Analysis of energy expenditure at different ambient temperatures in mice lacking DGAT1

被引:63
|
作者
Chen, HC
Ladha, Z
Smith, SJ
Farese, RV
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[3] Gladstone Inst Cardiovasc Dis, San Francisco, CA 94103 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2003年 / 284卷 / 01期
关键词
fasting; glycogen; hypoglycemia; thermoregulation; triglyceride synthesis; uncoupling protein 1; acyl-CoA : diacylglycerol; acyltransferase; 1;
D O I
10.1152/ajpendo.00248.2002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mice lacking acyl-CoA: diacylglycerol acyltransferase 1 (DGAT1), a key enzyme in triglyceride synthesis, have increased energy expenditure and therefore are resistant to obesity. Because ambient temperature can significantly affect energy expenditure in mice, we undertook these studies to determine the effects of different ambient temperatures on energy expenditure, food intake, and thermoregulation in DGAT1-deficient [Dgat1(-/-)] mice. Dgat1(-/-) mice had increased energy expenditure irrespective of changes in the ambient temperature. Although core temperature was normal, surface temperature was increased in Dgat1(-/-) mice, most likely reflecting an active mechanism to dissipate heat from increased thermogenesis. Dgat1(-/-) mice had increased food intake at baseline, and this hyperphagia became more pronounced upon exposure to cold. When fasted in a cold environment, Dgat1(-/-) mice developed hypothermia, which was associated with hypoglycemia. These results suggest that the hyperphagia in Dgat1(-/-) mice is a secondary mechanism that compensates for the increased utilization of fuel substrates. Our findings offer insights into the mechanisms of hyperphagia and increased energy expenditure in a murine model of obesity resistance.
引用
收藏
页码:E213 / E218
页数:6
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