TRPC通道的药理作用及其在心血管和代谢医学中的潜力。

IF 11.2 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Robin S Bon, David J Wright, David J Beech, Piruthivi Sukumar
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引用次数: 10

摘要

瞬时受体电位规范(TRPC)蛋白组装形成同源或异四聚体,可渗透到K+, Na+和Ca2+的非选择性阳离子通道。TRPC通道被认为是物理和化学环境刺激的复杂集成商。尽管对TRPC通道的基本生理作用的了解尚不完整,但它们在神经系统、肾脏和心血管系统的各种病理机制和状况中的意义,加上TRPC敲除或TRPC通道抑制缺乏主要不良反应,正在推动TRPC通道调节剂作为潜在治疗药物的研究。在这里,我们回顾了最有前途的小分子TRPC通道调节剂,对它们的作用方式的理解,以及它们在心血管和代谢疾病的研究和治疗中的潜力。
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 TRPC Channels and Its Potential in Cardiovascular and Metabolic Medicine.

Transient receptor potential canonical (TRPC) proteins assemble to form homo- or heterotetrameric, nonselective cation channels permeable to K+, Na+, and Ca2+. TRPC channels are thought to act as complex integrators of physical and chemical environmental stimuli. Although the understanding of essential physiological roles of TRPC channels is incomplete, their implication in various pathological mechanisms and conditions of the nervous system, kidneys, and cardiovascular system in combination with the lack of major adverse effects of TRPC knockout or TRPC channel inhibition is driving the search of TRPC channel modulators as potential therapeutics. Here, we review the most promising small-molecule TRPC channel modulators, the understanding of their mode of action, and their potential in the study and treatment of cardiovascular and metabolic disease.

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来源期刊
CiteScore
27.80
自引率
0.00%
发文量
53
期刊介绍: Since 1961, the Annual Review of Pharmacology and Toxicology has been a comprehensive resource covering significant developments in pharmacology and toxicology. The journal encompasses various aspects, including receptors, transporters, enzymes, chemical agents, drug development science, and systems like the immune, nervous, gastrointestinal, cardiovascular, endocrine, and pulmonary systems. Special topics are also featured in this annual review.
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