Hypolipidemic Activity of Mimosa Pudica

Download as pdf or txt
Download as pdf or txt
You are on page 1of 4

Asian J. Res. Pharm. Sci. 2011; Vol. 1: Issue 4, Pg 124-127 [AJPSci.

ISSN- 2231–5640 (Print) www.asianpharmaonline.org


ISSN- 2231–5659 (Online) 0974-3618

RESEARCH ARTICLE
Hypolipidemic activity of Mimosa pudica Linn on Butter Induced
Hyperlipidemia in Rats
A. Sowmya and T. Ananthi*
Department of Biochemistry, S.T.E.T Womens College, Mannagudi- 614001. Thiruvarur District, Tamil Nadu,
India.
*Corresponding Author E-mail: elangani576@gmail.com

ABSTRACT:
The hypolipidemic activity of Mimosa pudica extract was studied on high fat diet induced models of hyperlipidemia in
rats. Hyperlipidemia in experimental rats evidenced by an enhancement in the levels of Cholesterols, Triglycerides,
LDL and VLDL. Ehanol extract showed significant hypolipidemic effect by lowering the serum levels of biochemical
parameters such as significant reduction in the level of serum Cholesterol, TG, LDL, VLDL and increase in HDL level
which was similar to the standard drug Lovastatin. Preliminary phytochemical analysis revealed the presence of
phytoconstituents such as steroids, flavonoids, glycosides, alkaloids and phenolic compounds.

KEYWORDS: High fat diet, Lovastatin, Mimosa pudica, Hyperlipidemia

INTRODUCTION:
Mimosa pudica L. is common plant in moist waste ground The high levels of cholesterol particularly TC, TG and LDL
belongs to family – Mimosaceae. It mainly contains cholesterol is mainly responsible for the onset of CHDs. A
tannins, steroids, triterpenes, alkaloids, glycosides, 20% reduction of blood cholesterol level can decrease about
flavonoids, c-glycoside, flavones (Adikari, 2003).The 31% of CHD incidence, and 33% of its mortality rate. The
extract of Mimosa pudica is used in the treatment of known lipid lowering drugs, such as fibrates, statins and
migraine, insomnia, headache, diarrhea, dysentery, fistula, bile acid sequestrants have many side effects in patients
piles, and fever (Rajendran, 2010).The decoction of M. (Chattopadhyaya,1996). Thus, there is a considerable
pudica antagonized chemically induced seizures in mice. It interest on development of lipid lowering drugs from
significantly protected the mice in PTZ-induced seizures. natural products in the recent years.
Plant is also used as a blood purifier (Ghani, 1998). In
Ayurvedic and Unani system of medicine, this plant has As Mimosa pudica plant species have been traditionally
been used in diseases arising from corrupted blood and bile, claimed for the treatment of atherosclerosis; hence, in the
heart disorders, bilious fever, piles, jaundice, leprosy, ulcers present study, an attempt has been made to screen the
and small pox. herbal extract that is ethanol extract of Mimosa pudica
leaves, for the hypolipidemic activity to prove its claim in
Hyperlipidemia contributes significantly in the folklore practice.
manifestation and development of atherosclerosis and
coronary heart diseases (CHD). Atherosclerosis, are the MATERIALS AND METHODS:
most common cause of mortality and morbidity worldwide. Collection of plant materials:
Although several factors, such as diet high in saturated fats Mimosa pudica whole plants materials were collected from
and cholesterol, age, family history, hypertension and life the fields of Thiruvarur in Tamilnadu.
style play a significant role in causing heart failure
(Blackwelder, 1977). Preparation of plant extract:
Mimosa pudica whole plants were dried at 40ºC for 7 days.
Powered using electric grinder’s server and stored in a
Received on 03.10.2011 Accepted on 21.10.2011 container. This fine cured powered was used as herbal drug.
© Asian Pharma Press All Right Reserved Weighed amount of dried powered of Mimosa pudica
Asian J. Res. Pharm. Sci. 1(4): Oct.-Dec. 2011; Page 124-127 whole plant were taken and added 50 ml of 99.9% hot
124
Asian J. Res. Pharm. Sci. 2011; Vol. 1: Issue 4, Pg 124-127 [AJPSci.]

