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钠离子通道必须失活才能从失活状态恢复。

Na+ channels must deactivate to recover from inactivation.

作者信息

Kuo C C, Bean B P

机构信息

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Neuron. 1994 Apr;12(4):819-29. doi: 10.1016/0896-6273(94)90335-2.

Abstract

We studied the kinetics of recovery from inactivation of voltage-dependent Na+ channels in rat hippocampal CA1 neurons. Recovery proceeded exponentially after an initial delay and was accompanied by a tiny ionic current. Both the delay and the time constant of recovery became shorter with increasing hyperpolarization. Negative to -170 mV, the rate of recovery saturated at approximately 4 ms-1 (22 degrees C). Recovery from block by the anticonvulsant drug diphenylhydantoin was far slower, but the pattern of voltage dependence was very similar. Our results suggest that, analogous to the coupling between Na+ channel activation and the development of inactivation, recovery from inactivation is coupled to channel deactivation. Such coupling ensures very little "leak" Na+ current during recovery and a highly voltage-sensitive repriming of Na+ channels for the next impulse.

摘要

我们研究了大鼠海马CA1神经元中电压依赖性Na⁺通道失活后的恢复动力学。在初始延迟后,恢复呈指数进行,并伴有微小的离子电流。随着超极化程度的增加,延迟和恢复时间常数均变短。负至 -170 mV时,恢复速率在约4 ms⁻¹(22℃)饱和。抗惊厥药物苯妥英钠阻断后的恢复要慢得多,但电压依赖性模式非常相似。我们的结果表明,类似于Na⁺通道激活与失活发展之间的耦合,失活后的恢复与通道去激活耦合。这种耦合确保了恢复过程中几乎没有“泄漏”的Na⁺电流,以及Na⁺通道对下一个冲动具有高度电压敏感性的再激活。

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