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瘦素-黑皮质素信号通路在食物摄入控制中的作用。

The role of the leptin-melanocortin signalling pathway in the control of food intake.

作者信息

Beckers Sigri, Zegers Doreen, Van Gaal Luc F, Van Hul Wim

机构信息

Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.

出版信息

Crit Rev Eukaryot Gene Expr. 2009;19(4):267-87. doi: 10.1615/critreveukargeneexpr.v19.i4.20.

Abstract

Obesity is one of the most important health problems today. Obesity is mostly caused by a complex interaction between environmental and genetic factors. However, several monogenic forms of obesity also exist. The mutations causing these forms of obesity were all found in genes involved in the leptin-melanocortin pathway: leptin, leptin receptor, proopiomelanocortin, prohormone convertase 1, and melanocortin-4 receptor. Recently, several novel players with a role in this pathway have been identified and have increased our knowledge on the regulation of food intake. These include the melanocortin-3 receptor, BDNF, SIM1, and nesfatin-1. In this review, we will discuss the most important players involved in this pathway. We will focus on genetic studies concerning mouse models involving these genes and reported human variation in these genes. We intend to provide an extensive overview of all currently known proteins with a significant role in this pathway. Together, these data demonstrate the importance of this pathway in the regulation of food intake and the pathogenesis of obesity.

摘要

肥胖是当今最重要的健康问题之一。肥胖主要由环境因素和遗传因素之间的复杂相互作用引起。然而,也存在几种单基因形式的肥胖。导致这些肥胖形式的突变均在参与瘦素-促黑素细胞皮质素途径的基因中发现:瘦素、瘦素受体、阿黑皮素原、激素原转化酶1和促黑素细胞皮质素-4受体。最近,已鉴定出该途径中起作用的几个新因子,这增加了我们对食物摄入调节的认识。这些因子包括促黑素细胞皮质素-3受体、脑源性神经营养因子、SIM1和nesfatin-1。在本综述中,我们将讨论该途径中最重要的因子。我们将重点关注涉及这些基因的小鼠模型的遗传学研究以及报道的这些基因中的人类变异。我们打算全面概述目前已知的在该途径中起重要作用的所有蛋白质。总之,这些数据证明了该途径在食物摄入调节和肥胖发病机制中的重要性。

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