ethanol mixture and evaporated at 55ºC by using hot air Statistical Analysis:
oven, the collected were for hypolipidemic activity studies. Results were presented as mean ± SD. The significance of
difference among the groups was assessed using one way
Preliminary Phytochemical analysis: analysis of variance (ANOVA) followed by Dunken’s
The ethanol extract of M.pudica was subjected to Multiple Reliance test using SPSS software.P 0.05 was
preliminary phytochemical analysis to assess the presence considered significant.
of various phytoconstituents; it revealed the presence of
flavonoids, alkaloids and glycosides (Harborne,1984). RESULTS:
Healthy young male albino rats (130-150 gm) were The preliminary phytochemical screening revealed the
purchased from animal house of St, Joseph arts and science presence of phytoconstituents such as glycosides, alkaloids,
college, Tirchy. The groups of rats were kept separately flavonoids, tannins, saponins and phenolic compound in the
individual stainless steel hoppers. The test animals should ethanol extract of Mimosa pudica linn. (Table I)
be characterized by strain, source, sex, weight and age. The
animals were kept individually for feeding in conventional
laboratory diets with an unlimited supply of drinking water. Table 1: Phytochemical screening of ethanol extract of Mimosa pudica
S. No Test Constituents of Mimosa pudica
Diagnostics kits: 1. Alkaloids +
Diagnostics kits used for the estimation of lipid profile 2. Carbohydrates -
3. Saponins +
(Totalcholesterol, triglycerides, HDL, VLDL, LDL) were 4. Tannins +
obtained from Eumic laboratory, Trichy. 5. Terpenoids -
6. Flavanoids +
Hyperlipidemic inducer: 7. Phenol +
Butter was used as the hyperlipidemic inducer in animal + indicates presence; - indicates absence
procured from Trichy.400mg of butter/Kg b.wt dissolved in
10ml of buffered saline was used for the induction of
hypolipidemic rats. Hypolipidemic activity:
A marked increase in the level of serum cholesterol,
Experimental Design: triglycerides, LDL and VLDL were found in the animals
Group I was considered as control which received 0.5% which received high fat diet and HDL levels were
sodium carboxy methyl cellulose; Group II was considered decreased. Administrations of ethanol extract at the dose of
as high fat diet group and received the butter diet; Group III 100 mg/kg showed significant reduction in the level of
was considered as test group and received the test extract serum cholesterol, triglyceride, LDL, VLDL and increase in
that is ethanol extract of Mimosa pudica at the dose of 100 HDL level which was similar to the standard Lovastatin,
mg/ Kg body weight per oral along with the high fat diet and are almost near the levels of normal control.
and Group IV was considered as standard group which
received the standard drug Lovastatin (dose of 75 mg/kg A significant percentage reduction of serum cholesterol,
body weight per oral) along with the high fat diet. triglyceride, LDL, VLDL and percentage increase in HDL
in test extract was also comparable with the standard drug.
Sample Collection: A potent hypolipidemic effect of ethanol extract was
At the end of 21 day, blood serum was withdrawn from the evident by a significant reduction in the level of serum
st

retro orbital plexus after overnight fasting for the study of cholesterol, LDL, VLDL and triglycerides in the cholesterol
biochemical parameters. Serum was estimated for the total treated animals and also marked increase in the HDL
cholesterol, triglycerides, LDL, VLDL and HDL Cholesterol level (Table.2).
cholesterol.

