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大鼠丘脑神经元中T型Ca2+通道失活后的恢复

Recovery from inactivation of t-type ca2+ channels in rat thalamic neurons.

作者信息

Kuo C C, Yang S

机构信息

Department of Physiology, National Taiwan University College of Medicine, and Department of Neurology, National Taiwan University Hospital, Taipei 100, Taiwan.

出版信息

J Neurosci. 2001 Mar 15;21(6):1884-92. doi: 10.1523/JNEUROSCI.21-06-01884.2001.

Abstract

We studied the gating kinetics, especially the kinetics of recovery from inactivation, of T-type Ca(2+) channels (T-channels) in thalamic neurons. The recovery course is associated with no discernible Ca(2+) current and is characterized by an initial delay, as well as a subsequent exponential phase. These findings are qualitatively similar to previous observations on neuronal Na(+) channels and suggest that T-channels also must deactivate to recover from inactivation. In contrast to Na(+) channels in which both the delay and the time constant of the exponential phase are shortened with increasing hyperpolarization, in T-channels the time constant of the exponential recovery phase remains unchanged between -100 and -200 mV, although the initial delay is still shortened e-fold per 43 mV hyperpolarization over the same voltage range. The deactivating kinetics of tail T-currents also show a similar voltage dependence between -90 and -170 mV. According to the hinged-lid model of fast inactivation, these findings suggest that the affinity difference between inactivating peptide binding to the activated channel and binding to the fully deactivated channel is much smaller in T-channels than in Na(+) channels. Moreover, the inactivating peptide in T-channels seems to have much slower binding and unbinding kinetics, and the unbinding rates probably remain unchanged once the inactivated T-channel has gone through the initial steps of deactivation and "closes" the pore (with the activation gate). T-channels thus might have a more rigid hinge and a more abrupt conformational change in the inactivation machinery associated with opening and closing of the pore.

摘要

我们研究了丘脑神经元中T型钙通道(T通道)的门控动力学,尤其是失活恢复的动力学。恢复过程与可察觉的钙电流无关,其特征是初始延迟以及随后的指数阶段。这些发现与先前对神经元钠通道的观察结果在定性上相似,表明T通道也必须失活才能从失活状态恢复。与钠通道不同,在钠通道中,随着超极化程度的增加,指数阶段的延迟和时间常数都会缩短,而在T通道中,尽管在相同电压范围内每超极化43 mV初始延迟仍会以e倍的速度缩短,但指数恢复阶段的时间常数在-100至-200 mV之间保持不变。尾电流T的失活动力学在-90至-170 mV之间也表现出类似的电压依赖性。根据快速失活的铰链盖模型,这些发现表明,在T通道中,失活肽与激活通道结合和与完全失活通道结合之间的亲和力差异比在钠通道中要小得多。此外,T通道中的失活肽似乎具有慢得多的结合和解离动力学,并且一旦失活的T通道经历了失活的初始步骤并“关闭”孔道(通过激活门),解离速率可能保持不变。因此,T通道可能具有更刚性的铰链以及与孔道打开和关闭相关的失活机制中更突然的构象变化。

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