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利多卡因对完整新生心脏希氏-浦肯野传导的频率依赖性效应——N-乙酰普鲁卡因胺的特性及增强作用

Rate-dependent effects of lidocaine on His-Purkinje conduction in the intact neonatal heart--characterization and amplification by N-acetylprocainamide.

作者信息

Dise T L, Stolfi A, Clarkson C W, Pickoff A S

机构信息

Department of Pediatrics, Tulane University School of Medicine, New Orleans, Louisiana.

出版信息

J Pharmacol Exp Ther. 1991 Nov;259(2):535-42.

PMID:1719192
Abstract

According to mathematical models of antiarrhythmic drug-receptor interactions, lidocaine binds preferentially to the sodium channel when the membrane is depolarized (i.e., the "inactivated" channel state). Therefore, the effect of lidocaine on conduction should be greater when the action potential duration is prolonged. To test this prediction in vivo we evaluated the rate-dependent effects of lidocaine on His-Purkinje conduction in the intact newborn canine heart. Lidocaine's effect was assessed alone and then when given in combination with N-acetylprocainamide, a Class III antiarrhythmic agent. Utilizing intracardiac electrical stimulation and electrogram recording techniques, changes in the steady-state His-Purkinje conduction time during atrial pacing at increasingly rapid cycle lengths, changes in the conduction time of pacing trains delivered directly to the His bundle and changes in conduction time during His bundle extra stimulation were measured. After bilateral sectioning of the vagi and the administration of propranolol (1.0 mg/kg i.v.), His-Purkinje conduction was assessed in newborn canines (ages 5-15 days) under the following conditions: 1) control (n = 18); 2) after an i.v. infusion of lidocaine HCl (serum concentration 3.7 +/- 0.8 micrograms/ml) (n = 12); and 3) after the combined administration of lidocaine and N-acetylprocainamide (serum concentration, 26.4 +/- 6.3 micrograms/ml) (n = 12). Rate-dependent changes in His-Purkinje conduction time were observed in the newborn in response to lidocaine at rapid paced cycle lengths. These changes were significantly amplified by the coadministration of N-acetylprocainamide. Furthermore, the time constant of recovery from rate-dependent conduction delay, determined during His bundle extra stimulation, was 45 msec, which is notably shorter than values reported for lidocaine in the adult.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

根据抗心律失常药物 - 受体相互作用的数学模型,当细胞膜去极化时(即“失活”通道状态),利多卡因优先与钠通道结合。因此,当动作电位持续时间延长时,利多卡因对传导的影响应该更大。为了在体内验证这一预测,我们评估了利多卡因对完整新生犬心脏希氏 - 浦肯野传导的频率依赖性效应。单独评估了利多卡因的作用,然后将其与Ⅲ类抗心律失常药物N - 乙酰普鲁卡因胺联合使用时的作用进行了评估。利用心内电刺激和心电图记录技术,测量了在心房起搏周期长度逐渐加快时希氏 - 浦肯野稳态传导时间的变化、直接施加到希氏束的起搏序列传导时间的变化以及希氏束额外刺激期间的传导时间变化。在双侧切断迷走神经并静脉注射普萘洛尔(1.0 mg/kg)后,在以下条件下评估新生犬(5 - 15日龄)的希氏 - 浦肯野传导:1)对照(n = 18);2)静脉输注盐酸利多卡因后(血清浓度3.7±0.8微克/毫升)(n = 12);3)利多卡因与N - 乙酰普鲁卡因胺联合给药后(血清浓度,26.4±6.3微克/毫升)(n = 12)。在新生犬中观察到,在快速起搏周期长度下,利多卡因会引起希氏 - 浦肯野传导时间的频率依赖性变化。N - 乙酰普鲁卡因胺的联合给药显著放大了这些变化。此外,在希氏束额外刺激期间测定的频率依赖性传导延迟恢复的时间常数为45毫秒,这明显短于在成犬中报道的利多卡因的值。(摘要截短于250字)

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