Lipids in Health and Disease | |
Terminalia paniculata bark extract attenuates non-alcoholic fatty liver via down regulation of fatty acid synthase in high fat diet-fed obese rats | |
Balaji Meriga2  Damineni Surekha1  Banavathy S Kruthika1  Mopuri Ramgopal2  | |
[1] Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bangalore, India;Department of Biochemistry, Sri Venkateswara University, Tirupati 517502, AP, India | |
关键词: Histopathology; AMPK-1α; FAS; Malondialdehyde; Catalase; Superoxide dismutase; Liver lipid profile; High fat diet; | |
Others : 805281 DOI : 10.1186/1476-511X-13-58 |
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received in 2013-12-17, accepted in 2014-03-17, 发布年份 2014 | |
【 摘 要 】
Background
This study was performed to understand the possible therapeutic activity of Terminalia paniculata ethanolic extract (TPEE) on non alcoholic fatty liver in rats fed with high fat diet.
Methods
Thirty six SD rats were divided into 6 groups (n = 6): Normal control (NC), high fat diet (HFD), remaining four groups were fed on HFD along with different doses of TPEE (100,150 and 200 mg/kg b.wt) or orlistat, for ten weeks. Liver tissue was homogenized and analyzed for lipid profiles, activities of superoxide dismutase (SOD), catalase (CAT) and malondialdehyde (MDA) content. Further, the expression levels of FAS and AMPK-1α were also studied in addition to histopathology examination of liver tissue in all the groups.
Results
HFD significantly increased hepatic liver total cholesterol (TC), triglycerides (TG), free fatty acids (FFA) and MDA but decreased the activities of SOD and CAT which were subsequently reversed by supplementation with TPEE in a dose-dependent manner. In addition, TPEE administration significantly down regulated hepatic mRNA expression of FAS but up regulated AMPK-1α compared to HFD alone fed group. Furthermore, western blot analysis of FAS has clearly demonstrated decreased expression of FAS in HFD + TPEE (200 mg/kg b.wt) treated group when compared to HFD group at protein level.
Conclusions
Our biochemical studies on hepatic lipid profiles and antioxidant enzyme activities supported by histological and expression studies suggest a potential therapeutic role for TPEE in regulating obesity through FAS.
【 授权许可】
2014 Ramgopal et al.; licensee BioMed Central Ltd.
【 预 览 】
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Figure 1. | 51KB | Image | download |
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【 参考文献 】
- [1]Feng L-J, Chen-Huan Y, Ying K-J, Hua J, Dai X-Y: Hypolipidemic and antioxidant effects of total flavonoids of Perilla frutescens leaves in hyperlipidemia rats induced by high-fat diet. Food Res Int 2011, 44:404-409.
- [2]Niimi M, Keyamura Y, Nozako M, Koyama T, Kohashi M, Yasufuku R, Yoshikawa T, Fan J: Probucol inhibits the initiation of atherosclerosis in cholesterol-fed rabbits. Lipids Health Dis 2013, 12(166):1-8.
- [3]Ok E, Do G-M, Lim Y, Park JE, Park YJ, Kwon O: Pomegranate vinegar attenuates adiposity in obese rats through coordinated control of AMPK signaling in the liver and adipose tissue. Lipids Health Dis 2013, 12(163):1-8.
- [4]Adams LA, Angulo P: Recent concepts in non-alcoholic fatty liver disease. Diabet Med 2005, 22:1129-1133.
- [5]Gauthier M-S, Favier R, Lavoie J-M: Time course of the development of non-alcoholic hepatic steatosis in response to high fat diet-induced obesity in rats. British J Nut 2006, 95:273-281.
- [6]Bravo E, Palleschi S, Aspichueta P, Buque X, Rossi B, Cano A, Napolitano M, Ochoa B, Kathleen MB: High fat diet-induced non alcoholic fatty liver disease in rats is associated with hyperhomocysteinemia caused by down regulation of the transsulphuration pathway. Lipids Health Dis 2011, 10(60):1-6.
