Glucose and insulin-induced inhibition of fatty acid oxidation: The glucose fatty acid cycle reversed

被引:146
作者
Sidossis, LS
Wolfe, RR
机构
[1] UNIV TEXAS, MED BRANCH, DEPT SURG, GALVESTON, TX 77550 USA
[2] UNIV TEXAS, MED BRANCH, DEPT ANESTHESIOL, GALVESTON, TX 77550 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1996年 / 270卷 / 04期
关键词
obesity; diabetes; mitochondria; malonyl-coenzyme A; carnitine acetyltransferase;
D O I
10.1152/ajpendo.1996.270.4.E733
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study we have investigated a hypothesis that proposes the reverse of the so-called ''glucose-fatty acid cycle,'' i.e., that accelerated carbohydrate metabolism directly inhibits fatty acid oxidation. We studied normal volunteers in the basal state and during a hyperinsulinemic, hyperglycemic clamp (plasma insulin = 1,789 +/- 119 pmol/l, plasma glucose = 7.7 +/- 0.2 mmol/l). We quantified fat oxidation using indirect calorimetry and stable isotopes ([1-C-13]oleate). Plasma oleate enrichment and free fatty acid (FFA) concentration were kept constant by means of infusion of lipids and heparin. Glucose oxidation increased from basal 6.2 +/- 0.8 to 22.3 +/- 1.4 mu mol . kg(-1). min(-1) during the clamp (P < 0.01). Total (indirect calorimetry) and plasma fatty acid oxidation (isotopic determination) decreased from 2.6 +/- 0.2 to 0.4 +/- 0.3 (P < 0.01) and 2.2 +/- 0.2 to 1.4 +/- 0.1 mu mol . kg(-1). min(-1) (P < 0.05), respectively. We conclude that under the conditions of the present experiment, glucose and/or insulin directly inhibits fatty acid oxidation. Our findings suggest that, contrary to the prediction of the glucose-fatty acid cycle, the intracellular availability of glucose (rather than FFA) determines the nature of substrate oxidation in human subjects.
引用
收藏
页码:E733 / E738
页数:6
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