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灵香草对人 ether-a-go-go 相关基因 (HERG) K+ 通道的抑制作用。

Inhibition of the human ether-a-go-go-related gene (HERG) K+ channels by Lindera erythrocarpa.

机构信息

Department of Physiology, Institute of Bioscience and Biotechnology, Kangwon National University College of Medicine, Chuncheon, Korea.

出版信息

J Korean Med Sci. 2009 Dec;24(6):1089-98. doi: 10.3346/jkms.2009.24.6.1089. Epub 2009 Nov 9.

Abstract

Lindera erythrocarpa Makino (Lauraceae) is used as a traditional medicine for analgesic, antidote, and antibacterial purposes and shows anti-tumor activity. We studied the effects of Lindera erythrocarpa on the human ether-a-go-go-related gene (HERG) channel, which appears of importance in favoring cancer progression in vivo and determining cardiac action potential duration. Application of MeOH extract of Lindera erythrocarpa showed a dose-dependent decrease in the amplitudes of the outward currents measured at the end of the pulse (I(HERG)) and the tail currents of HERG (I(tail)). When the BuOH fraction and H(2)O fraction of Lindera erythrocarpa were added to the perfusate, both I(HERG) and I(tail) were suppressed, while the hexane fraction, CHCl(3) fraction, and EtOAc fraction did not inhibit either I(HERG) or I(tail). The potential required for half-maximal activation caused by EtOAc fraction, BuOH fraction, and H(2)O fraction shifted significantly. The BuOH fraction and H(2)O fraction (100 microg/mL) decreased g(max) by 59.6% and 52.9%, respectively. The H(2)O fraction- and BuOH fraction-induced blockades of I(tail) progressively decreased with increasing depolarization, showing the voltage-dependent block. Our findings suggest that Lindera erythrocarpa, a traditional medicine, blocks HERG channel, which could contribute to its anticancer and cardiac arrhythmogenic effect.

摘要

乌药(樟科)被用作传统药物,具有止痛、解毒和抗菌作用,并具有抗肿瘤活性。我们研究了乌药对人 ether-a-go-go 相关基因(HERG)通道的影响,该通道在促进体内肿瘤进展和确定心脏动作电位持续时间方面显得尤为重要。乌药甲醇提取物的应用表现出剂量依赖性地减小在脉冲结束时测量的外向电流(I(HERG))和 HERG 的尾电流(I(tail))的幅度。当乌药的正丁醇部分和水部分被添加到灌流液中时,I(HERG)和 I(tail)都被抑制,而己烷部分、CHCl(3)部分和 EtOAc 部分既不抑制 I(HERG)也不抑制 I(tail)。由 EtOAc 部分、正丁醇部分和水部分引起的半数最大激活所需的电位显著移位。正丁醇部分和水部分(100 microg/mL)分别使 g(max)降低 59.6%和 52.9%。水部分和正丁醇部分诱导的 I(tail)阻断随着去极化的增加而逐渐减小,表现出电压依赖性阻断。我们的研究结果表明,传统药物乌药可阻断 HERG 通道,这可能有助于其抗癌和致心律失常作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b0/2775857/932db835663b/jkms-24-1089-g001.jpg

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