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1
Inactivation of the sodium channel. II. Gating current experiments.钠通道的失活。II. 门控电流实验。
J Gen Physiol. 1977 Nov;70(5):567-90. doi: 10.1085/jgp.70.5.567.
2
Relations between the inactivation of sodium channels and the immobilization of gating charge in frog myelinated nerve.蛙有髓神经中钠通道失活与门控电荷固定之间的关系。
J Physiol. 1980 Feb;299:573-603. doi: 10.1113/jphysiol.1980.sp013143.
3
Batrachotoxin uncouples gating charge immobilization from fast Na inactivation in squid giant axons.蛙毒素可使乌贼巨大轴突中门控电荷固定与快速钠失活解偶联。
Biophys J. 1988 Oct;54(4):719-30. doi: 10.1016/S0006-3495(88)83007-8.
4
Inactivation of the sodium channel. I. Sodium current experiments.钠通道的失活。I. 钠电流实验。
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5
Coupling between charge movement and pore opening in voltage dependent potassium channels.电压依赖性钾通道中电荷移动与孔开放之间的偶联
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6
Gating of the squid sodium channel at positive potentials. I. Macroscopic ionic and gating currents.乌贼钠通道在正电位下的门控。I. 宏观离子电流和门控电流。
Biophys J. 1994 Jun;66(6):1853-63. doi: 10.1016/S0006-3495(94)80979-8.
7
The role of the putative inactivation lid in sodium channel gating current immobilization.假定失活门在钠通道门控电流固定中的作用。
J Gen Physiol. 2000 May;115(5):609-20. doi: 10.1085/jgp.115.5.609.
8
Pyrethroid modifications of the activation and inactivation kinetics of the sodium channels in squid giant axons.鱿鱼巨大轴突中钠通道激活和失活动力学的拟除虫菊酯修饰
Brain Res. 1990 Mar 26;512(1):26-32. doi: 10.1016/0006-8993(90)91165-d.
9
Charge immobilization of the voltage sensor in domain IV is independent of sodium current inactivation.结构域IV中电压传感器的电荷固定与钠电流失活无关。
J Physiol. 2005 Feb 15;563(Pt 1):83-93. doi: 10.1113/jphysiol.2004.077644. Epub 2004 Dec 2.
10
Destruction of sodium conductance inactivation in squid axons perfused with pronase.用链霉蛋白酶灌注的鱿鱼轴突中钠电导失活的破坏。
J Gen Physiol. 1973 Oct;62(4):375-91. doi: 10.1085/jgp.62.4.375.

引用本文的文献

1
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Molecular Basis of Sodium Channel Inactivation.钠通道失活的分子基础。
bioRxiv. 2025 May 23:2025.05.22.655422. doi: 10.1101/2025.05.22.655422.
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Using metaphorical considerations to benefit research on the sodium channel fast inactivation mechanism.运用隐喻思维助力钠通道快速失活机制的研究。
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Closed State Structure of the Pore Revealed by Uncoupled Shaker K+ Channel.解偶联的振子型钾通道揭示的孔道关闭状态结构
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The crucial decade that ion channels were proven to exist : The vision of Bertil Hille and Clay Armstrong and how it came through.离子通道被证明存在的关键十年:贝蒂尔·希勒和克莱·阿姆斯特朗的远见及其实现过程。
Pflugers Arch. 2025 Apr 22. doi: 10.1007/s00424-025-03085-5.
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Closed State Structure of the Pore Revealed by Uncoupled Shaker K Channel.非偶联型振子钾通道揭示的孔道关闭状态结构
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10
A sodium channel mutant removes fast inactivation with the inactivation particle bound.钠离子通道突变体与失活粒子结合时消除快速失活。
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本文引用的文献

