Antiobesity activity of aqueous and ethanol extracts of Enicostemma littorale in high fat diet induced obese rats

Authors

  • Ankur garg Department of Pharmacology, M.M. College of Pharmacy, M.M. University, Mullana, Ambala, (Haryana), INDIA.
  • Dr Randhir Singh Department of Pharmacology, M.M. College of Pharmacy, M.M. University, Mullana, Ambala, (Haryana), INDIA India

Keywords:

Herbal treatment, lipase inhibitor, Obesity, Oxidative Stress, Orlistat

Abstract

Obesity is a chronic disorder of global prevalence and associated with morbidity and mortality. Therefore, attention is being focused on the investigation of plant-based drugs used in the traditional medicine for the treatment of obesity. The presents work evaluates the anti-lipase and antiobesity activity of ethanol and aqueous extracts of Enicostemma littorale (ElEe & ElAe) (Genitanaceae) (Synonym – Enicostemma axillare) in HFD induced obesity in rats. Male Wistar rats weighing 150-200 g were divided into different group’s i.e. Normal control, HFD control, Orlistat (lipase inhibitor), ElEe & ElAe at doses of 200, 400, 250 and 500 mg/kg p.o. Treatment was started after 6 weeks upto 12 weeks alongwith HFD (except normal control). Oxidative stress was measured by measuring MDA, SOD and GSH level. Obesity was assessed by measuring morphological parameters, serum glucose, serum cholesterol, triglycerides and HDL level. ElEe & ElAe at 200, 400, 250 and 500 mg/kg/orally significantly attenuated morphological parameters i.e. weight gain, BMI, WHR, obesity index and adiposity index respectively as compare to HFD control group. Similarly, serum glucose, triglyceride, total cholesterol and oxidative stress were found to be attenuated as compare to HFD control group. The aqueous and ethanol extracts of Enicostemma littorale exhibit significant anti-lipase and antiobesity activity in high fat diet induced obesity in rats.

References

Bays H, Blonde L, Rosenson R. Adiposopathy: how do diet, exercise and weight loss drug therapies improve metabolic disease in overweight patients. Expert Review of Cardiovascular Therapy. 2006; 4: 871-895.

Reeves AF, Rees JM, Schiff M, Hujoel P. Total body weight and waist circumference associated with chronic periodontitis among adolescents in the United States. Archives of Pediatrics & Adolescent Medicine. 2006; 160: 894-899.

Jeffcoat R. Obesity - A perspective based on the biochemical interrelationship of lipids and carbohydrates. Medical Hypotheses. 2007; 68: 1159-71.

World Health Organization. Obesity: preventing and managing the global epidemic. Report of a WHO Consultation on obesity, WHO/NUT/NCD/98, Geneva, Switzerland, 1998): 1–275.

Wu CH, Yang MY, Chan KC, Chung PJ, Ou TT, Wang CJ. Improvement in high-fat diet-induced obesity and body fat accumulation by a Nelumbo nucifera leaf flavonoid-rich extract in mice. J. Agric. Food Chem. 2010; 58: 7075-7081.

Leelaprakash G, Mohan Dass S. Antimicrobial activity and phytochemical screening of methanol extract of Enicostemma axillare. Int J Pharm Pharm Sci. 2012; 4: 342-348.

Ja R, Thakar KA. “Chemical investigation of Enicostemma littorale Blume.” Current Science. 1966; 35: 145-160.

Ghosal S, Sharma PV, Chaudhuri RK.“Chemical constituents of gentianaceae X: xanthone O glucosides of Swertia purpurascensWall.” J of Pharmaceutical Scie. 1974; 63: 1286-1290.

Rama V, Clarina T, Maheswari M, Mabel GD. Pharmocognosy and Phytochemical study of Enicostemma Littorale Blume. Ameri J PharmTech Research. 2012; 2: 599-604.

Leelaprakash G, Mohan Dass S. In-vitro anti-inflammatory activity of methanol extract of Enicostemma axillare. Int J Drug Dev Res. 2011; 3: 189-196.

Soni S, Gupta S. In vitro anti plasmodial activity of Enicostemma littorale. Ame. J. Infectious Dis. 2009; 5: 259-262.

