Anti-obesity and Antihyperlipidemic Activity of Ougeinia oojeinensis (Roxb.) in High Fat Diet-Induced Obesity in Experimental Animals
DOI:
https://doi.org/10.18311/jnr/2023/32197Keywords:
Antihyperlipidemic Anti-Obesity, Antioxidant, Lipid Profile, O. oojeinensisAbstract
The present study was planned to assess the anti-obesity efficacy of petroleum ether, ethyl acetate, and methanolic extracts of leaves of Ougeinia oojeinensis (Roxb.) belonging to the family Fabaceae. The soxhlation method was employed to produce the extracts. Wistar rats were subjected to a high-fat diet for 40 days to induce obesity. Along with the high-fat diet, a standard drug Orlistat 50 mg/kg and various extracts of O. oojeinensis at 100 mg/kg and 200 mg/kg were administered for 40 days. The key markers like lipid profiles, SGOT, SGPT, glucose, body weight, food intake, body temperature, atherogenic index, coronary index, and weight of the organs were assessed. The anti-antioxidant properties like TBARS, GSH, GR, Gpx, SOD, and CAT were also estimated. The results revealed that O. oojeinensis with the doses 100 and 200 mg/kg showed significant Anti obese and hypolipidemic effects in rats fed with a high-fat diet.
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Copyright (c) 2023 K. Jagadeeshwar, R. Subhakara Raju, G. Chakravarthi, A. Rajasekhar Reddy, G. S. N. Koteswara Rao, Narender Malothu (Author)
This work is licensed under a Creative Commons Attribution 4.0 International License.
Accepted 2023-04-24
Published 2023-06-13
References
Obesity and overweight [Internet]. 2021. Available from: https://www.who.int/news-room/fact-sheets/ detail/obesity-and-overweight
Zhao C, Castonguay TW. Effects of free access to sugar solutions on the control of energy intake, Food Rev Int. 2017; 33(2):105-22. https://doi.org/10.1080/87559129.2016.1149863 DOI: https://doi.org/10.1080/87559129.2016.1149863
Withrow D, Alter D. The economic burden of obesity worldwide: a systematic review of the direct costs of obesity. Obes Rev 2011; 12(2):131-41. https://doi.org/10.1111/j.1467-789X.2009.00712.x DOI: https://doi.org/10.1111/j.1467-789X.2009.00712.x
Naja F, Hwalla N, Itani L, Karam S, Sibai AM, Nasreddine L. A Western dietary pattern is associated with overweight and obesity in a national sample of Lebanese adolescents (13-19 years): a cross-sectional study. Br J Nutr. 2015; 114(11):1909-19. https://doi.org/10.1017/S0007114515003657 DOI: https://doi.org/10.1017/S0007114515003657
Niemann B, Rohrbach S, Miller M, Newby D, Fuster V and Kovacic J. Oxidative stress and cardiovascular risk: obesity, diabetes, smoking, and pollution: Part 3 of a 3-Part Series. J Am Coll Cardiol. 2017; 70(2):230- 51. https://doi.org/10.1016/j.jacc.2017.05.043 DOI: https://doi.org/10.1016/j.jacc.2017.05.043
Khare CP. Indian herbal remedies. Rational western therapy, ayurvedic and other traditional usage, Botany. 2014.
Sahu R, Dewangan D, Roy A and Namdev K. Antiinflammatory action of O. oojeinensis (Roxb.) Hochr. Bark by HRBC membrane stabilization. Res J Pharm Technol. 2008; 1(1):57-8.
Samyal ML, Ahmed Z, Bhushan S. Overview of O. oojeinensis: Medicinal Plant. J Chem Pharm Sci. 2013; 6(2):73-7.
Patwardhan S, Vadnal P, Kumar Singhai A, Somani R. Studies of hepatoprotective activity of ethanolic extract of Cassia fistula bark against CCL4 induced hepatic damage in Wistar rats. Pharmacologyonline. 2009; 2:50-63.
Woods S, Seeley R, Rushing P, D’Alessio D, Tso P. A controlled high-fat diet induces an obese syndrome in rats. The J Nutr. 2003; 133(4):1081-7. https://doi.org/10.1093/jn/133.4.1081 DOI: https://doi.org/10.1093/jn/133.4.1081
Jagadeeshwar K, Kulandaivelu U, GsnK Rao, Alavala RR, Panda SP. Evaluation of lipid lowering activity and anti-oxidant status of pithecellobium dulce in obesity induced rats. Indian J Pharm Sci. 2020; 82(6):1067-71. https://doi.org/10.36468/pharmaceutical-sciences.742 DOI: https://doi.org/10.36468/pharmaceutical-sciences.742
Friedewald WT, Levey RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972; 18(6):499-502. https://doi.org/10.1093/clinchem/18.6.499 DOI: https://doi.org/10.1093/clinchem/18.6.499
Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95(2):351-8. https://doi.org/10.1016/0003-2697(79)90738-3 DOI: https://doi.org/10.1016/0003-2697(79)90738-3
Rotruck JT, Pope AL, Ganther HE, Swanson AB, Hafeman DG, Hoekstra WG. Selenium: Biochemical role as a component of glutathione peroxidase. Science. 1973; 179(4073):588-90. https://doi.org/10.1126/science.179.4073.588 DOI: https://doi.org/10.1126/science.179.4073.588
Bergmayer HU. Methods of enzymatic analysis. Verlag Chemie G.m.b.H., Weinheim/Bergstr. (Germany) and Academic Press, New York and London. Starch.1963; 15(7):237-74.
