血管紧张素通道的药理学

IF 4 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Michael Koval , Wyatt J. Schug , Brant E. Isakson
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引用次数: 10

摘要

Pannexin通道在调节炎症中发挥着基本作用,并与许多疾病有关,包括高血压、中风和神经性疼痛。因此,在药理学上阻断这些通道的能力是几种治疗方法的重要组成部分。对模型系统的药理学询问也为发现血管内皮素在细胞生理学中的新作用提供了一种手段。在这里,我们回顾了可用于阻断pannexin通道的药物的现状,重点是作用于pannexin1的化学药物和肽模拟物。讨论了在实验系统中解释pannexin药理学结果的指导,以及不同药物的优势和注意事项,包括临床应用的特异性和可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacology of pannexin channels

Pannexin channels play fundamental roles in regulating inflammation and have been implicated in many diseases including hypertension, stroke, and neuropathic pain. Thus, the ability to pharmacologically block these channels is a vital component of several therapeutic approaches. Pharmacologic interrogation of model systems also provides a means to discover new roles for pannexins in cell physiology. Here, we review the state of the art for agents that can be used to block pannexin channels, with a focus on chemical pharmaceuticals and peptide mimetics that act on pannexin 1. Guidance on interpreting results obtained with pannexin pharmacologics in experimental systems is discussed, as well as strengths and caveats of different agents, including specificity and feasibility of clinical application.

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来源期刊
CiteScore
8.80
自引率
2.50%
发文量
131
审稿时长
4-8 weeks
期刊介绍: Current Opinion in Pharmacology (COPHAR) publishes authoritative, comprehensive, and systematic reviews. COPHAR helps specialists keep up to date with a clear and readable synthesis on current advances in pharmacology and drug discovery. Expert authors annotate the most interesting papers from the expanding volume of information published today, saving valuable time and giving the reader insight on areas of importance.
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