Praveena P, Sudarsanam D. In vitro antimicrobial activity studies on Enicostemma littorale (Lam), Raynal Whole plants. Int J Curr Res. 2011; 11: 123-124.

Garad MC, Upadhya MA, Kokare DM, Itankar PR. Aerial parts of Enicostemma littorale Blume serve as antipyretic and antacid: in vivo and in vitro evaluations. Pharmacogn Commun. 2012; 2: 42-45.

Kavimani S, Mani Senthil, Kumar KT. Effect of methanolic extract of Enicostemma littorale on Dalton’s ascetic lymphoma. J. Ethnopharmacol. 2000; 71: 349.

Vidyadhar S, Saidulu M, Gopal TK, Chamundeeshwari D, Umamaheshwarirao, David Banji. In vitro antihelmintic activity of the whole plant of Enicostemma littorale by using various extracts. Intl. J. Applied Biol. and Pharmaceutical Technol. 2010; 1: 1119-1125.

Kumar RS, Lakshmi PTV, Annamalai A. Effect of drying treatment on the content of antioxidants in Enicostemma littorale Blume. Research Journal of Medicinal plant. 2009; 3: 93-101.

Jaishree V, Badami S, Krishnamurthy PT. Antioxidant effect and hepatoprotective effect of ethyl acetate extract of Enicostemma axillare (Lam) Raynal against CCl4 induced liver injury in rats. Ind J Exp Bio. 2010; 48: 896-904.

Srinivasan K, Viswanad B, Asrat L, Kaul CL, Ramarao P. Combination of high-fat diet-fed and low-dose streptozotocin-treated rat: A model for type 2 diabetes and pharmacological screening. Pharmacol. Res. 2005; 52: 313-320.

Novellie LB, Diniz YS, Galhardi CM, Ebaid GMX, Rodrigues HG, Mani F, Fernandes AAH, Cicogna AC, Novelli JL, filho VB. Anthropometrical parameters and markers of obesity in rats. Lab. Animals. 2007; 41: 111-119.

Singh R, Krishan P. Modulation of impact of high fat diet in pathological and physiological left ventricular cardiac hypertrophy by fluvastatin. Biomed Pharmacother. 2010; 64: 147-53.

Kaushal, R, K.R. Dave S.S, Katyare. Paracetamol hepatotoxicity and microsomal function. Environ. Toxicol. Pharmacol. 1999; 1: 67-74.

Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95: 351-64.

Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Euro J Biochem. 1974; 47: 469-474.

Tietez F. Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues. Anal Biochem. 1969; 27: 502-502.

Woods SC, Seeley RJ, Rushing PA, D'Alessio D, Tso PA. Controlled high-fat diet induces an obese syndrome in rats. J Nutr. 2003; 133: 1081-87.

Storlien LH, James DE, Burleigh KM, Chisholm DJ, Kraegen EW. Fat feeding causes widespread in-vivo insulin resistance, decreased energy expenditure and obesity in the rat. Am J Physiol. 1986; 251: 576-583.

Woods SC, Seeley RJ. Understanding the physiology of obesity: review of recent developments in obesity research. Intl J Obes. 2002; 26: 8-10.

Rolls BJ, Hammer VA. Fat, carbohydrate and the regulation of energy intake. Amer J Clin Nutr. 1995; 62: 1086-1095.

Storlien LH, Jenkins AB, Chisholm DJ, Pascoe WS, Khouri S, Kraegen EW. Influence of dietary fat composition on development of insulin resistance in rats. Relationship to muscle triglyceride and omega-3 fatty acids in muscle phospholipid. Diabetes. 1991; 40: 280-89.

Van Itallie T.B, Health implications of overweight and obesity in the United States. Ann lnter Med. 1985; 103: 983-988.

Rosenson RS, Shott S, Tangney CC. Hypertriglyceridemia is associated with an elevated blood viscosity Rosenson: triglycerides and blood viscosity. Atherosclerosis. 2002; 161: 433-439.

Gluck FW, Kaufman SP, Walleck AS. Strategic management for competitive advantage. Harvard Business Review. 1980; 60: 154-161.

Ikemoto K, Satoh K, Maeda T, Fibiger HC. Neurochemical heterogeneity of the primate nucleus accumbens. Experimental Brain Research. 1995; 104: 177-190.

