Methadone Blockade of Cardiac Inward Rectifier K+ Current Augments Membrane Instability and Amplifies U Waves on Surface ECGs: A Translational Study

Michael G Klein, M. Krantz, N. Fatima, A. Watters, Dayan Colon-Sanchez, R. Geiger, R. Goldstein, S. Solhjoo, P. Mehler, T. Flagg, M. Haigney
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引用次数: 4

Abstract

Background Methadone is associated with a disproportionate risk of sudden death and ventricular tachyarrhythmia despite only modest inhibition of delayed rectifier K+ current (I Kr), the principal mechanism of drug‐associated arrhythmia. Congenital defects of inward rectifier K+ current (I K1) have been linked to increased U‐wave amplitude on ECG and fatal arrhythmia. We hypothesized that methadone may also be a potent inhibitor of I K1, contributing to delayed repolarization and manifesting on surface ECGs as augmented U‐wave integrals. Methods and Results Using a whole‐cell voltage clamp, methadone inhibited both recombinant and native I K1 with a half‐maximal inhibitory concentration IC50) of 1.5 μmol/L, similar to that observed for I Kr block (half‐maximal inhibitory concentration of 2.9 μmol/L). Methadone modestly increased the action potential duration at 90% repolarization and slowed terminal repolarization at low concentrations. At higher concentrations, action potential duration at 90% repolarization lengthening was abolished, but its effect on terminal repolarization rose steadily and correlated with increased fluctuations of diastolic membrane potential. In parallel, patient ECGs were analyzed before and after methadone initiation, with 68% of patients having a markedly increased U‐wave integral compared with premethadone (lead V3; mean +38%±15%, P=0.016), along with increased QT and TPeak to TEnd intervals, likely reflective of I Kr block. Conclusions Methadone is a potent I K1 inhibitor that causes augmentation of U waves on surface ECG. We propose that increased membrane instability resulting from I K1 block may better explain methadone’s arrhythmia risk beyond I Kr inhibition alone. Drug‐induced augmentation of U waves may represent evidence of blockade of multiple repolarizing ion channels, and evaluation of the effect of that agent on I K1 may be warranted.
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美沙酮阻断心脏向内整流K+电流增加膜不稳定性并放大表面心电图上的U波:一项转化研究
背景美沙酮与猝死和室性心动过速的不成比例的风险相关,尽管延迟整流K+电流(I Kr)只有适度的抑制作用,这是药物相关性心律失常的主要机制。先天性内向整流K+电流(I K1)缺陷与ECG上U波振幅增加和致命性心律失常有关。我们假设美沙酮也可能是ik1的有效抑制剂,有助于延迟复极化,并在表面心电图上表现为增强的U波积分。方法和结果在全细胞电压钳下,美沙酮对重组I K1和原生I K1均有抑制作用,半数最大抑制浓度IC50为1.5 μmol/L,与对I Kr阻滞的半数最大抑制浓度IC50相似(2.9 μmol/L)。美沙酮适度地增加了90%复极时的动作电位持续时间,并减缓了低浓度的末端复极。在较高浓度下,90%复极延长时的动作电位持续时间被消除,但其对终末复极的影响稳步上升,并与舒张膜电位波动增加相关。同时,对美沙酮治疗前后患者的心电图进行了分析,68%的患者与预美沙酮相比U波积分明显增加(导联V3;平均+38%±15%,P=0.016), QT和TPeak至TEnd间隔增加,可能反映了I - Kr阻滞。结论美沙酮是一种有效的I K1抑制剂,可引起体表心电图U波增强。我们认为,ik1阻断导致的膜不稳定性增加可能更好地解释美沙酮的心律失常风险,而不仅仅是ik1抑制。药物诱导的U波增强可能是阻断多个复极化离子通道的证据,并且可能有必要评估该药物对I K1的影响。
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