine prevents escalation of cocaine self-administration in rats with extended daily access. Psychopharmacology 194:53–61

    Article  CAS  PubMed  Google Scholar 

  144. Specio SE et al (2008) CRF(1) receptor antagonists attenuate escalated cocaine self-administration in rats. Psychopharmacology 196:473–482

    Article  CAS  PubMed  Google Scholar 

  145. Smith MA et al (2004) Effects of positive allosteric modulators of the GABAB receptor on cocaine self-administration in rats. Psychopharmacology 173:105–111

    Article  CAS  PubMed  Google Scholar 

  146. Karila L et al (2008) New treatments for cocaine dependence: a focused review. Int J Neuropsychopharmacol 11:425–438

    Article  CAS  PubMed  Google Scholar 

  147. Leggio L, Garbutt JC, Addolorato G (2010) Effectiveness and safety of baclofen in the treatment of alcohol dependent patients. CNS Neurol Disord Drug Targets 9:33–44

    Article  CAS  PubMed  Google Scholar 

  148. Roberts DC (2005) Preclinical evidence for GABAB agonists as a pharmacotherapy for cocaine addiction. Physiol Behav 86:18–20

    Article  CAS  PubMed  Google Scholar 

  149. Fadda P et al (2003) Baclofen antagonizes nicotine-, cocaine-, and morphine-induced dopamine release in the nucleus accumbens of rat. Synapse 50:1–6

    Article  CAS  PubMed  Google Scholar 

  150. Campbell UC, Lac ST, Carroll ME (1999) Effects of baclofen on maintenance and reinstatement of intravenous cocaine self-administration in rats. Psychopharmacology 143:209–214

    Article  CAS  PubMed  Google Scholar 

  151. Filip M, Frankowska M (2007) Effects of GABA(B) receptor agents on cocaine priming, discrete contextual cue and food induced relapses. Eur J Pharmacol 571:166–173

    Article  CAS  PubMed  Google Scholar 

  152. Weerts EM et al (2007) Attenuation of cocaine-seeking by GABA B receptor agonists baclofen and CGP44532 but not the GABA reuptake inhibitor tiagabine in baboons. Drug Alcohol Depend 89:206–213

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  153. Kahn R et al (2009) Multi-center trial of baclofen for abstinence initiation in severe cocaine-dependent individuals. Drug Alcohol Depend 103:59–64

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  154. Berner LA et al (2009) Baclofen suppresses binge eating of pure fat but not a sugar-rich or sweet-fat diet. Behav Pharmacol 20:631–634

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  155. Anker JJ, Carroll ME (2010) The role of progestins in the behavioral effects of cocaine and other drugs of abuse: human and animal research. Neurosci Biobehav Rev 35:315–333

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  156. Sofuoglu M, Mitchell E, Mooney M (2009) Progesterone effects on subjective and physiological responses to intravenous nicotine in male and female smokers. Hum Psychopharmacol 24:559–564

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  157. Sofuoglu M, Mouratidis M, Mooney M (2011) Progesterone improves cognitive performance and attenuates smoking urges in abstinent smokers. Psychoneuroendocrinology 36:123–132

    Article  CAS  PubMed  Google Scholar 

  158. Gosnell BA et al (2010) Operant responding for sucrose by rats bred for high or low saccharin consumption. Physiol Behav 99:529–533

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  159. Dess NK, Chapman CD, Monroe D (2009) Consumption of SC45647 and sucralose by rats selectively bred for high and low saccharin intake. Chem Senses 34:211–220

    Article  CAS  PubMed  Google Scholar 

  160. Dess NK (2000) Responses to basic taste qualities in rats selectively bred for high versus low saccharin intake. Physiol Behav 69:247–257

    Article  CAS  PubMed  Google Scholar 

  161. De Francisco JC, Dess NK (1998) Aspartame consumption in rats selectively bred for high versus low saccharin intake. Physiol Behav 65:393–396

    Article  PubMed  Google Scholar 

  162. Czachowski CL, Delory MJ (2009) Acamprosate and naltrexone treatment effects on ethanol and sucrose seeking and intake in ethanol-dependent and nondependent rats. Psychopharmacology 204:335–348

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  163. Burdick KE, Gopin CB, Malhotra AK (2010) Pharmacogenetic approaches to cognitive enhancement in schizophrenia. Harv Rev Psychiatry 19:102–108

