Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Anti-Obesity Activity of Ethanolic Extract of Moringa oleifera Seeds in Experimental Animals


Affiliations
1 Department of Pharmacocology, Sree Siddaganga College of Pharmacy, Tumkur-572 102, India
     

   Subscribe/Renew Journal


Background and Objectives: Obesity is closely associated with life-style-related disorders such as arteriosclerosis, hyperlipidemia, hypertension and type-2 diabetes mellitus. Moringa oleifera Lam. Seeds were proved scientifically for the treatment of lifestyle related disorders. Present study was performed to clarify whether an M. oleifera Lam. Seeds ethanol extract (MOE) prevent high-fat diet-induced obesity in mice fed for nine weeks.

Methods: We have performed two in vivo experiments such as high-fat diet-induced obesity mice model and lipid emulsion tolerance test in normal rats. In high-fat diet-induced obesity mice model, female Swiss mice were fed a high fat diet (HFD; 40% fat) with or without 1 or 2 % of MOE or 0.012% orlistat for nine weeks. In lipid emulsion tolerance test male Wistar rats were orally administered, lipid emulsion with or without 500 mg/kg or 1000 mg/kg of MOE and the plasma triglycerides were measured from 0.5 to 5 h.

Results: Consumption of HFD containing MOE to mice for nine weeks exhibited significant reduction in lipid parameters, body weight, parametrial adipose tissue weight, liver TG and different organs weight compared to HFD fed control. Whereas, improvement in insulin resistance induced by HFD alone group. Furthermore, consumption of a HFD containing 1 or 2 % of MOE significantly increased the fecal content and fecal triglyceride compared with the HFD group. Pre-treatment with MOE inhibited the elevated plasma triglyceride level after the oral administration of the lipid emulsion to rats. In other words, administration of MOE improves lipid tolerance in rats.

Conclusion: Observed anti-obesity activity of MOE in experimental animals may be partly mediated through delaying the intestinal absorption of dietary fat by inhibiting pancreatic lipase activity as evident from similar profile of activity as that of orlistat.


Keywords

MOE, High Fat Diet, Insulin Tolerance, Lipid Parameter, Lipid Emulsion, Fecal TG.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Leonhardt M, Hrupka B, Langhans W. New approaches in the pharmacological treatment of obesity. Eur J Nutr. 38; 1999: 1-13.
  • Hill JO, Melanson EL, Wyatt HT. Dietary fat intake and regulation of energy balance: implications for obesity. J Nutr. 130; 2000: 284S-8S.
  • Leslie WS et al. Weight management: a comparison of existing dietary approaches in a work-site setting. Endocrine Rev. 26; 2002: 1469-75.
  • Verger R. Pancreatic lipase. Edited by: Borgstrom B, Brockman HL. Elsevier, Amsterdam, 1984: 83-105.
  • Bray and Greenway. Current and potential drugs for treatment of obesity. Endocrine Rev. 20; 1999: 805-75.
  • Sarah HB, Robert B, Clifford JB. High body mass index for age among US children and adolescents. Asian Nat Prod Res. 4; 2000: 321-7.
  • Guevara AP, Vargas C, Sakurai H, Fujiwara Y, Hashimoto K, Maoka T et al. An antitumor promoter from Moringa oleifera. Mutat Res. 440; 1999: 181-8.
  • Makkar PS and Becker K. Nutrients and anti-quality factors in different morphological parts of the Moringa oleifera tree. Journal of Agricultural Science. 128; 1997: 311-22.
  • Makkar HP and Becker K. Nutritional value and anti-nutritional components of whole and extracted Moringa oleifera leaves. Anim. Feed Sci. Technol. 63; 1996: 211-28.
  • Li-Kun H, Bao-Jun X, Yoshiyuki K, Yi-nan Z and Hiromichi O. Platycodi radix affects lipid metabolism in mice with high fat diet-induced obesity. J Nutr. 130; 2000: 2760-4.
  • Ukwuani AN, Abukakar MG, Shehu RA and Hassan LG. Anti obesity effects of pulp extract Tamarindus indica in albino rat. Asian Journal of Biochemistry. 3; 2008: 221-7.
  • Nair S, Feng, Machender RK, Xiaoping Y and Jun R. Chromium alleviate glucose intolerance, insulin resistance, and hepatic ER stress in obese mice. Obesity. 16; 2008: 1331-7.
  • Li-Kun H, Yi-Nan Z, Masayuki Y, Hiromichi O and Yoshiyuki K. Anti-obesity effects of chikusetsusaponins isolated from Panax japonicus rhizomes. BMC Complementary and Alternative Medicine. 5; 2005: 1-10.
  • Friedewald WT, Levy RI and Fredrickson DS. Estimation of low-density lipoprotein cholesterol in plasma, without use of the preparative centrifuge. Clinical Chemistry. 18; 1972: 499-501.
  • Wencong L, Yinan Z, Likun H, HaiminW, Masato S, Mingsong L et al. Saponins (Ginsenosides) from stems and leaves of Panax quinquefolium prevented high-fat diet-induced obesity in mice. Phytomedicine. 15; 2008: 1140–5.
  • Gurpreet K, Kulkarni SK. Antiobesity effect of a polyherbal formulation, ob-200g in female rats fed on cafeteria and atherogenic diets. Indian Journal of Pharmacology. 32; 2000: 294-9.
  • Mingfang L and Bernard MY. Pharmacotherapy for obesity. Br J Clin Pharmacol. 6; 2007: 804-10.
  • Faizi S, Siddiqui BS, Saleem R, Siddiqui S, Aftab K, Gilani AH. Fully acetylated carbamate and hypotensive thiocarbamate glycosides from Moringa oleifera. Phytochemistry. 38; 1998: 957-63.
  • Lalas S, Tsaknis J. Extraction and identification of natural antioxidants from the seeds of Moringa oleifera tree variety of Malavi. J Am Oil Chem Soc. 79; 2002: 677-83.
  • Randle et al. The glucose fatty-acid cycle: Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. Lancet. 1; 1963: 785-9.
  • Belfiore F. Insulin resistance in obesity: Metabolic mechanisms and measurement methods. Mol Gen Metab. 65; 1998: 121-8.
  • 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. 26; 2004: 327-33.
  • Shafrir E et al. Contribution to the understanding of diabetes by study of its etiopathology in animal models. Diabetes Mellitus. 5; 2003: 231-55.
  • Newsholme, EA and Crabtree B. Biochem. Soc. Symp. 41; 1976: 61-110.
  • Kalopissis et al. Very-low-density-lipoprotein secretion by isolated hepatocytes of fat-fed rats. Biochem J. 198; 1981: 373-7.
  • Sambaiah MR and Satyanarayana MN. J Biosci. 12; 1987: 143.
  • Montani et al. Ectopic fat storage in key cardiovascular organs. Int J Biochem Cell Biol. 35; 2003: 807-25.

