Watanabe S, Takagi H, Miyasho T, Inoue M, Kirino Y, Kudo Y, Miyakawa H
Faculty of Pharmaceutical Sciences, University of Tokyo, Bunkyo-ku, Tokyo 113, Japan.
Brain Res. 1998 Apr 27;791(1-2):43-55. doi: 10.1016/s0006-8993(98)00048-1.
The distribution and function of voltage-gated Ca2+ channels in Purkinje neurons in rat cerebellar slices were studied using simultaneous Ca2+ imaging and whole-cell patch clamp recording techniques. Voltage-gated Ca2+ channels were activated by applying depolarizing voltage steps through the pipette attached at the soma in a voltage-clamp mode in the presence of tetrodotoxin. Poor space clamp due to extensive arborization of the dendrites allowed the dendrites to fire Ca2+ spikes. Ca2+ imaging with Fura-2 injected through the pipette, showed a steady [Ca2+]i increase at the soma and transient, spike-linked [Ca2+]i jumps in the dendrites. omega-Agatoxin-IVA (200 nM) abolished the depolarization-induced Ca2+ spikes, the spike-linked [Ca2+]i increase in the dendrites, and the steady [Ca2+]i increase at the soma. omega-Conotoxin-GVIA (5 microM) and nifedipine (3 microM) had no significant effect on the depolarization-induced responses. In the presence of 4-aminopyridine(2 mM) and omega-Agatoxin-IVA, transient [Ca2+]i increases remained in the dendrites. Low concentrations of Ni2+(100 microM) reversibly suppressed this [Ca2+]i increase. The voltage for half-maximal activation and inactivation of this component were lower than -50 mV and -31 mV, respectively. In normal conditions, low concentration of Ni2+ slowed the onset of the Ca2+ spike without changing the time course of the spikes or the amplitude of the accompanying [Ca2+]i increase. These results show that omega-Agatoxin-IVA-sensitive Ca2+ channels are distributed both in the soma and the dendrites, and are responsible for dendritic Ca2+ spikes, whereas low-voltage activated, Ni2+-sensitive Ca2+ channels are distributed in the whole dendrites including both thick and fine branches, and provide boosting current for spike generation.
采用同步钙成像和全细胞膜片钳记录技术,研究了大鼠小脑切片浦肯野神经元中电压门控性Ca2+通道的分布和功能。在存在河豚毒素的情况下,通过电压钳模式下连接到胞体的移液管施加去极化电压阶跃来激活电压门控性Ca2+通道。由于树突广泛分支导致空间钳制不佳,使得树突能够产生Ca2+尖峰。通过移液管注入Fura-2进行钙成像,结果显示胞体处[Ca2+]i持续增加,而树突中出现短暂的、与尖峰相关的[Ca2+]i跃升。ω-芋螺毒素-IVA(200 nM)消除了去极化诱导的Ca2+尖峰、树突中与尖峰相关的[Ca2+]i增加以及胞体处[Ca2+]i的持续增加。ω-芋螺毒素-GVIA(5 μM)和硝苯地平(3 μM)对去极化诱导的反应无显著影响。在存在4-氨基吡啶(2 mM)和ω-芋螺毒素-IVA的情况下,树突中仍存在短暂的[Ca2+]i增加。低浓度的Ni2+(100 μM)可逆性抑制这种[Ca2+]i增加。该成分的半数最大激活电压和失活电压分别低于-50 mV和-31 mV。在正常条件下,低浓度的Ni2+减缓了Ca2+尖峰的起始,而不改变尖峰的时间进程或伴随的[Ca2+]i增加幅度。这些结果表明,ω-芋螺毒素-IVA敏感的Ca2+通道分布于胞体和树突中,负责树突Ca2+尖峰的产生;而低电压激活、Ni2+敏感的Ca2+通道分布于包括粗支和细支在内的整个树突中,并为尖峰产生提供增强电流。