Liu Zhao-qian, Mo Wei, Huang Qiong, Zhou Hong-hao
Institut eof Clinical Pharmacology, Xiangya School of Medicine, Central South University, Changsha 410078, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Jun;32(3):359-67.
The prevalent rates of overweight and obesity are steadily increasing all over the world. Previous studies of some candidate genes have indicated that most of the genes are associated with obesity in human adipose tissue. As much as 40% of the variations in body mass could be attributed to genetic difference. The beta-adrenergic receptor (beta-AR) plays a major role in the regulation of energy balance in humans. A high sympathetic nervous system activity has been shown to be associated with obesity and is believed to have pathogenetic relevance. Several common single nucleotide polymorphisms (SNPs) including Gly389Arg in beta(1)-AR, Gln27Glu in beta(2)-AR, and Trp64Arg in beta(3)-AR in humans could alter receptor function and these variations of beta-ARs were shown to have certain association with obesity. Here we summarize the genetic polymorphisms of human beta-ARs and their potential impacts to obesity.
全球超重和肥胖的流行率正在稳步上升。先前对一些候选基因的研究表明,大多数基因与人类脂肪组织中的肥胖有关。体重差异中多达40%可归因于基因差异。β-肾上腺素能受体(β-AR)在人类能量平衡调节中起主要作用。高交感神经系统活性已被证明与肥胖有关,并且被认为具有致病相关性。人类中几种常见的单核苷酸多态性(SNP),包括β1-AR中的Gly389Arg、β2-AR中的Gln27Glu和β3-AR中的Trp64Arg,可改变受体功能,并且这些β-AR的变异显示与肥胖有一定关联。在此,我们总结人类β-AR的基因多态性及其对肥胖的潜在影响。