Mercuri N B, Bonci A, Calabresi P, Stefani A, Bernardi G
Clinica Neurologica, University of Tor Vergata-Rome, Italy.
Eur J Neurosci. 1995 Mar 1;7(3):462-9. doi: 10.1111/j.1460-9568.1995.tb00342.x.
Intracellular electrophysiological recordings in current- and voltage-clamp mode were obtained from dopaminergic neurons of the rat mesencephalon in an in vitro slice preparation. In current-clamp mode, a time-dependent anomalous rectification (TDR) of the membrane was observed in response to hyperpolarizing current pulses. In single-electrode voltage-clamp mode, a slowly developing inward current (Ih) underlying the TDR was studied by hyperpolarizing voltage commands from a holding potential of -50 to -60 mV. Ih started to be activated at approximately -69 mV, was fully activated at -129 to -141 mV, with half-maximal activation at -87 mV, and showed no inactivation with time. The time course of development of Ih followed a single exponential, and its time constant was voltage-dependent. At -81 mV, Ih activated with a time constant of 379 +/- 47.6 ms, whereas at -129 mV Ih activated with a time constant of 65 +/- 2.2 ms. Its estimated reversal potential was -35 +/- 4 mV. Raising the extracellular concentration of K+ from 2.5 to 6.5 and to 12.5 mM increased the amplitude of Ih while reducing the extracellular concentration of Na+ from 153.2 to 27.2 mM caused a reduction in amplitude of Ih. Bath application of caesium (1-5 mM) reversibly reduced or blocked the TDR/Ih. Perfusion of tetrodotoxin (0.5-1 microM), tetraethylammonium (10-20 mM) or barium (0.3-2 mM) did not significantly affect Ih. Ih was also present in cells impaled with CsCl-filled electrodes.(ABSTRACT TRUNCATED AT 250 WORDS)
在体外脑片制备中,采用电流钳和电压钳模式,对大鼠中脑多巴胺能神经元进行细胞内电生理记录。在电流钳模式下,对超极化电流脉冲的反应中观察到膜的时间依赖性反常整流(TDR)。在单电极电压钳模式下,通过从 -50 至 -60 mV 的钳制电位进行超极化电压指令,研究了TDR 背后缓慢发展的内向电流(Ih)。Ih 在约 -69 mV 开始激活,在 -129 至 -141 mV 完全激活,半数最大激活在 -87 mV,且不随时间失活。Ih 的发展时间进程遵循单指数规律,其时间常数与电压有关。在 -81 mV 时,Ih 以 379±47.6 ms 的时间常数激活,而在 -129 mV 时,Ih 以 65±2.2 ms 的时间常数激活。其估计的反转电位为 -35±4 mV。将细胞外 K⁺浓度从 2.5 mM 提高到 6.5 mM 和 12.5 mM 会增加 Ih 的幅度,而将细胞外 Na⁺浓度从 153.2 mM 降低到 27.2 mM 会导致 Ih 幅度降低。浴用铯(1 - 5 mM)可逆地降低或阻断 TDR/Ih。灌注河豚毒素(0.5 - 1 μM)、四乙铵(10 - 20 mM)或钡(0.3 - 2 mM)对 Ih 无显著影响。用 CsCl 填充电极刺入的细胞中也存在 Ih。(摘要截短于250字)