- [7]Alsheikh-Ali AA, Kuvin JT, Karas RH: Risk of adverse events with fibrates. Am J Cardiol 2004, 94:935-938.
- [8]Yun JW: Possible anti-obesity therapeutics from nature a review. Phytochemistry 2010, 71:1625-1641.
- [9]Vasudeva N, Yadav N, Sharma SK: Natural products: a safest approach for obesity. Chin J Integr Med 2012, 18(6):473-480.
- [10]Talwar S, Nandakumar K, Nayak PG: Anti-inflammatory activities of Terminalia paniculata bark extract against acute and chronic inflammation in rats. J Ethnopharmacol 2011, 134(2):323-328.
- [11]Nadkarni AK: Terminalia Paniculata Roxb. In Indian Materia Medica. 3rd edition. Edited by Nadkarni KM. Mumbai, India: Popular Prakashan; 1996:931.
- [12]Eesha BR, Mohanbabu Amberkar V, Meena Kumari K, Sarath babu Vijay M, Lalit M, Rajput R: Hepatoprotective activity of Terminalia paniculata against paracetamol induced hepatocellular damage in wistar rats. Asian Pac J Trop Med 2011, 4(6):466-469.
- [13]Subramaniam R, Aiyalu R, Manisenthikumar KT: Investigation of hyperglycemic, hyperlipidemic and antioxidant activity of aqueous extract of Terminalia paniculata bark in diabetic rats. Asian Pac J Trop Biomed 2012, 2(3):262-268.
- [14]Anonymous: The Wealth of India: Raw Material, Publication and Information Directorate. New Delhi: CSIR; 1992:345-346.
- [15]Agrawa S, Giriraj T, Kulkarni VN, Sharma A: Comparative study on the antioxidant activity of methanolic extracts of Terminalia paniculata and Madhuca longifolia. Free Radic Antioxid 2011, 1(4):62-68.
- [16]Angulo P: Non alcoholic fatty liver disease. N Engl J Med 2002, 346:1221-1231.
- [17]Yang SF, Tzang BS, Yang KT, Hsiao Y, Chang YY, Chan CH: Taurine alleviates dyslipidemia in hamsters fed a high fat/cholesterol diet. Food Chem 2010, 120:156-162.
- [18]Sung YY, Yoon T, Kim SJ, Yang W-K, Kim HK: Anti-obesity activity of Allium fistulosum L. extract by down-regulation of the expression of lipogenic genes in high fat diet induced obese rats. Mol Med Rep 2011, 4:431-435.
- [19]Evans P, Halliwell B: Micronutrients: Oxidabt/antioxidant satus. Br J Nutr 2001, 85:S67-S74.
- [20]Hotamisligil GS: Inflammation and metabolic disorders. Nature 2006, 444:860-867.
- [21]Shoelson SE, Herrero L, Naaz A: Obesity, inflammation and insulin resistance. Gastroenterology 2007, 132:2169-2180.
- [22]Berger JP: Role of PPARγ, transcriptional cofactors, and adiponectin in the regulation of nutrient metabolism, adipogenesis and insulin action: view from the chair. J Obes 2005, 29:S3-S4.
- [23]Tamori Y, Masugi J, Nishino N, Kasuga M: The role of RRARγ in maintenance of the characteristics of mature 3 T3-L1 adipocytes. Diabetes 2002, 51:2045-2055.
- [24]Folch J, Lees M, Sloane Stanly GH: A Simple method for the isolation and purification of total lipids from animal tissue. J Biol Chem 1957, 226(1):497-509.
- [25]Beyer WE, Fridovich: for superoxide dismutase activity: some large consequences of minor changes in conditions. Anal Biochem 1987, 161:559-566.
- [26]Aebi H: Catalase in vitro. Methods Enzymol 1984, 105:121-126.
- [27]Buege J, Aust SD, colowick Sp, Kaplan No: Microsomal Lipid Peroxidation. In Methods in Enzymology. New York: Acadomic press; 1978:302-311.