    Article  Google Scholar 

  164. Schosser A, Kasper S (2009) The role of pharmacogenetics in the treatment of depression and anxiety disorders. Int Clin Psychopharmacol 24:277–288

    Article  PubMed  Google Scholar 

  165. Kieling C et al (2010) A current update on ADHD pharmacogenomics. Pharmacogenomics 11:407–419

    Article  CAS  PubMed  Google Scholar 

  166. Sturgess JE et al (2011) Pharmacogenetics of alcohol, nicotine and drug addiction treatments. Addict Biol 16:357–376

    Article  CAS  PubMed  Google Scholar 

  167. Anton RF et al (2008) An evaluation of mu-opioid receptor (OPRM1) as a predictor of naltrexone response in the treatment of alcohol dependence: results from the Combined Pharmacotherapies and Behavioral Interventions for Alcohol Dependence (COMBINE) study. Arch Gen Psychiatry 65:135–144

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  168. Oroszi G et al (2009) OPRM1 Asn40Asp predicts response to naltrexone treatment: a haplotype-based approach. Alcohol Clin Exp Res 33:383–393

    Article  CAS  PubMed  Google Scholar 

  169. Setiawan E et al (2011) The effect of naltrexone on alcohol’s stimulant properties and self-administration behavior in social drinkers: influence of gender and genotype. Alcohol Clin Exp Res 35:1134–1141

    Article  CAS  PubMed  Google Scholar 

  170. Vallender EJ et al (2010) A pharmacogenetic model of naltrexone-induced attenuation of alcohol consumption in rhesus monkeys. Drug Alcohol Depend 109:252–256

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  171. Flagel SB, Akil H, Robinson TE (2009) Individual differences in the attribution of incentive salience of reward-related cues: implications for addiction. Neuropharmacology 56:139–148

    Article  CAS  PubMed  Google Scholar 

  172. Wilhelm CJ, Mitchell SH (2008) Rats bred for high alcohol drinking are more sensitive to delayed and probabilistic outcomes. Genes Brain Behav 7:705–713

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  173. Fattore L et al (2009) The Roman high- and low-avoidance rat lines differ in the acquisition, maintenance, extinction, and reinstatement of intravenous cocaine self-administration. Neuropsychopharmacology 34:1091–1101

    Article  CAS  PubMed  Google Scholar 

  174. Moreno M et al (2010) Impulsivity characterization in the Roman high- and low- avoidance rat strains: behavioral and neurochemical differences. Neuropsychopharmacology 35:1198–1208

    Article  PubMed  PubMed Central  Google Scholar 

  175. Haile CN et al (2001) Differential behavioral responses to cocaine are associated with dynamics of mesolimbic dopamine proteins in Lewis and Fischer 344 rats. Synapse 41:179–190

    Article  CAS  PubMed  Google Scholar 

  176. Suzuki T, George FR, Meisch RA (1988) Differential establishment and maintenance of oral ethanol reinforced behavior in Lewis and Fischer 344 inbred rat strains. J Pharmacol Exp Ther 245:164–170

    CAS  PubMed  Google Scholar 

  177. Kosten TA et al (1994) Fischer and Lewis rat strains show differential cocaine effects in conditioned place preference and behavioral sensitization but not in locomotor activity or conditioned taste aversion. J Pharmacol Exp Ther 269:137–144

    CAS  PubMed  Google Scholar 

  178. Kruzich PJ, Xi J (2006) Different patterns of pharmacological reinstatement of cocaine-seeking behavior between Fischer 344 and Lewis rats. Psychopharmacology 187:22–29

    Article  CAS  PubMed  Google Scholar 

  179. Perry JL et al (2007) Acquisition of i.v. cocaine self-administration in adolescent and adult male rats selectively bred for high and low saccharin intake. Physiol Behav 91:126–133

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  180. Carroll ME, Anderson MM, Morgan AD (2007) Regulation of intravenous cocaine self-administration in rats selectively bred for high (HiS) and low (LoS) saccharin intake. Psychopharmacology 190:331–341

    Article  CAS  PubMed  Google Scholar 

  181. Dellu F et al (1996) Behavioral reactivity to novelty during youth as a predictive factor of stress-induced corticosterone secretion in the elderly- a life-span study in rats. Psychoneuroendocrinology 21:441–453

    Article  CAS  PubMed  Google Scholar 

  182. Kabbaj M et al (2000) Neurobiological correlates of individual differences in novelty- seeking behavior in the rat: differential expression of stress-related molecules. J Neurosci 20:6938–6988