Oakes ND, Cooney GJ, Camilleri S, Chisholm DJ, Kraegen EW. Mechanisms of liver and muscle insulin resistance induced by chronic high-fat feeding. Diabetes. 1997; 46: 1768-1774.

Birari R.B, Bhutani K.K. Pancreatic lipase inhibitors from natural sources: Unexplored potential. Drug. Dis. Today. 2007; 12: 879-889.

Sharma N, Sharma V.K, Seo S.Y. Screening of some medicinal plants for anti-lipase activity. J. Ethnopharmacol. 2005; 97: 453-456.

Filippatos, T.D, Derdemezis C.S, Gazi I.F, Nakou E.S, Mikhailidis D.P, Elisaf M.S. Orlistat- associated adverse effects and drug interactions: a Critical review. Drug. Saf. 2008; 31: 53-65.

Han L.K, Kimura Y, Kawashima M, Takaku T, Taniyama T, Hayashi T, Zheng Y.N, H. Okuda. Anti-obesity effects in rodents of dietary teasaponin, a lipase inhibitor. Int. J. Obes. 2001; 25: 1459-1464.

Kwon C.S, Sohn H.Y, Kim S.H, Son K.H, Lee J.S, Lim J.K, Kim J.S. Anti-obesity effects of Dioscorea nipponica Makino with lipase inhibitory activity in rodents. Biosci. Biotechnol. Biochem. 2003; 1451-1456.

Ramgopal M, Attitalla A.H, Avinash P, Balaji M. Evalution of anti-lipidemic and anti-obesity efficacy of Bauhinia purpurea bark extract on rats fed with high fat diet. Acad. J. Plant. Sci. 2010; 3: 104-107.

Venkateshwarlu E, Sharvana B.B.S, Arvind P, Reddy P.R, Dileep P, Mahathi K. Evaluation of Anti-Diabetic and Hypolipidemic Activity of Pseudarthria viscida (Whole Plant) in Streptozotocin-Nicotinamide Induced Type II Diabetic Rats. Global J of Pharmacol. 2013; 7: 192-197.

Srinivasan K, Patole PS, Kaul CL, Ramarao P. Reversal of glucose intolerance by pioglitazone in high-fat diet fed rats. Methods Find Exp Clin Pharmacol. 2004; 26: 327- 33.

Colca JR, Dailey CF, Palazuk BJ, Hillman RM, Dinh DM, Melchior GW. Pioglitazone hydrochloride inhibits cholesterol absorption and lowers plasma cholesterol concentrations in cholesterol fed rats. Diabetes. 1991; 40: 1669-74.

Shafrir E. Diabetes in animals: Contribution to the understanding of diabetes by study of its etiopathology in animal models. In: Porte D, Sherwin RS, Baron A, editors. Diabetes mellitus. NewYork: McGraw-Hill. 2003; 231-55.

Kelley DE, He J, Menshikova EV, Ritov VB. Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes. Diabetes. 2002; 51: 2944-2950.

Malnick SDH, Knobler H. The medical complications of obesity. Q J Med. 2006; 99: 565-579.

Hasty H.A, Gruen M.L, Terry E.S, Surmi B.K, Atkinson R.D, Gao L. “Effects of vitamin E on oxidative stress and atherosclerosis in an obese hyperlipidemic mouse model,” Journal of Nutr Biochem. 2007; 18: 127–33.

Memisogulları R, Bakan E, “Levels of ceruloplasmin, transferin, and lipid peroxidation in the serum of patients with type 2 diabetes mellitus,” J of Diabetes and its Compl. 2004; 18: 193–207.

Ohkawa H, Ohishi N, Yagi K. “Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction,” Anal Biochem. 1979; 95: 351-64.

Vincent H.K, Innes K.E, Vincent K.R. “Oxidative stress and potential interventions to reduce oxidative stress in overweight and obesity,” Diabetes Obesity and Met. 2007; 9:813–39.

Downloads

Published

30-09-2014

How to Cite

1.
Ankur garg, Dr Randhir Singh. Antiobesity activity of aqueous and ethanol extracts of Enicostemma littorale in high fat diet induced obese rats. ijp [Internet]. 2014 Sep. 30 [cited 2024 Sep. 28];6(3):433-4. Available from: https://ijp.arjournals.org/index.php/ijp/article/view/356

Issue

Section

Original Research Articles