Carnevale N T, Wachtel H
Brain Res. 1980 May;203(1):45-65. doi: 10.1016/0165-0173(80)90003-x.
The mechanisms of the slow oscillatory potential in burst firing neurons in the abdominal ganglion of Aplysia californica (L3-L6 and R15) were studied using voltage clamp methods, including a novel tract and hold technique. The steady-state negative resistance characteristic (NRC) of these neurons is attributed to the activation of a moderately fast, persistent, inward current over a range of membrane potential below spike threshold. This inward current is quite sensitive to changes in external sodium concentration (Na)0 and insensitive to potassium (K)0. By contrast, the portion of the I-V curve below the NRC range is insensitive to (Na)0, but highly sensitive to (K)0. The results of 'track and store' voltage clamping show that there are actually two reciprocating currents whose combined action produces the slow oscillation. In addition to the inward current, there is a slow outward current which develops during the depolarized (burst) phase. The slow outward current can also be evoked, and more completely examined, with prolonged depolarizing voltage commands. The extremely slow decay of this current (tau approximately 45 sec) appears to be the factor underlying the slow, ramplike depolarization of Vm during the interburst interval. This slow outward current is insensitive to changes of (Na)0, but changes with (K)0 in a manner consistent with the Nerst equation. We conclude that the burst-inducing slow oscillations are generated as follows: a moderately fast inward sodium dependent current (INa) produces a regenerative depolarization, and this in turn, produces a much slower outward potassium current (IS) which hyperpolarizes the cell. The cycle is completed when IS has decayed sufficiently to allow Vm to depolarize enough to reactivate INa. We have used a quantitative version of this model to determine the time courses of gNa and gK throughout the oscillation, and to explain why different portions of the oscillatory cycle display 'graded' or 'all-or-none' behavior.
利用电压钳技术,包括一种新颖的跟踪与保持技术,研究了加州海兔腹神经节(L3 - L6和R15)爆发式放电神经元中慢振荡电位的机制。这些神经元的稳态负电阻特性(NRC)归因于在低于动作电位阈值的一系列膜电位范围内,一种适度快速、持续的内向电流的激活。这种内向电流对细胞外钠浓度(Na)0的变化非常敏感,而对钾(K)0不敏感。相比之下,I - V曲线在NRC范围以下的部分对(Na)0不敏感,但对(K)0高度敏感。“跟踪与存储”电压钳的结果表明,实际上存在两种往复电流,它们的共同作用产生了慢振荡。除了内向电流外,在去极化(爆发)阶段还会产生一种缓慢的外向电流。通过延长去极化电压指令,也可以诱发并更全面地检测这种缓慢的外向电流。这种电流极其缓慢的衰减(时间常数约为45秒)似乎是爆发间期Vm缓慢、斜坡状去极化的基础。这种缓慢的外向电流对(Na)0的变化不敏感,但随(K)0的变化符合能斯特方程。我们得出结论,诱发爆发的慢振荡是这样产生的:一种适度快速的内向钠依赖性电流(INa)产生再生性去极化,进而产生一种更慢的外向钾电流(IS),使细胞超极化。当IS充分衰减,使Vm去极化到足以重新激活INa时,循环完成。我们使用了该模型的定量版本来确定整个振荡过程中gNa和gK的时间进程,并解释振荡周期的不同部分为何表现出“分级”或“全或无”行为。