Astragaloside IV Attenuates Lipolysis and Improves Insulin Resistance Induced by TNFα in 3T3-L1 Adipocytes

被引:62
作者
Jiang, Boren [1 ,2 ]
Yang, Ying [1 ]
Jin, Hua [1 ]
Shang, Wenbin [1 ]
Zhou, Libin [1 ]
Qian, Lei [1 ]
Chen, Mingdao [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Inst Endocrine & Metab Dis, Ruijin Hosp,Shanghai Ctr Endocrine & Metab Dis, Sch Med,Dept Endocrine & Metab Dis, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Dept Endocrine & Metab Dis, Shanghai Peoples Hosp 9, Shanghai 200011, Peoples R China
关键词
astragaloside IV; 3T3-L1; adipocytes; MAPK; TNF alpha; lipolysis; perilipin;
D O I
10.1002/ptr.2434
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Increased circulating free fatty acid (FFA) concentrations have been demonstrated to potentially link obesity, insulin resistance and cardiovascular diseases. Astragaloside IV (AS-IV) is a saponin which is widely used in traditional Chinese medicine to treat type 2 diabetes and cardiovascular diseases. The purpose of the present study was to examine the effects of AS-IV on the lipolysis and insulin resistance induced by tumor necrosis factor-alpha (TNF alpha) in cultured 3T3-L1 adipocytes. TNFa promotes lipolysis in mammal adipocytes via the mitogen activated protein kinase (MAPK) family resulting in reduced expression/function of perilipin. Application of AS-IV inhibited TNF alpha-induced accelerated lipolysis in a dose-dependent manner, which was compatible with suppressed phosphorylation of ERK1/2 and reversed the downregulation of perilipin. Moreover, TNFa induced downregulation of key enzymes in lipogenesis, including LPL, FAS and GPAT, were also attenuated by AS-IV. Further studies showed that AS-IV improved TNFa-induced insulin resistance in 3T3-L1 adipocytes. This study provides the first direct evidence of the antilipolytic action of AS-IV in adipocytes, which may allow this agent to decrease the circulating FFA levels, thus increase insulin sensitivity and treat cardiovascular diseases. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:1434 / 1439
页数:6
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