Zaborovskaia L D, Khodorov B I
Biull Eksp Biol Med. 1980 May;89(5):578-80.
The blocking action of neo-gilurytmal (NG), a quaternary derivative of aimalin, on sodium channels was studied in the voltage-clamped node of Ranvier. NG exerted no action on the resting membrane unless the repetitive pulsing was turned on. A series of repetitive depolarizing pulses of short duration (5 ms) produced the accumulating "stimulus-dependent" blockade of sodium channels. The rate and degree of the blockade increased with the increasing of pulse voltage even over the potential range where all the sodium channels were open. Recovery from the blockade occurred within several tens of minutes. Unlike the repetitive pulsing, long-lasting (1 s) depolarization of the membrane produced only a slight increase in the blockade of sodium channels. Elimination of sodium inactivation by aconitine prevented the blocking action of NG. The results of the experiments indicate that NG blocks only the open sodium channels with intact inactivation gate.
在电压钳制的郎飞结中研究了阿马林的季铵衍生物新吉鲁尔通(NG)对钠通道的阻断作用。除非开启重复脉冲,否则NG对静息膜无作用。一系列短持续时间(5毫秒)的重复去极化脉冲产生了钠通道的累积“刺激依赖性”阻断。即使在所有钠通道都开放的电位范围内,阻断的速率和程度也随着脉冲电压的增加而增加。阻断作用在几十分钟内恢复。与重复脉冲不同,膜的持久(1秒)去极化仅使钠通道的阻断略有增加。乌头碱消除钠失活可阻止NG的阻断作用。实验结果表明,NG仅阻断具有完整失活门的开放钠通道。