首页> 外文OA文献 >Cocoa flavonoids improve insulin signalling and modulate glucose production via AKT and AMPK in HepG2 cells
【2h】

Cocoa flavonoids improve insulin signalling and modulate glucose production via AKT and AMPK in HepG2 cells

机译:可可黄酮通过HepG2细胞中的AKT和AMPK改善胰岛素信号传导并调节葡萄糖生成

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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 HepG2 cells was investigated by analysing key proteins of the insulin pathways, namely insulin receptor, insulin receptor substrate (IRS) 1 and 2, PI3K/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 PI3K/AKT pathway and AMPK in HepG2 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 HepG2 cells. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
机译:范围:已建议可可和主要的可可黄烷醇(-)-表儿茶素(EC)在糖尿病中发挥有益作用,但其类胰岛素作用的机制尚不清楚。在这项研究中,通过分析胰岛素途径的关键蛋白,即胰岛素受体,胰岛素受体底物(IRS)1和2,PI3K / AKT和5'-AMP激活的蛋白激酶(AMPK)以及葡萄糖转运蛋白GLUT-2的水平和肝葡萄糖的产生。方法和结果:EC和CPE增强了HepG2细胞中的酪氨酸磷酸化和总胰岛素受体,IRS-1和IRS-2水平,并激活了PI3K / AKT途径和AMPK。 CPE还提高了GLUT-2的水平。有趣的是,EC和CPE调节了磷酸烯醇丙酮酸羧化激酶(一种参与糖异生的关键蛋白)的表达,导致葡萄糖生成减少。此外,AKT和AMPK的阻滞阻止了EC和CPE调节的肝糖异生。结论:我们的数据表明EC和CPE通过激活该途径的关键蛋白并通过AKT和AMPK调节HepG2细胞中的葡萄糖产生来增强胰岛素信号传导。 ©2013 WILEY-VCH Verlag GmbH&Co. KGaA,Weinheim。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号