Saponara Simona, Fusi Fabio, Iovinelli Daniele, Ahmed Amer, Trezza Alfonso, Spiga Ottavia, Sgaragli Giampietro, Valoti Massimo
Dipartimento di Scienze della Vita, Università degli Studi di Siena, via A. Moro 2, 53100, Siena, Italy.
Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, via A. Moro 2, 53100, Siena, Italy.
Eur J Pharmacol. 2021 May 15;899:174030. doi: 10.1016/j.ejphar.2021.174030. Epub 2021 Mar 13.
The cardiac action potential is regulated by several ion channels. Drugs capable to block these channels, in particular the human ether-à-go-go-related gene (hERG) channel, also known as K11.1 channel, may lead to a potentially lethal ventricular tachyarrhythmia called "Torsades de Pointes". Thus, evaluation of the hERG channel off-target activity of novel chemical entities is nowadays required to safeguard patients as well as to avoid attrition in drug development. Flavonoids, a large class of natural compounds abundantly present in food, beverages, herbal medicines, and dietary food supplements, generally escape this assessment, though consumed in consistent amounts. Continuously growing evidence indicates that these compounds may interact with the hERG channel and block it. The present review, by examining numerous studies, summarizes the state-of-the-art in this field, describing the most significant examples of direct and indirect inhibition of the hERG channel current operated by flavonoids. A description of the molecular interactions between a few of these natural molecules and the Rattus norvegicus channel protein, achieved by an in silico approach, is also presented.
心脏动作电位受多种离子通道调节。能够阻断这些通道的药物,特别是人类醚 - 去极化相关基因(hERG)通道(也称为K11.1通道),可能会导致一种潜在致命的室性快速心律失常,称为“尖端扭转型室速”。因此,如今为了保护患者以及避免药物开发过程中的淘汰,需要评估新型化学实体的hERG通道脱靶活性。黄酮类化合物是一类大量存在于食物、饮料、草药和膳食补充剂中的天然化合物,尽管人们会持续大量摄入,但通常会逃过这种评估。越来越多的证据表明,这些化合物可能与hERG通道相互作用并阻断它。本综述通过考察大量研究,总结了该领域的最新进展,描述了黄酮类化合物对hERG通道电流直接和间接抑制的最重要实例。还介绍了通过计算机模拟方法得出的其中一些天然分子与褐家鼠通道蛋白之间分子相互作用的描述。