M-channel gating and simulation

被引:29
作者
Selyanko, AA [1 ]
Brown, DA [1 ]
机构
[1] UCL, Dept Pharmacol, London WC1E 6BT, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0006-3495(99)76925-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Single potassium M-channels in rat sympathetic neurons have multiple voltage-dependent kinetic components in their activity: short, medium, and long closed times (tau(CS), tau(CM), and tau(CL)) and short and long open times (tau(OS) and tau(OL)). All five components can be detected in cell-attached patches, but only four of them (tau(CS), tau(CM), tau(OS), and tau(OL)) in excised patches (Selyanko and Brown, 1993, J. Physiol. (Lond.). 472:711-724; 1996, Neuron. 16:151-162; 1996, Neuropharmacology. 35:933-947). Analysis of the burst structure of activity recorded from cell-attached and excised inside-out patches showed lit to be consistent with the sequential kinetic scheme C(L) <-> O(S) <-> C(M) <-> O(L) <-> C(S). Using this scheme and experimentally determined kinetic parameters, we successfully simulated the activity of M-channels both under steady-state conditions and during depolarizing voltage steps. Consistent with the characteristic behavior of macroscopic M-current, ensemble currents constructed from simulated M-channels had exponential activation and deactivation, with no delays, when tested in the range between -50 and -20 mV.
引用
收藏
页码:701 / 713
页数:13
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