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[利多卡因新型铵衍生物(LKhT - 12 - 02)的抗心律失常作用机制]

[The mechanism of antiarrhythmic action of a new ammonium derivative of lidocaine (LKhT-12-02)].

作者信息

Blinov D S, Balashov V P, Sernov L N, Kazachenko V N, Blinova E V, Belova L A, Astashev M E

出版信息

Eksp Klin Farmakol. 2006 Nov-Dec;69(6):31-3.

Abstract

The results of electrophysiological investigation of the effects of LKhT-12-02 (a quaternary ammonium derivative of lidocaine) on the intact cat heart and the isolated ion channels of Lymnaea stagnalis snail showed that this compound belongs to class 1B antiarrhythmic agents (Vaughan - Williams classification). The drug does not suppress the automatic nonmonotonic rhythm driver, does not influence the conductance in ventricles, auricles, and atrioventricular node in the sinus rhythm, and does not elongate the effective refractory period of the auricles and atrioventricular node. LKhT-12-02 decreases the rate of fast depolarization of the action potential, while not reducing its duration. The compound does not influence the conduction of sodium ion channels.

摘要

对LKhT - 12 - 02(利多卡因的季铵衍生物)对完整猫心脏和椎实螺分离离子通道作用的电生理研究结果表明,该化合物属于1B类抗心律失常药物( Vaughan - Williams分类)。该药物不抑制自动非单调节律驱动,不影响窦性心律时心室、心房和房室结的电导率,也不延长心房和房室结的有效不应期。LKhT - 12 - 02降低动作电位快速去极化的速率,而不缩短其持续时间。该化合物不影响钠离子通道的传导。

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