Adams W B, Levitan I B
J Physiol. 1985 Mar;360:69-93. doi: 10.1113/jphysiol.1985.sp015604.
The previous paper described a slow depolarizing tail current, ID, and a slow hyperpolarizing tail current, IH, that are activated by action potentials and by brief depolarizing pulses in Aplysia neurone R15. ID and IH are necessary for the generation of bursting pace-maker activity in this cell. In this paper, the voltage and ion dependence of ID and IH are studied in an effort to determine the charge carriers for the two currents. When the slow currents are activated by brief depolarizing pulses delivered under voltage clamp in normal medium, an increase in the size of the pulse of 5-10 mV is usually sufficient to bring about full activation of ID. The apparent threshold in normal medium is approximately -20 mV. In medium in which K+ channels are blocked, full activation of an inward tail current that resembles ID requires increasing the pulse amplitude by only 1-2 mV. In contrast, IH is activated in a graded fashion over a 40 mV range of pulse amplitudes. After activating the currents with action potentials or with supramaximal pulses, ID remains an inward current and IH an outward current over a range of membrane potentials spanning -20 to -120 mV. In normal medium, ID is dependent on both extracellular Na+ concentration ( [Na+]o) and extracellular Ca2+ concentration ( [Ca2+]o). When K+ channels are blocked, ID can be supported by either [Na+]o or [Ca2+]o. IH depends only on [Ca2+]o as long as [Na+]o is at least 50 mM. Neither ID nor IH is decreased by decreasing the K+ gradient or by application of K+ channel blockers. These treatments increase somewhat the apparent amplitude of ID, probably by unmasking it from the large K+ tail current that follows the depolarizing pulse. A direct comparison in the same cell of the tetraethylammonium sensitivity of IH and of the Ca2+-activated K+ current demonstrates that these two currents flow through separate and distinct populations of channels. We conclude that in R15, ID arises in response to the triggering of an axonal action potential which in turn, through an as yet unknown mechanism, causes an increased influx of Na+ and/or Ca2+. We conclude that the apparent outward current IH, which is responsible for the interburst hyperpolarization in a normally bursting R15, in fact arises from a decrease in a resting inward Ca2+ current, possibly as the result of Ca2+-induced inactivation of Ca2+ channels.
上一篇论文描述了一种缓慢去极化尾电流(I_D)和一种缓慢超极化尾电流(I_H),它们由动作电位和海兔神经元R15中的短暂去极化脉冲激活。(I_D)和(I_H)是该细胞产生爆发性起搏活动所必需的。在本文中,研究了(I_D)和(I_H)的电压和离子依赖性,以确定这两种电流的电荷载体。当在正常介质中电压钳制下通过短暂去极化脉冲激活缓慢电流时,脉冲幅度增加5 - 10 mV通常足以使(I_D)完全激活。正常介质中的表观阈值约为 - 20 mV。在钾通道被阻断的介质中,类似于(I_D)的内向尾电流完全激活仅需将脉冲幅度增加1 - 2 mV。相比之下,(I_H)在40 mV的脉冲幅度范围内以分级方式激活。在用动作电位或超最大脉冲激活电流后,在 - 20至 - 120 mV的膜电位范围内,(I_D)仍然是内向电流,(I_H)仍然是外向电流。在正常介质中,(I_D)依赖于细胞外钠离子浓度([Na^+]_o)和细胞外钙离子浓度([Ca^{2 +}]_o)。当钾通道被阻断时,([Na^+]_o)或([Ca^{2 +}]_o)均可支持(I_D)。只要([Na^+]_o)至少为50 mM,(I_H)仅依赖于([Ca^{2 +}]_o)。降低钾离子梯度或应用钾通道阻滞剂均不会使(I_D)或(I_H)减小。这些处理可能通过从去极化脉冲后的大钾尾电流中揭示(I_D),从而在一定程度上增加了(I_D)的表观幅度。在同一细胞中对(I_H)和钙激活钾电流的四乙铵敏感性进行直接比较表明,这两种电流通过不同且独立的通道群体流动。我们得出结论,在R15中,(I_D)是响应轴突动作电位的触发而产生的,而轴突动作电位又通过一种未知机制导致钠离子和/或钙离子内流增加。我们得出结论,在正常爆发的R15中负责爆发间期超极化的表观外向电流(I_H),实际上是由静息内向钙电流的减少引起的,这可能是钙通道钙诱导失活的结果。