Department of Psychiatry and Neurosciences, Laval University, Québec, Canada G1V 0A6.
Exp Neurol. 2013 Jul;245:5-14. doi: 10.1016/j.expneurol.2012.12.001. Epub 2012 Dec 19.
Neocortical neurons can be classified in four major electrophysiological types according to their pattern of discharge: regular-spiking (RS), intrinsically-bursting (IB), fast-rhythmic-bursting (FRB), and fast-spiking (FS). Previously, we have shown that these firing patterns are not fixed and can change as a function of membrane potential and states of vigilance. Other studies have reported that extracellular calcium concentration ([Ca(2+)]o) fluctuates as a function of the phase of the cortical slow oscillation. In the present study we investigated how spontaneous and induced changes in [Ca(2+)]o affect the properties of action potentials (APs) and firing patterns in cortical neurons in vivo. Intracellular recordings were performed in cats anesthetized with ketamine-xylazine during spontaneous [Ca(2+)]o fluctuation and while changing [Ca(2+)]o with reverse microdialysis. When [Ca(2+)]o fluctuated spontaneously according to the phase of the slow oscillation, we found an increase of the firing threshold and a decrease of the afterhyperpolarization (AHP) amplitude during the depolarizing (active, up) phase of the slow oscillation and some neurons also changed their firing pattern as compared with the hyperpolarizing (silent, down) phase. Induced changes in [Ca(2+)]o significantly affected the AP properties in all neurons. The AHP amplitude was increased in high calcium conditions and decreased in low calcium conditions, in particular the earliest components. Modulation of spike AHP resulted in notable modulation of intrinsic firing pattern and some RS neurons revealed burst firing when [Ca(2+)]o was decreased. We also found an increase in AHP amplitude in high [Ca(2+)]o with in vitro preparation. We suggest that during spontaneous network oscillations in vivo, the dynamic changes of firing patterns depend partially on fluctuations of the [Ca(2+)]o.
根据放电模式,新皮层神经元可分为 4 种主要的电生理类型:规则放电型(RS)、内在爆发型(IB)、快速节律爆发型(FRB)和快速放电型(FS)。此前,我们已经证明这些放电模式不是固定的,它们可以随着膜电位和警觉状态的变化而改变。其他研究表明,细胞外钙离子浓度 ([Ca(2+)]o) 随皮质慢振荡的相位而波动。在本研究中,我们研究了 [Ca(2+)]o 的自发和诱导变化如何影响体内皮质神经元动作电位 (AP) 和放电模式的特性。在氯胺酮-甲苯噻嗪麻醉的猫中进行了细胞内记录,在此期间,[Ca(2+)]o 根据慢振荡的相位自发波动,并通过反向微透析改变 [Ca(2+)]o。当 [Ca(2+)]o 根据慢振荡的相位自发波动时,我们发现放电阈值在慢振荡的去极化(活跃,上)相增加,后超极化(AHP)幅度降低,与超极化(沉默,下)相相比,一些神经元也改变了它们的放电模式。诱导的 [Ca(2+)]o 变化显著影响所有神经元的 AP 特性。在高钙条件下,AHP 幅度增加,在低钙条件下,特别是早期成分,AHP 幅度减小。AP 后超极化的调制导致内在放电模式的显著调制,当 [Ca(2+)]o 降低时,一些 RS 神经元显示爆发性放电。我们还发现,在高 [Ca(2+)]o 下,体外制备的 AHP 幅度增加。我们认为,在体内自发网络振荡期间,放电模式的动态变化部分取决于 [Ca(2+)]o 的波动。