    Article  Google Scholar 

  183. Chester JA, Blose AM, Froehlich JC (2003) Further evidence of an inverse genetic relationship between innate differences in alcohol preference and alcohol withdrawal magnitude in multiple selectively bred rat lines. Alcohol Clin Exp Res 27:377–387

    Article  PubMed  Google Scholar 

  184. Kosten TA, Ambrosio E (2002) HPA axis function and drug addictive behaviors: insights from studies with Lewis and Fischer 344 inbred rats. Psychoneuroendocrinology 27:35–69

    Article  CAS  PubMed  Google Scholar 

  185. Anker JJ et al (2012) Escalation of methamphetamine self-administration in adolescent and adult rats. Drug Alcohol Depend 124:149–153

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  186. Venniro M, Caprioli D, Shaham Y (2018) Novel models of drug relapse and craving after voluntary abstinence. Neuropsychopharmacology 44:214–236

    Google Scholar 

  187. Carroll ME et al (1979) Food deprivation increases oral and intravenous drug intake in rats. Science 205:319–321

    Article  CAS  PubMed  Google Scholar 

  188. Carroll ME et al (1981) Intravenous self-administration of etonitazene, cocaine and phencyclidine in rats during food deprivation and satiation. J Pharmacol Exp Ther 217:241–247

    CAS  PubMed  Google Scholar 

  189. Carroll ME (1985) The role of food deprivation in the maintenance and reinstatement of cocaine-seeking behavior in rats. Dr Alc Dep 16:95–109

    Article  CAS  Google Scholar 

  190. Larson EB, Carroll ME (2005) Wheel running as a predictor of cocaine self- administration and reinstatement in female rats. Pharmacol Biochem Behav 82:590–600

    Article  CAS  PubMed  Google Scholar 

  191. Cosgrove KP et al (2002) Effects of bremazocine on the self-administration of smoked cocaine base and orally delivered ethanol, phencyclidine, saccharin and food in rhesus monkeys: a behavioral economic analysis. J Pharmacol Exp Ther 301:993–1002

    Article  CAS  PubMed  Google Scholar 

  192. Zlebnik NE et al (2012) Exercise to reduce the escalation of cocaine self-administration in adolescent and adult rats. Psychopharmacology 224:387–400

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  193. Zlebnik NE, Carroll ME (2015) Effects of the combination of wheel running and atomoxetine on cue- and cocaine-primed reinstatement in rats selected for high or low impulsivity. Psychopharmacology 232:1049–1059

    Article  CAS  PubMed  Google Scholar 

  194. Zlebnik NE, Carroll ME (2015) Prevention of incubation of cocaine seeking by physical exercise in female rats. Psychopharmacology 232:3577–3413

    Article  Google Scholar 

  195. Carroll ME et al (2019) Preventing incubation of cocaine craving with voluntary aerobic exercise in rats: sex differences. Psychopharmacology (pending revision)

    Google Scholar 

  196. Zlebnik NE et al (2014b) Chronic wheel running affects cocaine-induced c-Fos expression in brain reward areas in rats. Behav Brain Res 261:71–78

    Article  CAS  PubMed  Google Scholar 

  197. Carroll ME et al (1989) A concurrently available nondrug reinforcer prevents the acquisition or decreases the maintenance of cocaine-reinforced behavior. Psychopharmacology 97:23–29

    Article  CAS  PubMed  Google Scholar 

  198. Rawson RA et al (2015) Impact of an exercise intervention on methamphetamine use outcomes post-residential treatment care. Dr Alc Dep 156:21–28

    Article  Google Scholar 

  199. Venniro M et al (2017) Incubation of methamphetamine but not heroin craving after voluntary abstinence in male and female rats. Neuropsychopharmacology 42:1126–1135

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  200. Venniro M et al (2018) Volitional social interaction prevents drug addiction in rat models. Nat Neurosci 21:1520–1529

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  201. Venniro M et al (2019) Operant social reward decreases incubation of heroin craving in male and female rats. Biol Psychiatry 86(11):848–856

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Carroll, M.E., Zlebnik, N.E., Holtz, N.A. (2021). Preference for Palatable Food, Impulsivity, and Relation to Drug Addiction in Rats. In: Avena, N.M. (eds) Animal Models of Eating Disorders. Neuromethods, vol 161. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-0924-8_12

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