Table 2: Effect of Mimosa pudica on biochemical parameters


S. No Groups Total Cholestrol Triglyceride HDL LDL VLDL
(mg/dl) (mg/dl) (mg/dl) (mg/dl) (mg/dl)
1 Group I 148± 1.58 112.0±51.58 61.0 ±1.58 88± .42 22 ±1.47
(control)
2 Group II 232.40±40.48 361.0± 1.58 38.0 ±1.58 161±1.69 72.15±1.58
(Butter Induced)
3 Group III ** *** *** ** **
(plant extract) 192.90±1.58 195.0± 1.58 42± 1.58 106±1.78 33.0±1.58
4 Group IV *** *** *** *** ***
(standard Lovastatin) 149.20± 1.92 164.52±1.58 37.58±1.31 123± .58 39 ±1.53
Values are expressed as mean ± SEM. Levels of significance- Group II compared with Group I,III and IV. **p 0.01 and ***p 0.001.

125
Asian J. Res. Pharm. Sci. 2011; Vol. 1: Issue 4, Pg 124-127 [AJPSci.]

DISCUSSION: decrease in oxidative stress and protection of LDL from


Hyperlipidemia continues to be a health major problem in oxidation might therefore be a strategy with great promise
India and other developing countries, which lead to for prevention of atherosclerosis associated cardiovascular
important risk factors like atherosclerosis, stroke etc. disease (Steinbreg and Gotto, 1999). The intense interest
Hyperlipidemia evokes the damages in various tissue, in this area stems in part from the generally low toxicity of
which in turn, deregulates the cellular functions leading to antioxidants and the hope that treatment with antioxidants
damage to various pathological conditions (Chander et might be additive with cholesterol lowering regimes.
al.,2003).
VLDL particles are smaller than the chylomicrons and also
The present studies were performed to assess the are rich triglycerides though to a lesser extent VLDL
hypolipidemic activity and to prove its claim in folklore particles sizes vary widely ,with a concomitant variation of
practice against various disorders. Probucol, a the chemical composition ;the larger particles are rich in
hypolipidemic drug is a potent lipophilic antioxidant and triglycerides and in apo-c and the smaller particles depleted
the ability to inhibit atherosclerosis has been attributed to its of TG andsurface materials result from the hydrolysis of
antioxidant properties (Balakrishnan et al., 2006). Probucol VLDL by lipoprotein lipase activity. VLDL is the main
lowers the level of cholesterol in the bloodstream by carrier if triglycerides and it is less harmful than but still
increasing the rate of LDL catabolism. Additionally, can damage the arterial lining .
probucol may inhibit cholesterol synthesis and delay
cholesterol absorption. Probucol is a powerful antioxidant, VLDL production is directly related to the body fat
which inhibits the oxidation of cholesterol in LDLs, this (Kesavalu et al., 2001).Severe elevation in the VLDL
slows the formation of foam cells, which contribute to cholesterol lead to hypercholesterolemia Triglycerides are
atherosclerotic plaques. Similarly, flavonoids present in the mainly stored in the adipose tissue .The plasma lipoproteins
plant Mimosa pudica may be responsible for its are major sources of fatty acid to synthesis triacylglycerols.
hypolipidemic action and as already reported significant The excess of fat diet increased the TG level which is one
antioxidant activity of chloroform extract further confirms of the causes of hardening of arteries (XU et al., 2005).
its significant hypolipidemic activity .
CONCLUSION:
Cholesterol is synthesized in all animal tissue. It’s In accordance with these results it may be confirmed that
important relates to its role in the stabilization of membrane due to the presence of phytoconstituents such as flavonoids,
structures because of its rigid planar structure.It also as a alkaloids and glycosides in the ethanol extract, it could be
precursor for the synthesis of steroid hormones . Increased responsible for the observed significant hypolipidemic
amount of cholesterol leads to cardiovascular disease activity. In conclusion,it can be said that the ethanol extract
particularly coronary heart disease (CHD) (Aparna et al., of Mimosa pudica exhibited a significant hypolipidemic
2003). activity.

