Epigallocatechin gallate attenuates fibrosis, oxidative stress, and inflammation in non-alcoholic fatty liver disease rat model through TGF/SMAD, PI3 K/Akt/FoxO1, and NF-kappa B pathways

被引:160
|
作者
Xiao, Jia [1 ]
Ho, Chi Tat [2 ]
Liong, Emily C. [2 ]
Nanji, Amin A. [3 ]
Leung, Tung Ming [2 ,4 ]
Lau, Thomas Yue Huen [5 ]
Fung, Man Lung [6 ,7 ]
Tipoe, George L. [2 ,7 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Adv Technol, Ctr Gene & Cell Engn, Shenzhen, Peoples R China
[2] Univ Hong Kong, Li Ka Shing Fac Med, Dept Anat, Hong Kong, Peoples R China
[3] Dalhousie Univ, Sch Med, Dept Pathol & Lab Med, Halifax, NS, Canada
[4] Mt Sinai Sch Med, Div Liver Dis, Dept Med, New York, NY USA
[5] Hong Kong Polytech Univ, Fac Hlth & Social Sci, Dept Hlth Technol & Informat, Hong Kong, Peoples R China
[6] Univ Hong Kong, Li Ka Shing Fac Med, Dept Physiol, Hong Kong, Peoples R China
[7] Univ Hong Kong, Li Ka Shing Fac Med, Res Ctr Heart, Hormone & Healthy Aging Ctr, Hong Kong, Peoples R China
关键词
EGCG; NAFLD; Fibrosis; Oxidative stress; Inflammation; GREEN TEA EXTRACT; HEPATIC STELLATE CELLS; NITRIC-OXIDE; (-)-EPIGALLOCATECHIN-3-GALLATE BLOCKS; ACTIVATION; POLYPHENOLS; STEATOHEPATITIS; INHIBITION; INDUCTION; MICE;
D O I
10.1007/s00394-013-0516-8
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
To investigate the protective mechanisms of an 85 % pure extract of (-) epigallocatechin gallate (EGCG) in the development of fibrosis, oxidative stress and inflammation in a recently developed dietary-induced animal model of non-alcoholic fatty liver disease (NAFLD). Female Sprague-Dawley rats were fed with either normal rat diet or high-fat diet for 8 weeks to develop NAFLD. For both treatments, rats were treated with or without EGCG (50 mg/kg, i.p. injection, 3 times per week). At the end, blood and liver tissue samples were obtained for histology, molecular, and biochemical analyses. Non-alcoholic fatty liver disease (NAFLD) rats showed significant amount of fatty infiltration, necrosis, fibrosis, and inflammation. This was accompanied by a significant expressional increase in markers for fibrosis, oxidative stress, and inflammation. TGF/SMAD, PI3 K/Akt/FoxO1, and NF-kappa B pathways were also activated. Treatment with EGCG improved hepatic histology (decreased number of fatty score, necrosis, and inflammatory foci), reduced liver injury (from similar to 0.5 to similar to 0.3 of ALT/AST ratio), attenuated hepatic changes including fibrosis (reduction in Sirius Red and synaptophysin-positive stain) with down-regulation in the expressions of key pathological oxidative (e.g. nitrotyrosine formation) and pro-inflammatory markers (e.g. iNOS, COX-2, and TNF-alpha). EGCG treatment also counteracted the activity of TGF/SMAD, PI3 K/Akt/FoxO1, and NF-kappa B pathways. Treatment with EGCG did not affect the healthy rats. Epigallocatechin gallate (EGCG) reduced the severity of liver injury in an experimental model of NAFLD associated with lower concentration of pro-fibrogenic, oxidative stress, and pro-inflammatory mediators partly through modulating the activities of TGF/SMAD, PI3 K/Akt/FoxO1, and NF-kappa B pathways. Therefore, green tea polyphenols and EGCG are useful supplements in the prevention of NAFLD.
引用
收藏
页码:187 / 199
页数:13
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