Wang Taiyi, Xie Weiwei, Yu Jiahui, Ellory Clive, Wilkins Robert, Zhu Yan, Ma Yu-Ling
Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Front Pharmacol. 2019 Feb 6;10:70. doi: 10.3389/fphar.2019.00070. eCollection 2019.
Xin Su Ning (XSN) is a China patented and certified herbal medicine used to treat premature ventricular contractions (PVCs) since 2005. A recent completed clinical trial of 861 patients showed that XSN had similar PVC inhibition rate to the class I antiarrhythmic drug mexiletine, at 65.85% for XSN and 63.10% for mexiletine. We have previously reported that XSN prolongs action potential duration (APD) and suppresses action potential amplitude (APA) of the cardiac ventricular myocytes. In this report we aim to reveal the effect of XSN on the ionic channels that govern APD and APA, which would help to explain the cellular electrophysiological mechanism of XSN. Our main findings are: (1) On ECG recorded in isolated rat, in the presence of XSN the amplitude of R wave was significantly decreased and the amplitude of T wave was increased significantly; (2) XSN blocked hNaV1.5 channel stably transfected cell line in a dose-dependent manner with an IC of 0.18 ± 0.02 g/L; and (3) XSN suppresses hERG channels in a dose-dependent manner with an IC of 0.34 ± 0.01 g/L. In conclusion, the clinical antiarrhythmic efficacy of XSN is based on its class I and Class III antiarrhythmic properties by suppression hNaV1.5 channel and hERG channels, which are directly responsible for XSN's effect on APA suppression and APD prolongation.
心速宁(XSN)是一种自2005年起在中国获得专利并认证的用于治疗室性早搏(PVCs)的草药。最近一项针对861名患者完成的临床试验表明,XSN的PVC抑制率与I类抗心律失常药物美西律相似,XSN为65.85%,美西律为63.10%。我们之前报道过XSN可延长心室肌细胞的动作电位时程(APD)并抑制动作电位幅度(APA)。在本报告中,我们旨在揭示XSN对调控APD和APA的离子通道的影响,这将有助于解释XSN的细胞电生理机制。我们的主要发现如下:(1)在离体大鼠记录的心电图上,在XSN存在的情况下,R波幅度显著降低,T波幅度显著增加;(2)XSN以剂量依赖性方式阻断稳定转染hNaV1.5通道的细胞系,半数抑制浓度(IC)为0.18±0.02 g/L;(3)XSN以剂量依赖性方式抑制hERG通道,IC为0.34±0.01 g/L。总之,XSN的临床抗心律失常疗效基于其通过抑制hNaV1.5通道和hERG通道而具有的I类和III类抗心律失常特性,这直接导致了XSN对APA抑制和APD延长的作用。