Toib A, Lyakhov V, Marom S
The Bernard Katz Minerva Center for Cell Biophysics, Department of Physiology, Faculty of Medicine, Technion, and The Rappaport Institute for Research in the Medical Sciences, Haifa 31096, Israel.
J Neurosci. 1998 Mar 1;18(5):1893-903. doi: 10.1523/JNEUROSCI.18-05-01893.1998.
NaII and NaIIA channels are the most abundant voltage-gated channels in neonatal and adult cortex, respectively. The relationships between activity and availability for activation of these channels were examined using the Xenopus expression system. The main point of this work is that the time constant (tau) of recovery from the unavailable (inactivated) pool is related to the duration (t) of previous activation by a power law: tau(t) = p . tD, with a scaling power D congruent to 0.8 and 0.5 for NaII and NaIIA, respectively, and p as a constant kinetic setpoint. These relationships extend from tens of milliseconds to several minutes and are intrinsic to the channel protein. Coexpression of beta1 auxiliary subunit, together with the alpha subunit of the NaIIA channel, modulates the constant kinetic setpoint but not the scaling power of the latter. The power law scaling between activity and availability is not a universal property of ion channels; unlike that of voltage-gated sodium channels, the rate of recovery from slow inactivation of the ShakerB channel is virtually insensitive to the duration of previous stimuli. It is suggested that the power law scaling described here can act as a molecular memory mechanism that preserves traces of previous activity, over a wide range of time scales, in the form of modulated reaction rates. This mechanism should be considered when theorizing about the dynamics of threshold and firing patterns of neurons.
NaII和NaIIA通道分别是新生和成年皮质中最丰富的电压门控通道。利用非洲爪蟾表达系统研究了这些通道的活性与激活可用性之间的关系。这项工作的要点是,从不可用(失活)池恢复的时间常数(tau)与先前激活的持续时间(t)通过幂律相关:tau(t)=p·t^D,其中NaII和NaIIA的标度幂D分别约为0.8和0.5,p为恒定的动力学设定点。这些关系从几十毫秒延伸到几分钟,并且是通道蛋白固有的。β1辅助亚基与NaIIA通道的α亚基共表达,可调节后者的恒定动力学设定点,但不调节其标度幂。活性与可用性之间的幂律标度不是离子通道的普遍特性;与电压门控钠通道不同,ShakerB通道从缓慢失活恢复的速率实际上对先前刺激的持续时间不敏感。有人提出,这里描述的幂律标度可以作为一种分子记忆机制,在很宽的时间尺度范围内,以调制反应速率的形式保留先前活动的痕迹。在对神经元阈值和放电模式的动力学进行理论推导时,应考虑这一机制。