Yakehiro M, Seyama I, Narahashi T
Department of Physiology, School of Medicine, Hiroshima University, 1-2-3 Kasumi, Hiroshima 734, Japan.
Pflugers Arch. 1997 Feb;433(4):403-12.
Kinetics of modification of the sodium channel by alpha-dihydrograyanotoxin II (GTX) were studied with voltage-clamped squid giant axons. GTX modified the channel to generate sustained inward current, only when the membrane was kept depolarized to levels more positive than -80mV, in a voltage-dependent manner, increasing the depolarization. Repetitive depolarizing pulses suppressed rather than increased the degree of GTX-evoked modification. GTX-evoked modification proceeded with a dual exponential time course, regardless of the presence or absence of the inactivation gate, but the elimination by pronase of the inactivation gate accelerated GTX-evoked modification. GTX unbound from the sodium channel with a time constant of 30 s at -150 mV in a manner independent of the concentration. The effective concentration that produced a half-maximal sustained sodium current (EC50), which represents GTX-modified channel activity, was estimated to be about 10 microM with one-to-one stoichiometry. The activation/voltage relationship for the sustained sodium current was shifted in the hyperpolarizing direction by as much as 63-94 mV compared with that of peak sodium current. At a GTX concentration of 100 microM and at +20mV, 64% of the sodium channel population was modified. A kinetics model is proposed to account for the behavior of GTX -modified sodium channels.
用电压钳制的枪乌贼巨大轴突研究了α-二氢灰毒素II(GTX)对钠通道的修饰动力学。只有当膜保持去极化至比-80mV更正的水平时,GTX才以电压依赖性方式修饰通道以产生持续内向电流,增加去极化。重复的去极化脉冲抑制而不是增加GTX诱发的修饰程度。无论失活门是否存在,GTX诱发的修饰都以双指数时间进程进行,但用链霉蛋白酶消除失活门会加速GTX诱发的修饰。GTX在-150mV时以与浓度无关的方式从钠通道上解离,时间常数为30s。产生半最大持续钠电流(EC50)的有效浓度(代表GTX修饰的通道活性)估计约为10μM,化学计量比为1:1。与峰值钠电流相比,持续钠电流的激活/电压关系在超极化方向上移动了63-94mV。在100μM的GTX浓度和+20mV时,64%的钠通道群体被修饰。提出了一个动力学模型来解释GTX修饰的钠通道的行为。