胰岛素
胰岛素受体
磷酸烯醇丙酮酸羧激酶
糖异生
胰岛素受体底物
葡萄糖转运蛋白
化学
磷酸化
内科学
生物化学
酪氨酸磷酸化
信号
内分泌学
信号转导
葡萄糖摄取
受体酪氨酸激酶
酪氨酸
生物
IRS2
碳水化合物代谢
GRB10型
细胞生物学
酪氨酸激酶
运输机
受体
过剩4
激酶
糖原分解
细胞信号
下调和上调
蛋白激酶C
蛋白激酶A
作者
Isabel Cordero‐Herrera,María Ángeles Martín,Laura Bravo,Luis Goya,Sonia Ramos
标识
DOI:10.1002/mnfr.201200500
摘要
Scope Cocoa and (–)‐epicatechin ( EC ), a main cocoa flavanol, have been suggested to exert beneficial effects in diabetes, but the mechanism for their insulin‐like effects remains unknown. In this study, the modulation of insulin signalling by EC and a cocoa phenolic extract ( CPE ) on hepatic H ep G 2 cells was investigated by analysing key proteins of the insulin pathways, namely insulin receptor, insulin receptor substrate ( IRS ) 1 and 2, PI 3 K / AKT and 5′‐ AMP ‐activated protein kinase ( AMPK ), as well as the levels of the glucose transporter GLUT ‐2 and the hepatic glucose production. Methods and results EC and CPE enhanced the tyrosine phosphorylation and total insulin receptor, IRS ‐1 and IRS ‐2 levels and activated the PI 3 K / AKT pathway and AMPK in H ep G 2 cells. CPE also enhanced the levels of GLUT ‐2. Interestingly, EC and CPE modulated the expression of phosphoenolpyruvate carboxykinase, a key protein involved in the gluconeogenesis, leading to a diminished glucose production. In addition, EC ‐ and CPE ‐regulated hepatic gluconeogenesis was prevented by the blockage of AKT and AMPK . Conclusion Our data suggest that EC and CPE strengthen the insulin signalling by activating key proteins of that pathway and regulating glucose production through AKT and AMPK modulation in H ep G 2 cells.
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