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Interactions of aminopyridines with potassium channels of squid axon membranes.

机译:氨基吡啶与鱿鱼轴突膜钾通道的相互作用。

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摘要

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.
机译:使用电压钳和内部灌注技术检查了氨基吡啶对鱿鱼巨轴突膜离子电导的影响。 4-氨基吡啶(4-AP)降低钾电流,但对瞬时钠电流没有影响。 4-AP对钾通道的阻滞作用明显较小,其中(a)强去极化至正膜电位,(b)增加给定去极化步骤的持续时间,以及(c)增加步骤去极化的频率。在高外部钾浓度下进行的实验表明,4-AP的作用与钾离子运动的方向无关。 3-氨基吡啶和2-氨基吡啶与4-AP没有区别,只是效力不同。结论是,氨基嘧啶可用作阻止可兴奋膜中钾电导的工具,但只能在特定的特定电压和频率范围内。

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