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迈向对药物心脏毒性机制更广泛的认识。

Toward a broader view of mechanisms of drug cardiotoxicity.

作者信息

Mamoshina Polina, Rodriguez Blanca, Bueno-Orovio Alfonso

机构信息

Deep Longevity Limited, Hong Kong.

Department of Computer Science, BHF Centre of Research Excellence, University of Oxford, Oxford, UK.

出版信息

Cell Rep Med. 2021 Mar 16;2(3):100216. doi: 10.1016/j.xcrm.2021.100216.

Abstract

Cardiotoxicity, defined as toxicity that affects the heart, is one of the most common adverse drug effects. Numerous drugs have been shown to have the potential to induce lethal arrhythmias by affecting cardiac electrophysiology, which is the focus of current preclinical testing. However, a substantial number of drugs can also affect cardiac function beyond electrophysiology. Within this broader sense of cardiotoxicity, this review discusses the key drug-protein interactions known to be involved in cardiotoxic drug response. We cover adverse effects of anticancer, central nervous system, genitourinary system, gastrointestinal, antihistaminic, anti-inflammatory, and anti-infective agents, illustrating that many share mechanisms of cardiotoxicity, including contractility, mitochondrial function, and cellular signaling.

摘要

心脏毒性被定义为影响心脏的毒性,是最常见的药物不良反应之一。许多药物已被证明有可能通过影响心脏电生理来诱发致命性心律失常,这是当前临床前测试的重点。然而,相当数量的药物也可在电生理之外影响心脏功能。在这种更广泛的心脏毒性概念范围内,本综述讨论了已知参与心脏毒性药物反应的关键药物 - 蛋白质相互作用。我们涵盖了抗癌药、中枢神经系统药物、泌尿生殖系统药物、胃肠道药物、抗组胺药、抗炎药和抗感染药的不良反应,表明许多药物具有共同的心脏毒性机制,包括收缩性、线粒体功能和细胞信号传导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b9/7974548/61f51f474421/fx1.jpg

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