A role for AMPK in the inhibition of glucose-6-phosphate dehydrogenase by polyunsaturated fatty acids

被引:36
作者
Kohan, Alison B. [1 ]
Talukdar, Indrani [1 ]
Walsh, Callee M. [1 ]
Salati, Lisa M. [1 ]
机构
[1] W Virginia Univ, Dept Biochem, Morgantown, WV 26506 USA
基金
美国国家卫生研究院;
关键词
Polyunsaturated fatty acids; Lipogenesis; Primary hepatocytes; AMP-activated protein kinase; ACTIVATED PROTEIN-KINASE; ACETYL-COA CARBOXYLASE; GLUCOSE; CELLS; LIVER; EXPRESSION; INDUCTION; MECHANISM; HORMONES; ENZYMES;
D O I
10.1016/j.bbrc.2009.07.130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both polyunsaturated fatty acids and AMPK promote energy partitioning away from energy consuming processes, such as fatty acid synthesis, towards energy generating processes, such as beta-oxidation. In this report, we demonstrate that arachidonic acid activates AMPK in primary rat hepatocytes, and that this effect is p38 MAPK-dependent. Activation of AMPK mimics the inhibition by arachidonic acid of the insulin-mediated induction of G6PD. Similar to intracellular signaling by arachidonic acid, AMPK decreases insulin signal transduction, increasing Ser(307) phosphorylation of IRS-1 and a subsequent decrease in AKT phosphorylation. Overexpression of dominant-negative AMPK abolishes the effect of arachidonic acid on G6PD expression. These data suggest a role for AMPK in the inhibition of G6PD by polyunsaturated fatty acids. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:117 / 121
页数:5
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