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Brain serotonin system in the coordination of food intake and body weight.

机译:脑5-羟色胺系统可以协调食物的摄入量和体重。

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摘要

An inverse relationship between brain serotonin and food intake and body weight has been known for more than 30 years. Specifically, augmentation of brain serotonin inhibits food intake, while depletion of brain serotonin promotes hyperphagia and weight gain. Through the decades, serotonin receptors have been identified and their function in the serotonergic regulation of food intake clarified. Recent refined genetic studies now indicate that a primary mechanism through which serotonin influences appetite and body weight is via serotonin 2C receptor (5-HT(2C)R) and serotonin 1B receptor (5-HT(1B)R) influencing the activity of endogenous melanocortin receptor agonists and antagonists at the melanocortin 4 receptor (MC4R). However, other mechanisms are also possible and the challenge of future research is to delineate them in the complete elucidation of the complex neurocircuitry underlying the serotonergic control of appetite and body weight.
机译:30多年来,人们已经知道大脑5-羟色胺与食物摄入量和体重之间存在反比关系。具体而言,增加大脑5-羟色胺会抑制食物摄入,而耗尽大脑5-羟色胺会促进食欲亢进和体重增加。在过去的几十年中,已经确定了5-羟色胺受体,并阐明了其在食物摄取的血清素能调节中的功能。现在,最近的改良遗传研究表明,血清素影响食欲和体重的主要机制是通过血清素2C受体(5-HT(2C)R)和血清素1B受体(5-HT(1B)R)影响内源性活性黑皮质素受体激动剂和拮抗剂在黑皮质素4受体(MC4R)。然而,其他机制也是可能的,未来研究的挑战是在完全阐明食欲和体重的血清素能控制基础的复杂神经回路中描绘它们。

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