Two mutations in the IV/S4-S5 segment of the human skeletal muscle Na+ channel disrupt fast and enhance slow inactivation

被引:15
作者
Alekov, AK
Peter, WG
Mitrovic, N
Lehmann-Horn, F
Lerche, H
机构
[1] Univ Ulm, Dept Appl Physiol, D-89069 Ulm, Germany
[2] Univ Ulm, Dept Neurol, D-89069 Ulm, Germany
关键词
ion channel; patch clamp; myotonia; paralysis;
D O I
10.1016/S0304-3940(01)01895-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Fast and slow inactivation (FI, SI) of the voltage-gated Na+ channel are two kinetically distinct and structurally dissociated processes. The voltage sensor IV/S4 and the intracellular IV/S4-S5 loop have been shown to play an important role in FI mediating the coupling between activation and inactivation. Two mutations in IV/S4-S5 of the human muscle Na+ channel, L1482C/A, disrupt FI by inducing a persistent Na+ current, shifting steady-state inactivation in the depolarizing direction and accelerating its recovery. These effects were more pronounced for L1482A. In contrast, SI of L1482C/A channels was enhanced showing a more complete SI and a 3-fold slowing of its recovery. Effects on SI were more pronounced for L1482C. The results indicate an important role of the IV/S4-S5 loop not only in Fl but also in SI of the Na+ channel. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:173 / 176
页数:4
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