Pachymic acid stimulates glucose uptake through enhanced GLUT4 expression and translocation

过剩4 葡萄糖摄取 葡萄糖转运蛋白 化学 安普克 生物化学 胰岛素 3T3-L1 生物 脂肪细胞 磷酸化 脂肪组织 内分泌学 蛋白激酶A
作者
Yu-Chuan Huang,Wen-Liang Chang,Su-Fen Huang,Cheng-Yu Lin,Hang‐Ching Lin,Tsu‐Chung Chang
出处
期刊:European Journal of Pharmacology [Elsevier]
卷期号:648 (1-3): 39-49 被引量:82
标识
DOI:10.1016/j.ejphar.2010.08.021
摘要

In an effort to investigate the effect and mechanism of Poria cocos on glucose uptake, six lanostane-type triterpenoids were isolated and analyzed. Among them, pachymic acid displayed the most significant stimulating activity on glucose uptake in 3T3-L1 adipocytes. The effect of pachymic acid on the expression profile of glucose transporters in differentiated 3T3-L1 adipocytes was also analyzed. Our results demonstrated that pachymic acid induced an increase in GLUT4, but not GLUT1, expression at both the mRNA and protein levels. The role of GLUT4 was further confirmed using the lentiviral vector-derived GLUT4 short hairpin RNA (shRNA). The stimulating activity of pachymic acid on glucose uptake was abolished when the endogenous GLUT4 expression was suppressed in 3T3-L1 adipocytes. In addition to increased GLUT4 expression, pachymic acid stimulated GLUT4 redistribution from intracellular vesicles to the plasma membrane in adipocytes. Exposure of the differentiated adipocytes to pachymic acid increased the phosphorylation of insulin receptor substrate (IRS)-1, AKT and AMP-activated kinase (AMPK). The involvement of PI3K and AMPK in the action of pachymic acid was further confirmed as PI3K and AMPK inhibitors completely blocked the pachymic acid-mediated activities in adipocytes. In addition, pachymic acid was shown to induce triglyceride accumulation and inhibit lipolysis in differentiated adipocytes. Taken together, we demonstrated the insulin-like activities of this compound in stimulating glucose uptake, GLUT4 gene expression and translocation, and promoting triglyceride accumulation in adipocytes. Our study provides important insights into the underlying mechanism of hypoglycemic activity of P. cocos.
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