Kratz Jadel M, Grienke Ulrike, Scheel Olaf, Mann Stefan A, Rollinger Judith M
Department of Pharmacognosy, Faculty of Life Sciences, University of Vienna, Althanstraße 14, 1090 Vienna, Austria.
Nat Prod Rep. 2017 Aug 2;34(8):957-980. doi: 10.1039/c7np00014f.
Covering: 1996-December 2016The human Ether-à-go-go Related Gene (hERG) channel is a voltage-gated potassium channel playing an essential role in the normal electrical activity in the heart. It is involved in the repolarization and termination of action potentials in excitable cardiac cells. Mutations in the hERG gene and hERG channel blockage by small molecules are associated with increased risk of fatal arrhythmias. Several drugs have been withdrawn from the market due to hERG channel-related cardiotoxicity. Moreover, as a result of its notorious ligand promiscuity, this ion channel has emerged as an important antitarget in early drug discovery and development. Surprisingly, the hERG channel blocking profile of natural compounds present in frequently consumed botanicals (i.e. dietary supplements, spices, and herbal medicinal products) is not routinely assessed. This comprehensive review will address these issues and provide a critical compilation of hERG channel data for isolated natural products and extracts over the past two decades (1996-2016). In addition, the review will provide (i) a solid basis for the molecular understanding of the physiological functions of the hERG channel, (ii) the translational potential of in vitro/in vivo results to cardiotoxicity in humans, (iii) approaches for the identification of hERG channel blockers from natural sources, (iv) future perspectives for cardiac safety guidelines and their applications within phytopharmaceuticals and dietary supplements, and (v) novel applications of hERG channel modulation (e.g. as a drug target).
1996年至2016年12月
人类醚-à-去相关基因(hERG)通道是一种电压门控钾通道,在心脏的正常电活动中起着至关重要的作用。它参与可兴奋心脏细胞动作电位的复极化和终止。hERG基因突变以及小分子对hERG通道的阻断与致命性心律失常风险增加有关。由于与hERG通道相关的心脏毒性,几种药物已从市场上撤回。此外,由于其臭名昭著的配体混杂性,该离子通道已成为早期药物发现和开发中的一个重要反靶点。令人惊讶的是,常见食用植物药(即膳食补充剂、香料和草药产品)中天然化合物的hERG通道阻断情况并未常规评估。本综述将探讨这些问题,并对过去二十年(1996 - 2016年)分离出的天然产物和提取物的hERG通道数据进行批判性汇编。此外,该综述将提供:(i)对hERG通道生理功能进行分子理解的坚实基础;(ii)体外/体内结果转化为人类心脏毒性的潜力;(iii)从天然来源鉴定hERG通道阻滞剂的方法;(iv)心脏安全指南及其在植物药和膳食补充剂中的应用的未来展望;以及(v)hERG通道调节的新应用(例如作为药物靶点)。