Suppr超能文献

瞬时受体电位香草酸亚型1拮抗剂的临床开发:针对疼痛通路中的关键点

Clinical development of TRPV1 antagonists: targeting a pivotal point in the pain pathway.

作者信息

Gunthorpe Martin J, Chizh Boris A

机构信息

Neurology Centre of Excellence for Drug Discovery, GlaxoSmithKline, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, UK.

出版信息

Drug Discov Today. 2009 Jan;14(1-2):56-67. doi: 10.1016/j.drudis.2008.11.005. Epub 2008 Dec 26.

Abstract

TRPV1 is a noxious heat, capsaicin (vanilloid) and acid receptor for which the development of antagonists represents a novel therapeutic approach for the treatment of pain. TRPV1 antagonists have entered early clinical development and initial reports indicate that they have demonstrated pharmacodynamic effects consistent with TRPV1 antagonist activity and anti-hyperalgesic action in humans. Should these effects extend to the relief of symptoms experienced by patients with chronic pain then this class of compounds may offer one of the first novel mechanisms of action for the treatment for pain for many years. In this article we will discuss recent progress and challenges in the field in this highly competitive area of drug discovery.

摘要

瞬时感受器电位香草酸亚型1(TRPV1)是一种有害热、辣椒素(香草酸类)和酸受体,针对该受体研发拮抗剂是一种治疗疼痛的新型治疗方法。TRPV1拮抗剂已进入早期临床开发阶段,初步报告表明,它们在人体中已展现出与TRPV1拮抗剂活性及抗痛觉过敏作用相符的药效学效应。如果这些效应能扩展至缓解慢性疼痛患者所经历的症状,那么这类化合物可能会成为多年来治疗疼痛的首批具有全新作用机制的药物之一。在本文中,我们将探讨在这个竞争激烈的药物研发领域中该领域的最新进展与挑战。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验