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氨基吡啶与鱿鱼轴突膜钾通道的相互作用。

Interactions of aminopyridines with potassium channels of squid axon membranes.

作者信息

Yeh J Z, Oxford G S, Wu C H, Narahashi T

出版信息

Biophys J. 1976 Jan;16(1):77-81. doi: 10.1016/S0006-3495(76)85663-9.

Abstract

The effects of aminopyridines on ionic conductances of the squid giant axon membrane were examined using voltage clamp and internal perfusion techniques. 4-Aminopyridine (4-AP) reduced potassium currents, but had no effect upon transient sodium currents. The block of potassium channels by 4-AP was substantially less with (a) strong depolarization to positive membrane potentials, (b) increasing the duration of a given depolarizing step, and (c) increasing the frequency of step depolarizations. Experiments with high external potassium concentrations revealed that the effect of 4-AP was independent of the direction of potassium ion movement. Both 3- and 2-aminopyridine were indistinguishable from 4-AP except in potency. It is concluded that aminopyrimidines may be used as tools to block the potassium conductance in excitable membranes, but only within certain specific voltage and frequency limits.

摘要

运用电压钳制和内部灌注技术,研究了氨基吡啶对乌贼巨大轴突膜离子电导的影响。4-氨基吡啶(4-AP)可降低钾电流,但对瞬时钠电流无影响。在以下情况下,4-AP对钾通道的阻断作用会显著减弱:(a)将膜电位强力去极化至正值;(b)延长给定去极化步骤的持续时间;(c)增加去极化步骤的频率。高细胞外钾浓度实验表明,4-AP的作用与钾离子移动方向无关。除了效力不同外,3-氨基吡啶和2-氨基吡啶与4-AP的作用并无差异。得出的结论是,氨基嘧啶可用作阻断可兴奋膜中钾电导的工具,但仅在某些特定的电压和频率限制范围内有效。

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