Abstract Views: 368

PDF Views: 2




  • Anti-Obesity Activity of Ethanolic Extract of Moringa oleifera Seeds in Experimental Animals

Abstract Views: 368  |  PDF Views: 2

Authors

B. Manjula
Department of Pharmacocology, Sree Siddaganga College of Pharmacy, Tumkur-572 102, India
Rayappa Hunasagi
Department of Pharmacocology, Sree Siddaganga College of Pharmacy, Tumkur-572 102, India
K. P. Shivalinge Gowda
Department of Pharmacocology, Sree Siddaganga College of Pharmacy, Tumkur-572 102, India

Abstract


Background and Objectives: Obesity is closely associated with life-style-related disorders such as arteriosclerosis, hyperlipidemia, hypertension and type-2 diabetes mellitus. Moringa oleifera Lam. Seeds were proved scientifically for the treatment of lifestyle related disorders. Present study was performed to clarify whether an M. oleifera Lam. Seeds ethanol extract (MOE) prevent high-fat diet-induced obesity in mice fed for nine weeks.

Methods: We have performed two in vivo experiments such as high-fat diet-induced obesity mice model and lipid emulsion tolerance test in normal rats. In high-fat diet-induced obesity mice model, female Swiss mice were fed a high fat diet (HFD; 40% fat) with or without 1 or 2 % of MOE or 0.012% orlistat for nine weeks. In lipid emulsion tolerance test male Wistar rats were orally administered, lipid emulsion with or without 500 mg/kg or 1000 mg/kg of MOE and the plasma triglycerides were measured from 0.5 to 5 h.

Results: Consumption of HFD containing MOE to mice for nine weeks exhibited significant reduction in lipid parameters, body weight, parametrial adipose tissue weight, liver TG and different organs weight compared to HFD fed control. Whereas, improvement in insulin resistance induced by HFD alone group. Furthermore, consumption of a HFD containing 1 or 2 % of MOE significantly increased the fecal content and fecal triglyceride compared with the HFD group. Pre-treatment with MOE inhibited the elevated plasma triglyceride level after the oral administration of the lipid emulsion to rats. In other words, administration of MOE improves lipid tolerance in rats.

Conclusion: Observed anti-obesity activity of MOE in experimental animals may be partly mediated through delaying the intestinal absorption of dietary fat by inhibiting pancreatic lipase activity as evident from similar profile of activity as that of orlistat.


Keywords


MOE, High Fat Diet, Insulin Tolerance, Lipid Parameter, Lipid Emulsion, Fecal TG.

References