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孤儿G蛋白偶联受体与肥胖

Orphan G protein-coupled receptors and obesity.

作者信息

Xu Yan-Ling, Jackson Valerie R, Civelli Olivier

机构信息

Department of Pharmacology, University of California Irvine, 101 Theory Dr., Suite 200, Irvine, CA 92612, USA.

出版信息

Eur J Pharmacol. 2004 Oct 1;500(1-3):243-53. doi: 10.1016/j.ejphar.2004.07.029.

Abstract

The use of orphan G protein-coupled receptors (GPCRs) as targets to identify new transmitters has led over the last decade to the discovery of 12 novel neuropeptide families. Each one of these new neuropeptides has opened its own field of research, has brought new insights in distinct pathophysiological conditions and has offered new potentials for therapeutic applications. Interestingly, several of these novel peptides have seen their roles converge on one physiological response: the regulation of food intake and energy expenditure. In this manuscript, we discuss four deorphanized GPCR systems, the ghrelin, orexins/hypocretins, melanin-concentrating hormone (MCH) and neuropeptide B/neuropeptide W (NPB/NPW) systems, and review our knowledge of their role in the regulation of energy balance and of their potential use in therapies directed at feeding disorders.

摘要

在过去十年中,将孤儿G蛋白偶联受体(GPCRs)用作靶点来鉴定新的递质,已促使人们发现了12个新的神经肽家族。这些新神经肽中的每一个都开启了其自身的研究领域,为不同的病理生理状况带来了新的见解,并为治疗应用提供了新的潜力。有趣的是,这些新肽中的几种已发现它们的作用集中于一种生理反应:食物摄入和能量消耗的调节。在本手稿中,我们讨论了四种已解除孤儿身份的GPCR系统,即胃饥饿素、食欲素/下丘脑泌素、促黑素细胞激素(MCH)和神经肽B/神经肽W(NPB/NPW)系统,并综述了我们对它们在能量平衡调节中的作用以及它们在针对进食障碍的治疗中的潜在用途的认识。

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