Targeting TRPV3 for the Development of Novel Analgesics.

Q3 Medicine
Susan M Huang, Man-Kyo Chung
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引用次数: 22

Abstract

Decades of characterization of the transient receptor potential vanilloid subtype 1 (TRPV1) has led to the realization of its central role in thermosensation and pain perception. A large number of pharmaceutical companies have had interest in developing TPRV1 antagonists for the treatment of pain. The subsequent discovery of multiple other members of this TRPV family has not gone unnoticed. TRPV3 exhibits approximately 40% homology to TRPV1, and has common as well as distinct features from TRPV1 in channel physiology, expression and function. Here we review the current understanding of TRPV3 channel biology, activation, sensitization and the consequences of TRPV3 manipulation for thermosensation and nociception, as well as additional considerations regarding the expression of TRPV3 in the skin. We weigh in on the available evidence in the context of potential development of TRPV3 modulating agents as analgesics.

靶向TRPV3开发新型镇痛药。
几十年来对瞬时受体电位香草样蛋白亚型1 (TRPV1)的研究已经使人们认识到它在热感觉和疼痛感知中的核心作用。许多制药公司已经对开发用于治疗疼痛的TPRV1拮抗剂产生了兴趣。随后发现的该TRPV家族的多个其他成员并没有被忽视。TRPV3与TRPV1的同源性约为40%,在通道生理、表达和功能上与TRPV1既有共同的特征,也有不同的特征。在这里,我们回顾了目前对TRPV3通道生物学、激活、致敏和TRPV3操作对热感觉和伤害感受的影响的理解,以及关于TRPV3在皮肤中表达的其他考虑。我们在现有证据的背景下权衡TRPV3调节剂作为镇痛药的潜在发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Open Pain Journal
Open Pain Journal Medicine-Anesthesiology and Pain Medicine
CiteScore
0.80
自引率
0.00%
发文量
9
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