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肽类 G 蛋白偶联受体的非肽配体。

Nonpeptide ligands for peptidergic G protein-coupled receptors.

机构信息

Institute of Parasitology, McGill University, 21111 Lakeshore Road, Ste-Anne-de-Bellevue, QC, Canada.

出版信息

Adv Exp Med Biol. 2010;692:10-26. doi: 10.1007/978-1-4419-6902-6_2.

Abstract

Neuropeptides play essential roles in many physiological systems in vertebrates and invertebrates. Peptides per se are difficult to use as therapeutic agents, as they are generally very unstable in biological fluid environments and cross biological membranes poorly. Recognition that nonpeptide ligands for peptide receptors have clinical utility came from the discovery that opiates (such as morphine) act by binding to G protein-coupled receptors (GPCRs) for which the endogenous ligands are a family of neuropeptides (enkephalins and endorphins). Basic research has revealed a very large number of distinct neuropeptides that influence virtually every aspect of mammalian physiology and considerable effort has been expended in the pursuit of new drugs that act through peptidergic signaling systems. Although useful drugs have been found to affect various aspects ofneuropeptide biology, most work has been devoted to the discovery of nonpeptide ligands that act as agonists or antagonists at peptidergic GPCRs. Similar opportunities are apparent for the discovery of nonpeptide ligands that act on invertebrate GPCRs. A consideration of the knowledge gained from the process as conducted for mammalian peptidergic systems can inform and illuminate promising strategies for the discovery of new drugs for the treatment and control of pests and parasites.

摘要

神经肽在脊椎动物和无脊椎动物的许多生理系统中发挥着重要作用。肽本身作为治疗剂很难使用,因为它们在生物流体环境中通常非常不稳定,并且很难穿过生物膜。对肽受体的非肽配体具有临床用途的认识来自于这样一个发现,即阿片类药物(如吗啡)通过与 G 蛋白偶联受体(GPCR)结合而发挥作用,而 GPCR 的内源性配体是一类神经肽(脑啡肽和内啡肽)。基础研究揭示了大量不同的神经肽,这些神经肽几乎影响哺乳动物生理学的各个方面,并且在追求通过肽能信号系统发挥作用的新药方面付出了巨大努力。尽管已经发现了一些有用的药物来影响神经肽生物学的各个方面,但大多数工作都致力于发现作为肽能 GPCR 的激动剂或拮抗剂的非肽配体。对于发现作用于无脊椎动物 GPCR 的非肽配体,也有类似的机会。考虑从哺乳动物肽能系统进行的过程中获得的知识,可以为发现用于治疗和控制害虫和寄生虫的新药提供有希望的策略。

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