No effect of Trp64Arg β3-adrenoceptor polymorphism on the plasma leptin concentration in Pima Indians

被引:4
|
作者
Snitker, S
Nicolson, M
Shuldiner, AR
Silver, K
Ravussin, E
机构
[1] NIDDK, Clin Diabet & Nutr Sect, NIH, Phoenix, AZ 85016 USA
[2] Univ Maryland, Baltimore, MD 21201 USA
[3] Amgen, Thousand Oaks, CA USA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 1998年 / 47卷 / 12期
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0026-0495(98)90081-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In rodents, administration of leptin promotes beta(3)-adrenergic stimulation of thermogenesis in brown adipose tissue. Conversely, administration of a beta(3)-adrenoceptor (beta(3)-AR) agonist decreases leptin mRNA expression and secretion, suggesting that leptin and sympathetic nervous system activity mediated through the beta(3)-AR comprise a negative-feedback loop. It has recently been proposed that a defect in the beta(3)-AR in humans may contribute to a resistance to the sympathetically mediated effects of leptin on thermogenesis and lipolysis, thus leading to obesity and type 2 diabetes mellitus. We thus hypothesized that the Trp64Arg variant in the human beta(3)-AR would be associated with elevated plasma leptin concentrations. We studied 101 healthy nondiabetic Pima Indians: 11 Arg64 homozygotes, 35 Trp64 homozygotes. and 55 heterozygotes. The fasting plasma leptin concentration as an absolute value or after adjustment for percent body fat and sex was not associated with the beta(3)-AR genotype. Thus, the data do not support an influence of the Trp64Arg variant on the plasma leptin concentration. Copyright (C) 1998 by W.B. Saunders Company.
引用
收藏
页码:1525 / 1527
页数:3
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