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瞬时受体电位通道作为缓解瘙痒的药物靶点。

TRP Channels as Drug Targets to Relieve Itch.

作者信息

Xie Zili, Hu Hongzhen

机构信息

Department of Anesthesiology, The Center for the Study of Itch, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Pharmaceuticals (Basel). 2018 Oct 6;11(4):100. doi: 10.3390/ph11040100.

Abstract

Although acute itch has a protective role by removing irritants to avoid further damage, chronic itch is debilitating, significantly impacting quality of life. Over the past two decades, a considerable amount of stimulating research has been carried out to delineate mechanisms of itch at the molecular, cellular, and circuit levels. There is growing evidence that transient receptor potential (TRP) channels play important roles in itch signaling. The purpose of this review is to summarize our current knowledge about the role of TRP channels in the generation of itch under both physiological and pathological conditions, thereby identifying them as potential drug targets for effective anti-itch therapies.

摘要

尽管急性瘙痒通过清除刺激物以避免进一步损伤而具有保护作用,但慢性瘙痒使人衰弱,会显著影响生活质量。在过去二十年中,人们开展了大量激动人心的研究,以在分子、细胞和回路水平阐明瘙痒的机制。越来越多的证据表明,瞬时受体电位(TRP)通道在瘙痒信号传导中发挥重要作用。本综述的目的是总结我们目前关于TRP通道在生理和病理条件下瘙痒产生中作用的认识,从而将它们确定为有效抗瘙痒治疗的潜在药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d2/6316386/368b348c9505/pharmaceuticals-11-00100-g001.jpg

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