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2
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3
Human Nav1.6 Channels Generate Larger Resurgent Currents than Human Nav1.1 Channels, but the Navβ4 Peptide Does Not Protect Either Isoform from Use-Dependent Reduction.与人类Nav1.1通道相比,人类Nav1.6通道产生的复苏电流更大,但Navβ4肽并不能保护这两种亚型免受使用依赖性衰减的影响。
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4
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本文引用的文献

1
Evolution of voltage-gated Na(+) channels.电压门控性钠离子通道的进化
J Exp Biol. 2002 Mar;205(Pt 5):575-84. doi: 10.1242/jeb.205.5.575.
2
Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2.导致伴有热性惊厥附加症2型的全身性癫痫的两种电压门控钠通道突变的功能效应
J Neurosci. 2001 Oct 1;21(19):7481-90. doi: 10.1523/JNEUROSCI.21-19-07481.2001.
3
Differential control of clustering of the sodium channels Na(v)1.2 and Na(v)1.6 at developing CNS nodes of Ranvier.发育中的中枢神经系统郎飞结处钠通道Na(v)1.2和Na(v)1.6聚集的差异调控。
Neuron. 2001 Apr;30(1):105-19. doi: 10.1016/s0896-6273(01)00266-5.
4
Compact myelin dictates the differential targeting of two sodium channel isoforms in the same axon.紧密髓鞘决定了同一轴突中两种钠通道亚型的差异靶向。
Neuron. 2001 Apr;30(1):91-104. doi: 10.1016/s0896-6273(01)00265-3.
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Resurgence of sodium channel research.钠通道研究的复兴
Annu Rev Physiol. 2001;63:871-94. doi: 10.1146/annurev.physiol.63.1.871.
6
Nomenclature of voltage-gated sodium channels.电压门控钠通道的命名法。
Neuron. 2000 Nov;28(2):365-8. doi: 10.1016/s0896-6273(00)00116-1.
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From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels.从离子电流到分子机制:电压门控钠通道的结构与功能
Neuron. 2000 Apr;26(1):13-25. doi: 10.1016/s0896-6273(00)81133-2.
8
Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses.钠通道Na(v)1.6定位于郎飞氏结、树突和突触处。
Proc Natl Acad Sci U S A. 2000 May 9;97(10):5616-20. doi: 10.1073/pnas.090034797.
9
Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A.人类神经元钠通道基因SCN8A的外显子组织、编码序列、物理图谱及基因内多态性标记
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Functional analysis of the mouse Scn8a sodium channel.小鼠Scn8a钠通道的功能分析
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Nav1.6钠通道的使用依赖性增强

Use-dependent potentiation of the Nav1.6 sodium channel.

作者信息

Zhou W, Goldin A L

机构信息

Department of Microbiology & Molecular Genetics, University of California, Irvine, California 92697-4025, USA.

出版信息

Biophys J. 2004 Dec;87(6):3862-72. doi: 10.1529/biophysj.104.045963. Epub 2004 Oct 1.

DOI:10.1529/biophysj.104.045963
PMID:15465873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1304897/
Abstract

Nav1.2 and Nav1.6 are two voltage-gated sodium channel isoforms that are abundant in the adult central nervous system. These channels are expressed in different cells and localized in different neuronal regions, which may reflect functional specialization. To examine this possibility, we compared the properties of Nav1.2 and Nav1.6 in response to a rapid series of repetitive depolarizations. Currents through Nav1.6 coexpressed with beta1 demonstrated use-dependent potentiation during a rapid train of depolarizations. This potentiation was in contrast to the use-dependent decrease in current for Nav1.2 with beta1. The voltage dependence of potentiation correlated with the voltage dependence of activation, and it still occurred when fast inactivation was removed by mutation. Rapid stimulation accelerated a slow phase of activation in the Nav1.6 channel that had fast inactivation removed, resulting in faster channel activation. Although the Nav1.2 channel with fast inactivation removed also demonstrated slightly faster activation, that channel showed very pronounced slow inactivation compared to Nav1.6. These results indicate that potentiation of Nav1.6 sodium currents results from faster channel activation, and that this effect is masked by slow inactivation in Nav1.2. The data suggest that Nav1.6 might be more resistant to inactivation, which might be helpful for high-frequency firing at nodes of Ranvier compared to Nav1.2.

摘要

Nav1.2和Nav1.6是两种电压门控钠通道亚型,在成体中枢神经系统中大量存在。这些通道在不同细胞中表达,并定位于不同的神经元区域,这可能反映了功能特化。为了检验这种可能性,我们比较了Nav1.2和Nav1.6在快速系列重复去极化反应中的特性。与β1共表达的Nav1.6所介导的电流在快速去极化串刺激期间表现出使用依赖性增强。这种增强与与β1共表达的Nav1.2电流的使用依赖性降低形成对比。增强的电压依赖性与激活的电压依赖性相关,并且当通过突变去除快速失活时仍然发生。快速刺激加速了去除快速失活的Nav1.6通道的缓慢激活相,导致通道激活更快。尽管去除快速失活的Nav1.2通道也表现出稍快的激活,但与Nav1.6相比,该通道表现出非常明显的缓慢失活。这些结果表明,Nav1.6钠电流的增强源于更快的通道激活,并且这种效应在Nav1.2中被缓慢失活所掩盖。数据表明,与Nav1.2相比,Nav1.6可能对失活更具抗性,这可能有助于郎飞结处的高频放电。