Lack of skeletal muscle uncoupling protein 2 and 3 mRNA induction during fasting in type-2 diabetic subjects

被引:29
作者
Vidal, H
Langin, D
Andreelli, F
Millet, L
Larrouy, D
Laville, M
机构
[1] Fac Med Rene Laennec, INSERM U449, F-69372 Lyon, France
[2] Fac Med Rene Laennec, Ctr Rech Nutr Humaine Lyon, F-69372 Lyon, France
[3] Univ Toulouse 3, Inst Louis Bugnard, INSERM U317, F-31403 Toulouse, France
[4] Hop Edouard Herriot, Serv Endocrinol Diabetol & Nutr, F-69437 Lyon, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1999年 / 277卷 / 05期
关键词
obesity; calorie restriction; nonesterified fatty acid; lipolysis;
D O I
10.1152/ajpendo.1999.277.5.E830
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Skeletal muscle uncoupling protein 2 and 3 (UCP-2 and UCP-3) mRNA levels are increased during calorie restriction in lean and nondiabetic obese subjects. In this work, we have investigated the effect of a 5-day hypocaloric diet (1,045 kJ/day) on UCP-2 and UCP-3 gene expression in the skeletal muscle of type-2 diabetic obese patients. Before the diet, UCP-2 and UCP-3 mRNA levels were more abundant in diabetic than in nondiabetic subjects. The long (UCP-3(L)) and short (UCP-3(S)) forms of UCP-3 transcripts were expressed at similar levels in nondiabetic subjects, but UCP-3(S) transcripts were twofold more abundant than UCP-3L transcripts in the muscle of diabetic patients. Calorie restriction induced a two- to threefold increase in UCP-2 and UCP-3 mRNA levels in nondiabetic patients. No change was observed in type-2 diabetic patients. Variations in plasma nonesterified fatty acid level were positively correlated with changes in skeletal muscle UCP-3(L) (r = 0.6, P < 0.05) and adipose tissue hormone-sensitive lipase (r = 0.9, P < 0.001) mRNA levels. Lack of increase in plasma nonesterified fatty acid level and in hormone-sensitive lipase upregulation in diabetic patients during the diet strengthens the hypothesis that fatty acids are associated with the upregulation of uncoupling proteins during calorie restriction.
引用
收藏
页码:E830 / E837
页数:8
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