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可可黄烷醇可减轻高糖诱导的胰岛素信号转导阻断,并调节人 HepG2 细胞的葡萄糖摄取和产生。

Cocoa flavonoids attenuate high glucose-induced insulin signalling blockade and modulate glucose uptake and production in human HepG2 cells.

机构信息

Department of Metabolism and Nutrition, Institute of Food Science and Technology and Nutrition (ICTAN), Consejo Superior de Investigaciones Científicas (CSIC), José Antonio Novais 10, Ciudad Universitaria, 28040 Madrid, Spain.

Department of Metabolism and Nutrition, Institute of Food Science and Technology and Nutrition (ICTAN), Consejo Superior de Investigaciones Científicas (CSIC), José Antonio Novais 10, Ciudad Universitaria, 28040 Madrid, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), ISCIII, Spain.

出版信息

Food Chem Toxicol. 2014 Feb;64:10-9. doi: 10.1016/j.fct.2013.11.014. Epub 2013 Nov 19.

Abstract

Insulin resistance is the primary characteristic of type 2 diabetes. Cocoa and its main flavanol, (-)-epicatechin (EC), display some antidiabetic effects, but the mechanisms for their preventive activities related to glucose metabolism and insulin signalling in the liver remain largely unknown. In the present work, the preventive effect of EC and a cocoa polyphenolic extract (CPE) on insulin signalling and on both glucose production and uptake are studied in insulin-responsive human HepG2 cells treated with high glucose. Pre-treatment of cells with EC or CPE reverted decreased tyrosine-phosphorylated and total levels of IR, IRS-1 and -2 triggered by high glucose. EC and CPE pre-treatment also prevented the inactivation of the PI3K/AKT pathway and AMPK, as well as the diminution of GLUT-2 levels induced by high glucose. Furthermore, pre-treatment of cells with EC and CPE avoided the increase in PEPCK levels and the diminished glucose uptake provoked by high glucose, returning enhanced levels of glucose production and decreased glycogen content to control values. These findings suggest that EC and CPE improved insulin sensitivity of HepG2 treated with high glucose, preventing or delaying a potential hepatic dysfunction through the attenuation of the insulin signalling blockade and the modulation of glucose uptake and production.

摘要

胰岛素抵抗是 2 型糖尿病的主要特征。可可及其主要黄烷醇((-)-表儿茶素(EC))显示出一些抗糖尿病作用,但它们在葡萄糖代谢和肝脏胰岛素信号转导方面的预防活性的机制在很大程度上仍然未知。在本工作中,研究了 EC 和可可多酚提取物(CPE)对胰岛素反应性人 HepG2 细胞在高葡萄糖处理下的胰岛素信号转导以及葡萄糖产生和摄取的预防作用。用 EC 或 CPE 预处理可逆转高葡萄糖引起的 IR、IRS-1 和 -2 的酪氨酸磷酸化和总水平降低。EC 和 CPE 预处理还可以防止高葡萄糖诱导的 PI3K/AKT 途径和 AMPK 的失活,以及 GLUT-2 水平的降低。此外,用 EC 和 CPE 预处理可避免高葡萄糖引起的 PEPCK 水平升高和葡萄糖摄取减少,使葡萄糖生成增加和糖原含量降低恢复到对照值。这些发现表明,EC 和 CPE 改善了高葡萄糖处理的 HepG2 的胰岛素敏感性,通过减弱胰岛素信号转导阻断和调节葡萄糖摄取和产生来预防或延迟潜在的肝功能障碍。

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