AICA riboside increases AMP-activated protein kinase, fatty acid oxidation, and glucose uptake in rat muscle

被引:811
作者
Merrill, GF
Kurth, EJ
Hardie, DG
Winder, WW
机构
[1] Brigham Young Univ, Dept Zool, Provo, UT 84602 USA
[2] Rutgers State Univ, Dept Biol Sci, New Brunswick, NJ 08903 USA
[3] Univ Dundee, Dept Biochem, Dundee DD1 4HN, Scotland
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1997年 / 273卷 / 06期
关键词
acetyl-CoA carboxylase; malonyl-CoA; palmitate oxidation; 5-aminoimidazole-4-carboxamide riboside; ZMP;
D O I
10.1152/ajpendo.1997.273.6.E1107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
5-Aminoimidazole-4-carboxamide ribonucleoside (AICAR) has previously been reported to be taken up into cells and phosphorylated to form ZMP, an analog of 5'-AMP. This study was designed to determine whether AICAR can activate AMP-activated protein kinase (AMPK) in skeletal muscle with consequent phosphorylation of acetyl-CoA carboxylase (ACC), decrease in malonyl-CoA, and increase in fatty acid oxidation. Rat hindlimbs were perfused with Krebs-Henseleit bicarbonate containing 4% bovine serum albumin, washed bovine red blood cells, 200 mu U/ml insulin, and 10 mM glucose with or without AICAR (0.5-2.0 mM). Perfusion with medium containing AICAR was found to activate AMPK in skeletal muscle, inactivate ACC, and decrease malonyl-CoA. Hindlimbs perfused with 2 mM AICAR for 45 min exhibited a 2.8-fold increase in fatty acid oxidation and a significant increase in glucose uptake. No difference was observed in oxygen uptake in AICAR vs. control hindlimb. These results provide evidence that decreases in muscle content of malonyl-CoA can increase the rate of fatty acid oxidation.
引用
收藏
页码:E1107 / E1112
页数:6
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