Electrical stimulation inactivates muscle acetyl-CoA carboxylase and increases AMP-activated protein kinase

被引:144
作者
Hutber, CA
Hardie, DG
Winder, WW
机构
[1] BRIGHAM YOUNG UNIV, DEPT ZOOL, PROVO, UT 84602 USA
[2] UNIV DUNDEE, DEPT BIOCHEM, DUNDEE DD1 4HN, SCOTLAND
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1997年 / 272卷 / 02期
基金
英国惠康基金;
关键词
skeletal muscle; fatty acid oxidation; muscle malonyl-CoA; phosphorylation of acetyl-CoA carboxylase;
D O I
10.1152/ajpendo.1997.272.2.E262
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Muscle malonyl-CoA decreases during exercise or electrical stimulation, the exercise-induced decline being accompanied by changes in the kinetic properties [maximal velocity (V-max), activation constant (K-a), and citrate concentration required to produce 50% V-max (K-0.5)] of acetyl-CoA carboxylase (ACC) and by an increase in the AMP-activated protein kinase activity (AMPK). This study was designed to ascertain whether the exercise-induced changes are contraction mediated and, if so, to follow the time course of these changes. The left sciatic nerve of rats was stimulated at 1 Hz for 0, 2, 5, 10, 20, or 30 min, and the gastrocnemius-plantaris muscle group was then excised, frozen in liquid nitrogen, and later analyzed for malonyl-CoA and other metabolites. ACC and AMPK activities were quantitated in ammonium sulfate precipitates from homogenates prepared from the frozen muscles. The V-max and K-a of ACC for citrate decreased and increased, respectively, over the first 10 min of stimulation, but significantly increased AMPK activity was not observed until 10 to 20 min of stimulation (P < 0.05). Stimulation increased estimated free AMP (P < 0.05). Thus exercise-induced changes in functional properties of ACC appear to be contraction mediated and are accompanied by increased AMPK activity and an increase in the estimated free AMP.
引用
收藏
页码:E262 / E266
页数:5
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