Nitric oxide enhances slow inactivation of voltage-dependent sodium currents in rat nodose neurons

被引:30
作者
Bielefeldt, K [1 ]
Whiteis, CA
Chapleau, MW
Abboud, FM
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Vet Affairs Med Ctr, Iowa City, IA 52242 USA
关键词
nitric oxide; nodose neurons; slow inactivation; sodium currents; modulation;
D O I
10.1016/S0304-3940(99)00553-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nitric oxide (NO) can alter neuronal excitability by decreasing the current through voltage-sensitive sodium channels. We hypothesized that NO inhibits sodium currents in part by promoting slow inactivation. We performed whole-cell voltage clamp experiments on sensory neurons from the nodose ganglion. The voltage-dependence of inactivation was determined after stepping the neurons to various potentials between -100 and 30 mV for 200 ms (fast inactivation) and 3 min (slow inactivation) prior to depolarization to 10 mV. NO shifted the voltage of half-inactivation for fast and slow inactivation to more hyperpolarized potentials by 7 and 12 mV, respectively. Sodium currents exhibited a more profound closed state and slow inactivation after exposure to NO. These results demonstrate for the fist time that the slow inactivation of sodium currents is subject to modulation. Due to its effects on fast and slow inactivation, NO may cause a prolonged decrease in neuronal excitability. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:159 / 162
页数:4
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