1
The dual effect of membrane potential on sodium conductance in the giant axon of Loligo.枪乌贼巨大轴突中膜电位对钠电导的双重作用。
J Physiol. 1952 Apr;116(4):497-506. doi: 10.1113/jphysiol.1952.sp004719.
2
The action of calcium on the electrical properties of squid axons.钙对鱿鱼轴突电特性的作用。
J Physiol. 1957 Jul 11;137(2):218-44. doi: 10.1113/jphysiol.1957.sp005808.
3
A quantitative description of membrane current and its application to conduction and excitation in nerve.膜电流的定量描述及其在神经传导和兴奋中的应用。
J Physiol. 1952 Aug;117(4):500-44. doi: 10.1113/jphysiol.1952.sp004764.
4
Evidence for two types of sodium conductance in axons perfused with sodium fluoride solution.在灌注氟化钠溶液的轴突中存在两种钠电导的证据。
J Physiol. 1970 Dec;211(3):653-78. doi: 10.1113/jphysiol.1970.sp009298.
5
Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons.四乙铵离子衍生物与巨轴突钾通道的相互作用。
J Gen Physiol. 1971 Oct;58(4):413-37. doi: 10.1085/jgp.58.4.413.
6
Ionic channels in nerve membranes.神经膜中的离子通道。
Prog Biophys Mol Biol. 1970;21:1-32. doi: 10.1016/0079-6107(70)90022-2.
7
Charge movement associated with the opening and closing of the activation gates of the Na channels.与钠通道激活门的开启和关闭相关的电荷移动。
J Gen Physiol. 1974 May;63(5):533-52. doi: 10.1085/jgp.63.5.533.
8
Gating currents of the sodium channels: three ways to block them.钠通道的门控电流:三种阻断方式。
Science. 1974 Feb 22;183(4126):753-4. doi: 10.1126/science.183.4126.753.
9
Ionic pores, gates, and gating currents.离子孔道、门控通道和门控电流。
Q Rev Biophys. 1974 May;7(2):179-210. doi: 10.1017/s0033583500001402.
10
Kinetics and steady-state properties of the charged system controlling sodium conductance in the squid giant axon.控制乌贼巨大轴突中钠电导的带电系统的动力学和稳态特性。
J Physiol. 1974 Jun;239(2):393-434. doi: 10.1113/jphysiol.1974.sp010575.

钠通道的失活。II. 门控电流实验。

Inactivation of the sodium channel. II. Gating current experiments.

作者信息

Armstrong C M, Bezanilla F

出版信息

J Gen Physiol. 1977 Nov;70(5):567-90. doi: 10.1085/jgp.70.5.567.

DOI:10.1085/jgp.70.5.567
PMID:591912
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2228472/
Abstract

Gating current (Ig) has been studied in relation to inactivation of Na channels. No component of Ig has the time course of inactivation; apparently little or no charge movement is associated with this step. Inactivation nonetheless affects Ig by immobilizing about two-thirds of gating charge. Immobilization can be followed by measuring ON charge movement during a pulse and comparing it to OFF charge after the pulse. The OFF:ON ratio is near 1 for a pulse so short that no inactivation occurs, and the ratio drops to about one-third with a time course that parallels inactivation. Other correlations between inactivation and immobilization are that: (a) they have the same voltage dependence; (b) charge movement recovers with the time coures of recovery from inactivation. We interpret this to mean that the immobilized charge returns slowly to "off" position with the time course of recovery from inactivation, and that the small current generated is lost in base-line noise. At -150 mV recover is very rapid, and the immobilized charge forms a distinct slow component of current as it returns to off position. After destruction of inactivation by pronase, there is no immobilization of charge. A model is presented in which inactivation gains its voltage dependence by coupling to the activation gate.

摘要

门控电流(Ig)已被研究与钠通道失活的关系。Ig的任何成分都没有失活的时间进程;显然,这一步骤几乎没有电荷移动或没有电荷移动。然而,失活通过固定约三分之二的门控电荷来影响Ig。固定化可以通过测量脉冲期间的开启电荷移动并将其与脉冲后的关闭电荷进行比较来跟踪。对于短到不会发生失活的脉冲,关闭:开启比率接近1,并且该比率随着与失活平行的时间进程下降到约三分之一。失活与固定化之间的其他相关性在于:(a)它们具有相同的电压依赖性;(b)电荷移动随着从失活恢复的时间进程而恢复。我们将此解释为意味着固定化电荷随着从失活恢复的时间进程缓慢回到“关闭”位置,并且产生的小电流在基线噪声中丢失。在-150 mV时恢复非常迅速,并且固定化电荷在回到关闭位置时形成明显的缓慢电流成分。在胰蛋白酶破坏失活后,没有电荷的固定化。提出了一个模型,其中失活通过与激活门耦合而获得其电压依赖性。