Harrold Joanne A
Neuroendocrinology and Obesity Biology Unit, Department of Medicine, University of Liverpool, Liverpool, UK.
Curr Drug Targets. 2004 Apr;5(3):207-19. doi: 10.2174/1389450043490460.
Over the last decade, understanding of the circuits and molecules involved in the regulation of energy balance has expanded dramatically. A complex system has evolved which allows the brain to read, interpret and integrate a wide range of signals and to elicit appropriate changes in food intake and energy expenditure as a result of the information. A series of short-term signals derived from the gastrointestinal tract, such as cholecystokinin, govern meal size. Other hormones e.g. insulin and leptin, and circulating nutrients offer long-term regulation. These signals act at a variety of central nervous system sites, but the majority of pathways converge on the hypothalamus, which itself contains numerous peptides and neurotransmitters that influence feeding and energy expenditure. Mutations in key components of these circuits underlie some of the syndromes of genetic obesity in rodents, but are responsible for only a small percentage of human obesity--which is largely attributed to an adverse lifestyle. However, various abnormalities have been identified in dietary-obese rodents, which is the closest model to 'common' human obesity. The relevance of these to energy homeostasis in humans remains uncertain, but some are likely to emerge as therapeutic targets for the treatment of both obesity and eating disorders.
在过去十年中,人们对能量平衡调节所涉及的神经回路和分子的理解有了显著扩展。一个复杂的系统已经形成,它能使大脑读取、解读并整合各种信号,并根据这些信息引发食物摄入量和能量消耗的适当变化。一系列源自胃肠道的短期信号,如胆囊收缩素,控制着每餐的食量。其他激素,如胰岛素和瘦素,以及循环中的营养物质则提供长期调节。这些信号作用于中枢神经系统的多个部位,但大多数通路都汇聚于下丘脑,下丘脑本身就含有许多影响进食和能量消耗的肽类和神经递质。这些神经回路关键成分的突变是啮齿动物遗传性肥胖某些综合征的基础,但在人类肥胖中仅占很小比例——人类肥胖主要归因于不良生活方式。然而,在饮食诱导肥胖的啮齿动物中已发现各种异常情况,这是与“常见”人类肥胖最接近的模型。这些异常与人类能量稳态的相关性仍不确定,但其中一些可能会成为治疗肥胖症和饮食失调症的治疗靶点。