黑色素浓缩激素受体1的生物学检查:来自下丘脑的多任务。

Laura L Rokosz, Douglas W Hobbs
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摘要

自从发现了促氧神经肽黑色素浓缩激素(MCH)的第一个受体以来,MCH受体MCHR1一直被积极地用于治疗肥胖的治疗干预。与野生型小鼠相比,靶向缺失MCHR1或其同源配体MCH的小鼠通常体重和脂肪量下降,并且对饮食诱导的肥胖具有抵抗力。与对照动物相比,经脑室内灌注MCH或过表达MCH或MCHR1的小鼠表现出体重增加。MCHR1也是瘦素信号传导的中心靶点,似乎是胰岛素抵抗的中介。MCH和MCHR1在大鼠大脑中的分布,在控制食欲和饱腹感的区域之外,导致发现MCH信号参与其他功能,如情绪和压力。本文将详细介绍MCH和MCHR1如何控制多种生理功能的生物学研究。还将评估用于临床的MCHR1拮抗剂的开发现状。考虑到肥胖与其相关的许多疾病之间的实质性联系,一种可以用于治疗多种疾病的单一药物将受到欢迎。
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Biological examination of melanin concentrating hormone receptor 1: multi-tasking from the hypothalamus.

Since its discovery as the first receptor for the orexigenic neuropeptide melanin-concentrating hormone (MCH), the MCH receptor, MCHR1, has been actively pursued for therapeutic intervention in the treatment of obesity. Mice with targeted deletion of MCHR1 or its cognate ligand, MCH, generally have decreased body weight and fat mass and are resistant to diet-induced obesity compared with their wild-type counterparts. Mice treated via intracerebroventricular infusion with MCH, or that overexpress MCH or MCHR1, exhibit weight gain compared with control animals. MCHR1 is also a central target of leptin signaling and appears to be a mediator of insulin resistance. The distribution of MCH and MCHR1 in rat brain, outside of regions that control appetite and satiety, has led to the finding that MCH signaling participates in other functions such as emotion and stress. This review will describe in detail the biological studies that show how MCH and MCHR1 control numerous physiological functions. The current status of the development of MCHR1 antagonists for clinical use will also be assessed. Given the substantial link between obesity and its many associated afflictions, a single pharmaceutical agent that could be used to treat multiple pathologies would be welcome.

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