McGown MW, Artuss JD, Strandbergh DR, Zak B. A peroxidase-coupled method for the colorimetric determination of serum triglycerides. Clin Chem. 1983; 29(3):538-43. https://doi.org/10.1093/clinchem/29.3.538 DOI: https://doi.org/10.1093/clinchem/29.3.538
Charles AW, John FK. Methods of enzymatic analysis, Metabolites 1: Carbohydrates. Br Polym J. 1985; 17(4):379. https://doi.org/10.1016/0308-8146(85)90039-1 DOI: https://doi.org/10.1016/0308-8146(85)90039-1
Kakkar P, Das B, Viswanathan PN. A modified spectrophotometric assay of superoxide dismutase. Indian J Biochem Biophys. 1984; 21(2):130-2.
Sinha AK. Colorimetric assay of catalase. Anal Biochem. 1972; 47(2):389-94. https://doi.org/10.1016/0003-2697(72)90132-7 DOI: https://doi.org/10.1016/0003-2697(72)90132-7
Eidi A, Eidi M, Esmaeili E. Antidiabetic effect of garlic (Allium sativum L.) in normal and streptozotocin- induced diabetic rats. Phytomedicine. 2006; 13(9-10):624-9. https://doi.org/10.1016/j.phymed. 2005.09.010 DOI: https://doi.org/10.1016/j.phymed.2005.09.010
Bais S, Singh GS, Sharma R. Antiobesity and hypolipidemic activity of Moringa oleifera leaves against high fat diet-induced obesity in rats. Adv Biol. 2014; 1-9. https://doi.org/10.1155/2014/162914 DOI: https://doi.org/10.1155/2014/162914
Abbott RD, Wilson PW, Kannel WB, Castelli WP. High density lipoprotein cholesterol, total cholesterol screening, and myocardial infarction. The Framingham Study. Arteriosclerosis. 1988; 8(3):207- 11. https://doi.org/10.1161/01.ATV.8.3.207 DOI: https://doi.org/10.1161/01.ATV.8.3.207
Aune D, Sbhijit S, Sabrina S, Teresa N, Imre J, Romundastad P, et al. Body mass index, abdominal fatness, fat mass and the risk of atrial fibrillation: a systematic review and dose-response meta-analysis of prospective studies. Eur J Epidemiol. 2017; 32(3):181- 92. https://doi.org/10.1007/s10654-017-0232-4 DOI: https://doi.org/10.1007/s10654-017-0232-4
Hariri N, Thibault L. High-fat diet-induced obesity in animal models. Nutr Res Rev. 2010; 23(2):270-99. https://doi.org/10.1017/S0954422410000168 DOI: https://doi.org/10.1017/S0954422410000168
Sjostrom L. Review of the key results from the Swedish Obese Subjects (SOS) trial - A prospective controlled intervention study of bariatric surgery. J Intern Med. 2013; 273(3):219-34. https://doi.org/10.1111/joim.12012 DOI: https://doi.org/10.1111/joim.12012
Kersten S. Mechanisms of nutritional and hormonal regulation of lipogenesis. EMBO Reports. 2001; 2(4):282-6. https://doi.org/10.1093/embo-reports/ kve071 DOI: https://doi.org/10.1093/embo-reports/kve071
Bederman IR, Steven F, Visvanathan C, James CA, Stephen FP. Triglyceride synthesis in epididymal adipose tissue. J Biol Chem. 2009; 284(10):6101-08. https://doi.org/10.1074/jbc.M808668200 DOI: https://doi.org/10.1074/jbc.M808668200
Parish S, Alison O, Robert C, Jemma CH, Michael RH, James DO, et al. Lipids and lipoproteins and risk of different vascular events in the mrc/bhf heart protection study. Circulation. 2012; 125(20):2469-78. https://doi.org/10.1161/CIRCULATIONAHA.111.073684 DOI: https://doi.org/10.1161/CIRCULATIONAHA.111.073684
Nakamura A, Terauchi Y. Lessons from mouse models of high-fat diet-induced NAFLD. Int J Mol Sci. 2013; 14; 21240-57. https://doi.org/10.3390/ijms141121240 DOI: https://doi.org/10.3390/ijms141121240
Mahluji S, Vahide EA, Majid M, Payahoo L, Alireza O, Samad EJG. Effects of ginger (Zingiber officinale) on plasma glucose level, HbA1c and insulin sensitivity in Type-2 diabetic patients. Int J Food Sci Nutr. 2013; 64(6):682-6. https://doi.org/10.3109/09637486. 2013.775223 DOI: https://doi.org/10.3109/09637486.2013.775223
David BA. Transaminases. FEBS Letters. 1985; 190:179-80. https://doi.org/10.1016/0014-5793(85) 80462-2 DOI: https://doi.org/10.1016/0014-5793(85)80462-2