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抗癫痫药物拉莫三嗪和丙戊酸可降低心脏钠电流。

The Anti-Epileptic Drugs Lamotrigine and Valproic Acid Reduce the Cardiac Sodium Current.

作者信息

Jia Lixia, Verkerk Arie O, Tan Hanno L

机构信息

Department of Clinical and Experimental Cardiology, Heart Center, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.

Department of Medical Biology, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.

出版信息

Biomedicines. 2023 Feb 7;11(2):477. doi: 10.3390/biomedicines11020477.

DOI:10.3390/biomedicines11020477
PMID:36831014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9953282/
Abstract

Anti-epileptic drugs (AEDs) are associated with increased risk of sudden cardiac death. To establish whether gabapentin, lamotrigine, levetiracetam, pregabalin, and valproic acid reduce the Na1.5 current, we conducted whole-cell patch-clamp studies to study the effects of the five AEDs on currents of human cardiac Na1.5 channels stably expressed in HEK293 cells, and on action potential (AP) properties of freshly isolated rabbit ventricular cardiomyocytes. Lamotrigine and valproic acid exhibited inhibitory effects on the Na1.5 current in a concentration-dependent manner with an IC of 142 ± 36 and 2022 ± 25 µM for lamotrigine and valproic acid, respectively. In addition, these drugs caused a hyperpolarizing shift of steady-state inactivation and a delay in recovery from inactivation. The changes on the Na1.5 properties were reflected by a reduction in AP upstroke velocity (43.0 ± 6.8% (lamotrigine) and 23.7 ± 10.6% (valproic acid) at 1 Hz) and AP amplitude; in contrast, AP duration was not changed. Gabapentin, levetiracetam, and pregabalin had no effect on the Na1.5 current. Lamotrigine and valproic acid reduce the Na1.5 current density and affect its gating properties, resulting in a decrease of the AP upstroke velocity. Gabapentin, levetiracetam, and pregabalin have no effects on the Na1.5 current.

摘要

抗癫痫药物(AEDs)与心脏性猝死风险增加有关。为确定加巴喷丁、拉莫三嗪、左乙拉西坦、普瑞巴林和丙戊酸是否会降低Na1.5电流,我们进行了全细胞膜片钳研究,以研究这五种AEDs对稳定表达于HEK293细胞中的人心脏Na1.5通道电流以及对新鲜分离的兔心室心肌细胞动作电位(AP)特性的影响。拉莫三嗪和丙戊酸对Na1.5电流呈浓度依赖性抑制作用,拉莫三嗪和丙戊酸的半数抑制浓度(IC)分别为142±36 μM和2022±25 μM。此外,这些药物导致稳态失活的超极化移位以及失活恢复延迟。Na1.5特性的变化表现为动作电位上升速度降低(1 Hz时,拉莫三嗪为43.0±6.8%,丙戊酸为23.7±10.6%)和动作电位幅度降低;相比之下,动作电位时程未改变。加巴喷丁、左乙拉西坦和普瑞巴林对Na1.5电流无影响。拉莫三嗪和丙戊酸降低Na1.5电流密度并影响其门控特性,导致动作电位上升速度降低。加巴喷丁、左乙拉西坦和普瑞巴林对Na1.5电流无影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/7ae0563e28dd/biomedicines-11-00477-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/c39ec84b9990/biomedicines-11-00477-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/67a0d2d77454/biomedicines-11-00477-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/e2a9c396f9d1/biomedicines-11-00477-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/3b6ea7f580d7/biomedicines-11-00477-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/7ae0563e28dd/biomedicines-11-00477-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/c39ec84b9990/biomedicines-11-00477-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/67a0d2d77454/biomedicines-11-00477-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/e2a9c396f9d1/biomedicines-11-00477-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/3b6ea7f580d7/biomedicines-11-00477-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f206/9953282/7ae0563e28dd/biomedicines-11-00477-g005.jpg

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