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Action potential repolarization and a fast after-hyperpolarization in rat hippocampal pyramidal cells.

机译:大鼠海马锥体细胞的动作电位重新极化和快速的超极化后。

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摘要

1. The repolarization of the action potential, and a fast after-hyperpolarization (a.h.p.) were studied in CA1 pyramidal cells (n = 76) in rat hippocampal slices (28-37 degrees C). Single spikes were elicited by brief (1-3 ms) current pulses, at membrane potentials close to rest (-60 to -70 mV). 2. Each action potential was followed by four after-potentials: (a) the fast a.h.p., lasting 2-5 ms; (b) an after-depolarization; (c) a medium a.h.p., (50-100 ms); and (d) a slow a.h.p. (1-2 s). Both the fast a.h.p. and the slow a.h.p. (but not the medium a.h.p.) were inhibited by Ca2+-free medium or Ca2+-channel blockers (Co2+, Mn2+ or Cd2+); but tetraethylammonium (TEA; 0.5-2 nM) blocked only the fast a.h.p., and noradrenaline (2-5 microM) only the slow a.h.p. This suggests that two Ca2+-activated K+ currents were involved: a fast, TEA-sensitive one (IC) underlying the fast a.h.p., and a slow noradrenaline-sensitive one (IAHP) underlying the slow a.h.p. 3. Like the fast a.h.p., spike repolarization seems to depend on a Ca2+-dependent K+ current of the fast, TEA-sensitive kind (IC). The repolarization was slowed by Ca2+-free medium, Co2+, Mn2+, Cd2+, or TEA, but not by noradrenaline. Charybdotoxin (CTX; 30 nM), a scorpion toxin which blocks the large-conductance Ca2+-activated K+ channel in muscle, had a similar effect to TEA. The effects of TEA and Cd2+ (or Mn2+) showed mutual occlusion. Raising the external K+ concentration reduced the fast a.h.p. and slowed the spike repolarization, whereas Cl- loading of the cell was ineffective. 4. The transient K+ current, IA, seems also to contribute to spike repolarization, because: (a) 4-aminopyridine (4-AP; 0.1 mM), which blocks IA, slowed the spike repolarization; (b) depolarizing pre-pulses, which inactivate IA, had a similar effect; (c) hyperpolarizing pre-pulses speeded up the spike repolarization; (d) the effects of 4-AP and pre-pulses persisted during Ca2+ blockade (like IA); and (e) depolarizing pre-pulses reduced the effect of 4-AP. 5. Pre-pulses or 4-AP broadened the spike less, and in a different manner, than Ca2+-free medium, Cd2+, Co2+, Mn2+, TEA or CTX. The former broadening was uniform, with little effect on the fast a.h.p., whereas the latter affected mostly the last two-thirds of the spike repolarization and abolished the fast a.h.p.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.在大鼠海马切片(28-37摄氏度)的CA1锥体细胞(n = 76)中研究了动作电位的重新极化以及超极化后的快速极化(a.h.p.)。短暂的(1-3 ms)电流脉冲在接近于静止状态(-60至-70 mV)的膜电位上引发单个尖峰。 2.每个动作电位后面跟随四个后电位:(a)快速a.h.p.,持续2-5毫秒; (b)去极化后; (c)a.h.p.(50-100毫秒); (d)缓慢的a.h.p. (1-2秒)。两者都是快速的和缓慢的a.h.p. (但不含a.h.p.培养基)被不含Ca2 +的培养基或Ca2 +通道阻滞剂(Co2 +,Mn2 +或Cd2 +)抑制;但四乙铵(TEA; 0.5-2 nM)仅阻止快速a.h.p.,去甲肾上腺素(2-5 microM)仅阻止缓慢a.h.p.这表明涉及到两个Ca2 +激活的K +电流:在快速a.h.p下方有一个快速的,对TEA敏感的电流(IC),在该缓慢a.h.p下方有一个缓慢的去甲肾上腺素敏感的电流(IAHP)。 3.像快速a.h.p.一样,尖峰复极化似乎取决于快速的,对TEA敏感的类型(IC)的Ca2 +依赖性K +电流。不含Ca2 +的培养基,Co2 +,Mn2 +,Cd2 +或TEA可使复极化减慢,但去甲肾上腺素则不能。 Charybdotoxin(CTX; 30 nM)是一种蝎子毒素,可以阻断肌肉中大电导的Ca2 +激活的K +通道,其作用与TEA相似。 TEA和Cd2 +(或Mn2 +)的作用表现为相互咬合。提高外部K +浓度会降低快速a.h.p.并减慢了尖峰的复极化,而细胞的Cl加载是无效的。 4.瞬时K +电流IA似乎也有助于尖峰复极化,因为:(a)阻止IA的4-氨基吡啶(4-AP; 0.1 mM)减慢了尖峰复极化; (b)使IA失活的去极化预脉冲具有相似的作用; (c)超极化预脉冲加快了尖峰再极化; (d)4-AP和预脉冲在Ca2 +阻断期间(如IA)持续存在的影响; (e)去极化预脉冲降低了4-AP的作用。 5.与不含Ca2 +的培养基,Cd2 +,Co2 +,Mn2 +,TEA或CTX相比,预脉冲或4-AP的加宽幅度较小,且以不同的方式加宽了尖峰。前者的增宽是均匀的,对快速a.h.p.几乎没有影响,而后者主要影响了尖峰复极化的最后三分之二并取消了快速a.h.p.(摘要截断了400字)

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