Promotion of adiponectin multimerization by emodin: A novel AMPK activator with PPARγ-agonist activity

被引:76
作者
Chen, Zhifen [1 ]
Zhang, Lu [1 ]
Yi, Junyang [1 ]
Yang, Zhuanbo [1 ]
Zhang, Zhijie [2 ]
Li, Zhen [1 ]
机构
[1] Tsinghua Univ, Sch Life Sci, MOE Key Lab Bioinformat, Beijing 100084, Peoples R China
[2] China Acad Chinese Med Sci, Inst Chinese Mat Med, Beijing 100700, Peoples R China
基金
美国国家科学基金会;
关键词
ADIPONECTIN; AMPK; EMODIN; PPAR; MULTIMERIZATION; SECRETORY PROTEIN ADIPONECTIN; ADIPOSE-SPECIFIC PROTEIN; TYPE-2; DIABETIC-PATIENTS; RESPIRATORY COMPLEX-I; ADIPOCYTE DIFFERENTIATION; GLUCOSE-UPTAKE; PLASMA-CONCENTRATIONS; METABOLIC SYNDROME; CANCER CELLS; KINASE;
D O I
10.1002/jcb.24232
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Adiponectin is an important insulin-sensitizing adipokine with multiple beneficial effects on obesity-associated medical complications. It is secreted from adipocytes into circulation as high, medium, and low molecular weight forms (HMW, MMW, and LMW). Each oligomeric form of adiponectin exerts non-overlapping biological functions, with the HMW oligomer possessing the most potent insulin-sensitizing activity. In this study, we reported that emodin, a natural product and active ingredient of various Chinese herbs, activates AMPK in both 3T3-L1 adipocytes and 293T cells. Activation of AMPK by emodin promotes the assembly of HMW adiponectin and increases the ratio of HMW adiponectin to total adiponectin in 3T1-L1 adipocytes. Emodin might activate AMPK by an indirect mechanism similar to berberine. We also found that emodin activates PPAR? and promotes differentiation and adiponectin expression during differentiation of 3T3-L1 preadipocytes. Therefore, emodin is a novel AMPK activator with PPAR?-agonist activity. Our results demonstrate that the effects of emodin on adiponectin expression and multimerization are the ultimate effects resulting from both AMPK activation and PPAR? activation. The dual-activity makes emodin or the derivatives potential drug candidates for the treatment of type 2 diabetes and other obesity-related metabolic diseases. J. Cell. Biochem. 113: 35473558, 2012. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:3547 / 3558
页数:12
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