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大鼠海马锥体神经元动作电位复极化及快速超极化后电位

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

作者信息

Storm J F

机构信息

Department of Neurobiology and Behavior, State University of New York at Stony Brook 11794.

出版信息

J Physiol. 1987 Apr;385:733-59. doi: 10.1113/jphysiol.1987.sp016517.

Abstract
  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)
摘要
  1. 在28 - 37摄氏度的大鼠海马切片中,对CA1锥体神经元(n = 76)动作电位的复极化和快速超极化后电位(a.h.p.)进行了研究。通过短暂(1 - 3毫秒)的电流脉冲,在接近静息电位(-60至-70毫伏)的膜电位下诱发单个峰电位。2. 每个动作电位之后跟随四个后电位:(a)快速a.h.p.,持续2 - 5毫秒;(b)一个去极化后电位;(c)一个中等a.h.p.(50 - 100毫秒);以及(d)一个缓慢a.h.p.(1 - 2秒)。快速a.h.p.和缓慢a.h.p.(但不是中等a.h.p.)在无钙培养基或钙通道阻滞剂(Co2 +、Mn2 +或Cd2 +)作用下受到抑制;但四乙铵(TEA;0.5 - 2纳摩尔)仅阻断快速a.h.p.,去甲肾上腺素(2 - 5微摩尔)仅阻断缓慢a.h.p.。这表明涉及两种钙激活钾电流:一种快速的、对TEA敏感的电流(IC),是快速a.h.p.的基础,以及一种缓慢的、对去甲肾上腺素敏感的电流(IAHP),是缓慢a.h.p.的基础。3. 与快速a.h.p.一样,峰电位复极化似乎依赖于快速的、对TEA敏感的那种钙依赖钾电流(IC)。在无钙培养基、Co2 +、Mn2 +、Cd2 +或TEA作用下,复极化减慢,但去甲肾上腺素无此作用。蝎毒素Charybdotoxin(CTX;30纳摩尔)可阻断肌肉中的大电导钙激活钾通道,其作用与TEA类似。TEA和Cd2 +(或Mn2 +)的作用表现为相互阻断。提高细胞外钾浓度可降低快速a.h.p.并减慢峰电位复极化,而细胞内氯离子负载则无效。4. 瞬时钾电流IA似乎也对峰电位复极化有贡献,因为:(a)阻断IA的4 - 氨基吡啶(4 - AP;0.1毫摩尔)减慢了峰电位复极化;(b)使IA失活的去极化预脉冲有类似作用;(c)超极化预脉冲加快了峰电位复极化;(d)4 - AP和预脉冲的作用在钙阻断期间持续存在(与IA一样);以及(e)去极化预脉冲降低了4 - AP的作用。5.预脉冲或4 - AP使峰电位增宽的程度小于无钙培养基、Cd2 +、Co2 +、Mn2 +、TEA或CTX,且方式不同。前者引起的增宽是均匀的,对快速a.h.p.影响很小,而后者主要影响峰电位复极化的后三分之二并消除快速a.h.p.(摘要截断于400字)

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