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大鼠新皮层神经元兴奋性突触后电位的电压依赖性

Voltage dependence of excitatory postsynaptic potentials of rat neocortical neurons.

作者信息

Deisz R A, Fortin G, Zieglgänsberger W

机构信息

Clinical Neuropharmacology, Max Planck Institute for Psychiatry, Munich, Federal Republic of Germany.

出版信息

J Neurophysiol. 1991 Feb;65(2):371-82. doi: 10.1152/jn.1991.65.2.371.

Abstract
  1. The properties of excitatory postsynaptic potentials (EPSPs) of rat neocortical neurons were investigated with a fast single-electrode current-voltage clamp in vitro. Typically, apparently pure EPSPs were obtained by selection of electric stimuli of low intensity. 2. The amplitude and time integral of the EPSP increased when the neuron was depolarized. At threshold for generation of action potentials, the amplitude of EPSPs was increased by approximately 30% [from 5.0 +/- 2.1 to 6.3 +/- 1.0 (SD) mV, n = 12]. The integral of EPSPs was maximally about fourfold (3.7 +/- 1.5, n = 16) larger than at resting membrane potential (Em). The mechanisms involved in this augmentation of EPSPs were further investigated. 3. The amplitude and the time integral of excitatory postsynaptic currents (EPSCs) decreased linearly with shifts in command potential from -100 to -60 mV. The decrease of the EPSC integral with depolarization indicates that the enhancement of the EPSP may be brought about by recruitment of a voltage-dependent inward current. 4. Evoking EPSPs at various delays after the onset of small depolarizing current pulses (0.3-0.6 nA, 600 ms) revealed that augmentation decays with time. The integral of EPSPs evoked approximately 80 ms after the onset of the current pulse was 3.7 (+/- 1.5, n = 16) times larger than at Em. The integral of EPSPs evoked at 480 ms. however, were only twofold (+/- 0.7, n = 16) larger. Hence EPSPs evoked after a delay of 80 ms were 1.7-fold (+/- 0.4, n = 24) larger than EPSPs evoked after 480 ms. EPSCs were independent of the delay of stimulation at all potentials. 5. Intracellular application of the lidocaine derivative N-(2,6-dimethyl-phenylcarbamoylmethyl) triethylammonium bromide (QX 314) at 100 mM from pipettes rapidly abolished fast action potentials and inward rectification. During comparable depolarizations the increase in EPSP integrals was much smaller in QX 314-treated neurons than in controls. On average, the integral of EPSPs evoked at 70-90 ms was 1.7 times (+/- 1.0) larger than at Em, and the integral of EPSPs evoked with larger delays was close to the value obtained at resting Em (0.9 +/- 0.3, n = 8). The ratio of EPSP integrals early versus late (1.8 +/- 0.5) is comparable to controls, suggesting that QX 314-sensitive currents are unlikely to be involved in the time-dependent enhancement. 6. Mimicking EPSPs by brief depolarizations atop long depolarizations revealed a time- and voltage-dependent enhancement comparable to that of EPSPs.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用快速单电极电流 - 电压钳技术在体外研究大鼠新皮质神经元兴奋性突触后电位(EPSP)的特性。通常,通过选择低强度电刺激可获得明显纯净的EPSP。2. 当神经元去极化时,EPSP的幅度和时间积分增加。在动作电位产生阈值时,EPSP的幅度增加约30%[从5.0±2.1mV增加到6.3±1.0(标准差)mV,n = 12]。EPSP的积分最大比静息膜电位(Em)时大约大四倍(3.7±1.5,n = 16)。进一步研究了EPSP增强所涉及的机制。3. 随着指令电位从 - 100mV向 - 60mV移动,兴奋性突触后电流(EPSC)的幅度和时间积分呈线性下降。EPSC积分随去极化而降低表明,EPSP的增强可能是由电压依赖性内向电流的募集引起的。4. 在小的去极化电流脉冲(0.3 - 0.6nA,600ms)开始后的不同延迟时间诱发EPSP,结果显示增强随时间衰减。在电流脉冲开始后约80ms诱发的EPSP积分比Em时大3.7(±1.5,n = 16)倍。然而,在480ms时诱发的EPSP积分仅大二倍(±0.7,n = 16)。因此,在80ms延迟后诱发的EPSP比在480ms后诱发的EPSP大1.7倍(±0.4,n = 24)。在所有电位下,EPSC均与刺激延迟无关。5. 从微电极内向施加100mM的利多卡因衍生物N -(2,6 - 二甲基 - 苯基氨基甲酰甲基)三乙铵溴化物(QX 314)可迅速消除快速动作电位和内向整流。在可比的去极化过程中,QX 314处理的神经元中EPSP积分的增加比对照组小得多。平均而言,在70 - 90ms诱发的EPSP积分比Em时大1.7倍(±1.0),而在更大延迟时诱发的EPSP积分接近静息Em时的值(0.9±0.3,n = 8)。早期与晚期EPSP积分的比值(1.8±0.5)与对照组相当,这表明QX 314敏感电流不太可能参与时间依赖性增强。6. 通过在长时去极化之上进行短暂去极化来模拟EPSP,发现其时间和电压依赖性增强与EPSP相当。(摘要截断于400字)

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