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大鼠海马锥体细胞中持续时间中等的后超极化。

An after-hyperpolarization of medium duration 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, Stony Brook 11794.

出版信息

J Physiol. 1989 Feb;409:171-90. doi: 10.1113/jphysiol.1989.sp017491.

Abstract
  1. In hippocampal pyramidal cells, action potentials are followed by three after-hyperpolarizations (AHPs): a fast AHP (fAHP) lasting 2-5 ms, a medium AHP (mAHP) lasting 50-100 ms, and a slow AHP (sAHP) lasting more than 1 s. The mechanism underlying the mAHP was studied in CA1 cells (n = 46) in rat hippocampal slices, using injection of depolarizing current to elicit discharge. 2. The current underlying the mAHP was studied by single-electrode voltage clamp in two ways. Either the voltage clamp was activated following a burst of spikes, thus recording the early tail current underlying the mAHP (hybrid clamp), or, after blocking the spikes with tetrodotoxin, the early tail current following a depolarizing voltage clamp command (to -20 to -45 mV for 100-400 ms) was measured. In both cases, the early tail current (measured at -60 mV) showed the following characteristics: (a) it decayed exponentially with a time constant of about 50 ms; (b) it was substantially reduced by the muscarinic agonist carbachol (40-50 microM); (c) it was moderately reduced (by 20% or less) by Ca2+-free medium and Ca2+ channel blockers (Cd2+, Mn2+), which abolished the fAHP and the sAHP; (d) it was partly blocked by tetraethylammonium (TEA, 1-10 mM) both before and during Ca2+ channel blockade; (e) it was resistant to noradrenaline (5-10 microM), which blocked the sAHP, and to apamin (100 nM). 3. The mAHP itself, recorded under current clamp, showed properties corresponding to those of the early tail current. 4. Unlike the current underlying the sAHP, which was reduced and reversed by hyperpolarization, the early tail current appeared to be reduced only at potentials down to -80 mV, and to increase at more negative potentials. The early tail current and mAHP-like undershoot at hyperpolarized potentials was blocked by external Cs+, but not by carbachol, in contrast to the early tail current and mAHP at -60 mV. 5. It was concluded that two currents contribute to the mAHP: IM (a voltage-gated muscarine-sensitive K+ current) and IC (a Ca2+-dependent TEA-sensitive K+ current). TEA reduced both the IM (5 mM) and the IC (1 mM) component of the mAHP. When the cell is hyperpolarized, a third current, IQ (a Ca+-sensitive mixed Na+-K+ inward current activated by hyperpolarization), masks the reversal of the mAHP by causing a depolarizing sag which resembles the decay of the mAHP.
摘要
  1. 在海马锥体细胞中,动作电位之后会出现三种超极化后电位(AHPs):持续2 - 5毫秒的快速超极化后电位(fAHP)、持续50 - 100毫秒的中等超极化后电位(mAHP)以及持续超过1秒的慢速超极化后电位(sAHP)。在大鼠海马切片的CA1细胞(n = 46)中,通过注入去极化电流引发放电,研究了mAHP的潜在机制。2. 通过单电极电压钳以两种方式研究了mAHP的基础电流。要么在一串动作电位之后激活电压钳,从而记录mAHP基础的早期尾电流(混合钳),要么在用河豚毒素阻断动作电位之后,测量去极化电压钳指令(至 - 20至 - 45毫伏,持续100 - 400毫秒)后的早期尾电流。在这两种情况下,早期尾电流(在 - 60毫伏处测量)表现出以下特征:(a)它以约50毫秒的时间常数呈指数衰减;(b)它被毒蕈碱激动剂卡巴胆碱(40 - 50微摩尔)显著降低;(c)它被无钙培养基和钙通道阻滞剂(Cd2 +、Mn2 +)适度降低(降低20%或更少),这些试剂消除了fAHP和sAHP;(d)在钙通道阻断之前和期间,它都被四乙铵(TEA,1 - 10毫摩尔)部分阻断;(e)它对去甲肾上腺素(5 - 10微摩尔)有抗性,去甲肾上腺素阻断sAHP,对蜂毒明肽(100纳摩尔)也有抗性。3. 在电流钳下记录的mAHP本身表现出与早期尾电流相对应的特性。4. 与sAHP的基础电流不同,sAHP的基础电流会因超极化而降低和反转,早期尾电流似乎仅在电位降至 - 80毫伏时降低,而在更负的电位时增加。与在 - 60毫伏处的早期尾电流和mAHP不同,超极化电位下的早期尾电流和类似mAHP的负后电位被外部Cs +阻断,但不被卡巴胆碱阻断。5. 得出的结论是,两种电流对mAHP有贡献:IM(一种电压门控的毒蕈碱敏感钾电流)和IC(一种钙依赖性的TEA敏感钾电流)。TEA降低了mAHP的IM(5毫摩尔)和IC(1毫摩尔)成分。当细胞超极化时,第三种电流IQ(一种由超极化激活的钙敏感混合钠钾内向电流)通过引起类似于mAHP衰减的去极化下陷来掩盖mAHP的反转。

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