Green tea extract attenuates hepatic steatosis by decreasing adipose lipogenesis and enhancing hepatic antioxidant defenses in ob/ob mice

作者: Hea Jin Park , Dana A. DiNatale , Min-Yu Chung , Young-Ki Park , Ji-Young Lee

DOI: 10.1016/J.JNUTBIO.2010.03.009

关键词:

摘要: Excess hepatic lipid accumulation and oxidative stress contribute to nonalcoholic fatty liver disease (NAFLD). Thus, we hypothesized that the hypolipidemic antioxidant activities of green tea extract (GTE) would attenuate events leading NAFLD. Obese mice (ob/ob; 5 weeks old, n=38) their lean littermates (n=12) were fed 0%, 0.5% or 1% GTE for 6 weeks. Then, steatosis, inflammatory markers measured. mice, compared controls, had greater lipids serum alanine aminotransferase (ALT). at lowered (P<.05) ALT in obese mice. The GTE-mediated attenuation steatosis was accompanied by decreased mRNA expression adipose sterol regulatory element-binding protein-1c, acid synthase, stearoyl CoA desaturase-1, hormone-sensitive lipase nonesterified concentrations. Immunohistochemical data indicated steatotic livers from extensive tumor necrosis factor-α (TNF-α), whereas TNF-α protein inhibited expression. Hepatic total glutathione, malondialdehyde Mn- Cu/Zn-superoxide dismutase normalized levels littermates. Also, increased catalase glutathione peroxidase activities, these inversely correlated with lipids. Collectively, mitigated NAFLD injury ob/ob decreasing release acids inhibiting peroxidation as well restoring defenses responses. These findings suggest may be used an effective dietary strategy mitigate obesity-triggered

参考文章(52)
Philip C Chen, Derek S Wheeler, Vivek Malhotra, Kelli Odoms, Alvin G Denenberg, Hector R Wong, None, A green tea-derived polyphenol, epigallocatechin-3-gallate, inhibits IκB kinase activation and IL-8 gene expression in respiratory epithelium Inflammation. ,vol. 26, pp. 233- 241 ,(2002) , 10.1023/A:1019718718977
Joshua D. Lambert, Shengmin Sang, Chung S. Yang, Biotransformation of Green Tea Polyphenols and the Biological Activities of Those Metabolites Molecular Pharmaceutics. ,vol. 4, pp. 819- 825 ,(2007) , 10.1021/MP700075M
S. M. Turner, S. Roy, H. S. Sul, R. A. Neese, E. J. Murphy, W. Samandi, D. J. Roohk, M. K. Hellerstein, Dissociation between adipose tissue fluxes and lipogenic gene expression in ob/ob mice. American Journal of Physiology-endocrinology and Metabolism. ,vol. 292, ,(2007) , 10.1152/AJPENDO.00309.2005
Jing Zhao, Hui Chen, Yan Li, Protective effect of bicyclol on acute alcohol-induced liver injury in mice. European Journal of Pharmacology. ,vol. 586, pp. 322- 331 ,(2008) , 10.1016/J.EJPHAR.2008.02.059
Claudia P. M. S. de Oliveira, Vicência M. R. de Lima, Fernanda I. Simplicio, Francisco G. Soriano, Evandro S. de Mello, Heraldo P. de Souza, Venâncio A. F. Alves, Francisco R. M. Laurindo, Flair J. Carrilho, Marcelo G. de Oliveira, Prevention and reversion of nonalcoholic steatohepatitis in OB/OB mice by S-nitroso-N-acetylcysteine treatment. Journal of The American College of Nutrition. ,vol. 27, pp. 299- 305 ,(2008) , 10.1080/07315724.2008.10719703
Yoko Shishikura, Santosh Khokhar, Brent S. Murray, Effects of tea polyphenols on emulsification of olive oil in a small intestine model system. Journal of Agricultural and Food Chemistry. ,vol. 54, pp. 1906- 1913 ,(2006) , 10.1021/JF051988P
A DIEHL, Lessons from animal models of NASH Hepatology Research. ,vol. 33, pp. 138- 144 ,(2005) , 10.1016/J.HEPRES.2005.09.022
J.A. Escobar, M.A. Rubio, E.A. Lissi, SOD and catalase inactivation by singlet oxygen and peroxyl radicals Free Radical Biology and Medicine. ,vol. 20, pp. 285- 290 ,(1996) , 10.1016/0891-5849(95)02037-3