The plasma cholesterol was reduced remarkably on treating REFERENCES:


the HFD mice with ethanol extract of Mimosa pudica 1. Adikari NS. Prevention of disease through cure, yojana, 36( 1-
Linn.The lipid lowering effects may be due to the presence 3); 2003: 42-44.
of plant sterol. Plant sterol reduces the absorption of 2. Ahire AE and Laddha KS. Hypolipidemic effects of Carthamus
tinctorius in rats. Indian Drugs. 42(8): 2005: 545-546.
cholesterol and thus increases the fecal excretion of steroids 3. Alexander RW. Hypertension and pathogenesis of
that results in decrease of body lipids atherosclerosis- oxidative stress and mediation of arterial
Reduction 1% cholesterol produces a 2% to 3% reduction in inflammatory response – A new perspective. Hypertension 25:
coronary heart disease risk (Ornish et al., 1985). 1995;155-161.
4. Aparna Berteri R. Risk of coronary artery heart disease, Health
screen 1; 2003:28-29.
Triglycerides are mainly stored in the adipose tissue
5. Balakrishnan N, Suresh D, Pandian GS, Edwin E and Sheeja E.
(Ahire,2005). The plasma lipoproteins are major sources of Anti-diarrhoeal potential of Mimosa pudica root extracts. Indian
fatty acid to synthesis triacylglycerols. The excess of fat J Nat Prod 22(2): 2006; 21-23.
diet increased the TG level which is one of the causes of 6. Blackwelder WD . The cause of complication of DM Indian
hardening of arteries (XU et al., 2005). Journal of Experimental Biology 25; 1977: 490.
HDL is known as the good cholesterol it has reversed the 7. Chander R, Kapoorn K and Singh C. Lipid per oxidation of
hyperlipidemic rat serum in chronic ethanol and acetaldehyde
transport function. It carries cholesterol away from the admimistration J Biosciences 13; 2003:289-274.
including the coronary categories and drops it off at the 8. Chattopadhyaya R, Pathak D and Jindal DP. Indian Drugs 33:
liver (Ginsberg and Annapurna,2004). 1996; 85-97.
9. Ghani A. Medicinal plants of Bangladesh with chemical
HDL is directly anti- androgenic and it is belived to remove constituents and uses. 1998. Dhaka: Asiatic society of
Bangladesh; 2nd ed.
cholesterol from the developing lesions (Sonnerberg et al., 10. Ginsberg H and Annapurna N.A Lipoprotein physiology in non
1993). diabetic and diabetic status relation to atherogenesis. J debetic
LDL is a risk factor and plays a role at several steps of care 2004: 839-855.
atherosclerosis (Witzum, 1994; Alexander, 1995). A

126
Asian J. Res. Pharm. Sci. 2011; Vol. 1: Issue 4, Pg 124-127 [AJPSci.]

11. Harborne JB. Phytochemical methods: a guide to modern


technique of plant analysis. 1984: NewYork: Chapman and Hall;
2nd ed.
12. Kesavulu M, Kemeshwara M, Rao B and Giri R. lipid
peroxidation and antioxodent enzyme status in type to diabetics
with coronary heart disease , Diab Res and Clin Prac., 1(53);
2001: 33-39.
13. Ornish D and Rosner B . The effect of intake of dietary fat
JAMA . 49; 2005: 263-267.
14. Rajendran R, Hemachander R, Ezhilarasan T, Keerthana C,
Saroja DL and Saichand KV. Phytochemical analysis and in-vitro
antioxidant activity of Mimosa pudica Linn leaves. Research J.
Pharm and Tech 3(2): 2010;551-555.
15. Sonnerberg and Zolber L. Risk of coronary artery heart disease,
American Dietic Association chircago.2009.
16. Steinberg D and Gotto AM. Preventing coronary artery disease
by lowering cholesterol levels- Fifty years from bench to bedside.
JAMA 282(21): 1999; 43-50.
17. Witzum JL. The oxidation hypothesis of atherosclerosis. Lancet
344(8925): 1994;793-795.
18. Xu Y, He Z and King GL. Introduction of hyperglycemia and
dyslipidemia in the pathogenesis of diabetic vascular
complications. Curr Diab Rep 5(2); 2005: 91-97.

127

You might also like

pFad - Phonifier reborn

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy