Anti-inflammatory effect of genistein on non-alcoholic steatohepatitis rats induced by high fat diet and its potential mechanisms

被引:106
作者
Ji, Guiyuan [1 ]
Yang, Qinhe [2 ]
Hao, Jing [3 ]
Guo, Lina [4 ]
Chen, Xiang [1 ]
Hu, Jianping [1 ]
Leng, Liang [1 ]
Jiang, Zhuoqin [1 ]
机构
[1] Sun Yat Sen Univ, Sch Publ Hlth, Dept Nutr, Guangzhou 510080, Guangdong, Peoples R China
[2] Jinan Univ, Coll Med, Dept Tradit Chinese Med, Guangzhou 510632, Guangdong, Peoples R China
[3] Chinese Acad Sci, S China Bot Garden, Key Lab Plant Resources Conservat & Sustainable U, Guangzhou 510650, Guangdong, Peoples R China
[4] Guangdong Hosp Tradit Chinese Med, Dept Nutr, Guangzhou 510120, Guangdong, Peoples R China
关键词
Genistein; Non-alcoholic steatohepatitis; High fat diet; Tumor necrosis factor alpha; Nuclear factor kappa B; c-Jun N-terminal kinase; NF-KAPPA-B; LIVER-DISEASE; OXIDATIVE STRESS; PROTEIN-KINASES; ACTIVATION; ISOFLAVONES; LIPOPOLYSACCHARIDE; INDUCTION; PATHWAYS; CASCADES;
D O I
10.1016/j.intimp.2011.01.036
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Genistein is a naturally occurring plant-derived phytoestrogen present in the human diet, and is known to possess anti-cancer, anti-oxidant and anti-osteoporosis effects. Anti-inflammatory activity of genistein has been revealed in animal studies. In this paper, we investigated the anti-inflammatory effect of genistein on non-alcoholic steatohepatitis (NASH) rats induced by high fat diet (HFD), and explored its potential mechanisms. Rats were fed with normal chow diet or HFD for 12 weeks with or without low (4 mg/kg/day body weight) or high (8 mg/kg/day body weight) dose of genistein. Serum levels of aminotransferases, thiobarbituric acid-reactive substances (TBARS), tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6) and transforming growth factor beta (TGF-beta(1)) were measured, hepatic inflammation, liver TBARS, IL-6, TNF-alpha and TGF-beta(1) levels were determined, and proteins involved in mitogen-activated protein kinases (MAPKs) and nuclear factor-kappa B (NF-kappa B) pathways were assayed. The results showed that the NASH model rats reproduced typical pathogenetic and histopathological features of NASH in human, and genistein administration improved liver function, slowed down NASH progression, decreased the levels of TBARS, TNF-alpha and IL-6 in serum and liver, as well as inhibited I kappa B-alpha phosphorylation, nuclear translocation of NF-kappa B p65 subunit, and activation of c-Jun N-terminal kinase (JNK). In conclusion, genistein may be a promising drug to inhibit the inflammatory process and prevent liver damage in patients with NASH. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:762 / 768
页数:7
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