Bourque C W, Renaud L P
J Physiol. 1985 Jun;363:429-39. doi: 10.1113/jphysiol.1985.sp015720.
Action potential durations, measured at one-third peak amplitude, were examined during intracellular recordings in 134 supraoptic nucleus neurones maintained in vitro in perfused hypothalamic explants. Spike durations ranged between 1.2 and 3.9 ms and were dependent on firing frequency. Shortest measurements (1.74 +/- 0.03 ms; mean +/- S.E. of mean) were obtained during relative quiescence, i.e. less than or equal to 0.5 Hz. A gradual increase in firing frequency through continuous injection of depolarizing current prolonged spike duration, with maximum levels (2.68 +/- 0.05 ms) achieved at 20 Hz. When interspike interval variability was eliminated and firing was more precisely regulated by brief 15-20 ms intracellular current pulses given at pre-determined frequencies, a proportional relationship between increasing spike duration and firing frequency was retained but the change in spike duration at frequencies between 2 and 10 Hz was less pronounced. Once action potentials had achieved the long duration configuration, their return to the shorter duration took place gradually during any succeeding silent interval with a time constant of 4.9 s. Action potential broadening occurred progressively and was most pronounced at the onset of spontaneous or current-induced bursts. In thirty-six phasically active neurones, spike broadening at the onset of a burst was concurrent with the presence of 5-10 consecutive short (less than or equal to 100 ms) interspike intervals; thereafter, despite a greater than 50% reduction in firing frequency, action potential durations remained prolonged throughout the burst. In all of nineteen cells tested, frequency-dependent changes in spike duration were reversibly decreased or blocked by Cd2+, Co2+ and Mn2+, or when CaCl2 was exchanged for equimolar amounts of EGTA in the perfusion medium. These observations indicate that a Ca2+ conductance contributes to frequency- and firing-pattern-dependent changes in spike duration in rat supraoptic nucleus neurones.
在灌注下丘脑外植体中体外培养的134个视上核神经元进行细胞内记录期间,检测了在动作电位峰值幅度的三分之一处测量的动作电位持续时间。动作电位持续时间在1.2至3.9毫秒之间,并且取决于放电频率。在相对静止状态下,即小于或等于0.5赫兹时,获得最短测量值(1.74±0.03毫秒;平均值±平均值的标准误差)。通过持续注入去极化电流使放电频率逐渐增加,会延长动作电位持续时间,在20赫兹时达到最高水平(2.68±0.05毫秒)。当消除动作电位间期变异性,并通过以预定频率给予短暂的15 - 20毫秒细胞内电流脉冲更精确地调节放电时,动作电位持续时间增加与放电频率之间的比例关系得以保留,但在2至10赫兹频率下动作电位持续时间的变化不太明显。一旦动作电位达到长时程构型,在任何后续的静息期内,它们会以4.9秒的时间常数逐渐恢复到较短的持续时间。动作电位展宽逐渐发生,并且在自发或电流诱发的爆发开始时最为明显。在36个相位活跃的神经元中,爆发开始时的动作电位展宽与存在5 - 10个连续的短(小于或等于100毫秒)动作电位间期同时出现;此后,尽管放电频率降低超过50%,动作电位持续时间在整个爆发过程中仍保持延长。在所有测试的19个细胞中,动作电位持续时间的频率依赖性变化被Cd2 +、Co2 +和Mn2 +可逆地降低或阻断,或者当在灌注培养基中用等摩尔量的EGTA替代CaCl2时也是如此。这些观察结果表明,Ca2 +电导有助于大鼠视上核神经元动作电位持续时间的频率和放电模式依赖性变化。