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影响调节能量平衡和肥胖的系统的发育基因与环境相互作用。

Developmental gene x environment interactions affecting systems regulating energy homeostasis and obesity.

机构信息

Neurology Service, VA Medical Center, E. Orange, NJ 07018-1095, USA.

出版信息

Front Neuroendocrinol. 2010 Jul;31(3):270-83. doi: 10.1016/j.yfrne.2010.02.005. Epub 2010 Mar 3.

Abstract

Most human obesity is inherited as a polygenic trait which is largely refractory to medical therapy because obese individuals avidly defend their elevated body weight set-point. This set-point is mediated by an integrated neural network that controls energy homeostasis. Epidemiological studies suggest that perinatal and pre-pubertal environmental factors can promote offspring obesity. Rodent studies demonstrate the important interactions between genetic predisposition and environmental factors in promoting obesity. This review covers issues of development and function of neural systems involved in the regulation of energy homeostasis and the roles of leptin and insulin in these processes, the ways in which interventions at various phases from gestation, lactation and pre-pubertal stages of development can favorably and unfavorably alter the development of obesity n offspring. These studies suggest that early identification of obesity-prone humans and of the factors that can prevent them from becoming obese could provide an effective strategy for preventing the world-wide epidemic of obesity.

摘要

大多数人类肥胖是作为一种多基因特征遗传的,由于肥胖个体强烈地捍卫他们升高的体重基准点,这种特征在很大程度上对医学治疗有抗性。这个基准点是由一个控制能量平衡的综合神经网络介导的。流行病学研究表明,围产期和青春期前的环境因素可以促进后代肥胖。啮齿动物研究表明,遗传易感性和环境因素之间的重要相互作用促进肥胖。这篇综述涵盖了参与调节能量平衡的神经网络的发育和功能的问题,以及瘦素和胰岛素在这些过程中的作用,在妊娠、哺乳期和青春期前发育的各个阶段进行干预可以有利和不利地改变肥胖后代的发展的方式。这些研究表明,早期识别肥胖易感人群以及可以防止他们肥胖的因素,可以为预防肥胖的全球流行提供有效的策略。

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