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大鼠海马切片齿状回抑制性突触传递的量子分析:一项膜片钳研究。

Quantal analysis of inhibitory synaptic transmission in the dentate gyrus of rat hippocampal slices: a patch-clamp study.

作者信息

Edwards F A, Konnerth A, Sakmann B

机构信息

Max-Planck-Institut für medizinische Forschung, Abteilung Zellphysiologie, Heidelberg, FRG.

出版信息

J Physiol. 1990 Nov;430:213-49. doi: 10.1113/jphysiol.1990.sp018289.

DOI:10.1113/jphysiol.1990.sp018289
PMID:1707966
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1181735/
Abstract
  1. Synaptically connected neurones were identified in the granule cell layer of slices of 17- to 21-day-old rat hippocampus. Whole-cell current recording using the patch-clamp technique revealed synaptic currents ranging from less than 10 to 200 pA in symmetrical Cl- conditions, at a holding potential of -50 mV. These currents were blocked by 2 microM-bicuculline, indicating that they result from the activation of postsynaptic gamma-aminobutyric acid receptor (GABAA-receptor) channels. 2. Addition of tetrodotoxin (TTX, 1 microM) resulted in the loss of most currents of more than 40 pA in amplitude. Currents which disappeared after TTX treatment were assumed to be the result of spontaneous presynaptic action potentials. The currents seen in the absence of TTX are referred to as spontaneously occurring inhibitory postsynaptic currents (IPSCs); those remaining in the presence of TTX were defined as miniature IPSCs. 3. Similar currents were observed when recording in the whole-cell configuration while extracellular stimulation was applied to a nearby neurone. These currents were also completely blocked by 2 microM-bicuculline and by 0.5 microM-TTX. They were thus defined as stimulus-evoked IPSCs. 4. The half rise time of both miniature and stimulus-evoked IPSCs was fast (less than 1 ms). The time course of decay of both miniature IPSCs and stimulus-evoked IPSCs could be well fitted with the sum of two exponentials. At a membrane potential of -50 mV, the mean decay time constants of the two components were 2.0 +/- 0.38 and 54.4 +/- 18 ms (mean +/- S.D.) for miniature IPSCs (six cells) and 2.2 +/- 1.3 and 66 +/- 20 ms (three cells) for stimulus-evoked IPSCs. 5. Stimulus-evoked IPSCs varied in amplitude from less than ten to hundreds of picoamperes. In eight of eleven cells histograms of IPSC amplitudes showed several clear peaks which, when fitted with the sum of Gaussian curves, were found to be equidistant. This is consistent with the view that stimulus-evoked IPSC amplitudes vary in a quantal fashion. The quantal size varied between 7 and 20 pA, at a membrane potential of -50 mV. 6. Decreasing the Ca2+ and increasing the Mg2+ concentration in the extracellular solution decreased the number of peaks in the IPSC amplitude histogram but did not affect the size of the quantal event.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在17至21日龄大鼠海马切片的颗粒细胞层中鉴定出了突触连接的神经元。在对称氯离子条件下,于-50 mV的钳制电位下,采用膜片钳技术进行全细胞电流记录,显示突触电流范围为小于10至200 pA。这些电流被2 μM荷包牡丹碱阻断,表明它们是由突触后γ-氨基丁酸受体(GABAA受体)通道的激活所导致。2. 添加河豚毒素(TTX,1 μM)导致幅度大于40 pA的大多数电流消失。TTX处理后消失的电流被认为是自发突触前动作电位的结果。在无TTX时观察到的电流被称为自发产生的抑制性突触后电流(IPSCs);在存在TTX时仍存在的电流被定义为微小IPSCs。3. 在全细胞模式下记录时,当对附近神经元施加细胞外刺激时,观察到了类似的电流。这些电流也被2 μM荷包牡丹碱和0.5 μM TTX完全阻断。因此,它们被定义为刺激诱发的IPSCs。4. 微小IPSCs和刺激诱发的IPSCs的半上升时间都很快(小于1 ms)。微小IPSCs和刺激诱发的IPSCs的衰减时间进程都可以很好地用两个指数之和来拟合。在-50 mV的膜电位下,微小IPSCs(六个细胞)的两个成分的平均衰减时间常数分别为2.0±0.38和54.4±18 ms(平均值±标准差),刺激诱发的IPSCs(三个细胞)的分别为2.2±1.3和66±20 ms。5. 刺激诱发的IPSCs的幅度从小于十皮安到数百皮安不等。在11个细胞中的8个细胞中,IPSC幅度的直方图显示有几个明显的峰值,当用高斯曲线之和拟合时,发现它们是等距的。这与刺激诱发的IPSC幅度以量子方式变化的观点一致。在-50 mV的膜电位下,量子大小在7至20 pA之间变化。6. 降低细胞外溶液中的Ca2+浓度并增加Mg2+浓度会减少IPSC幅度直方图中的峰值数量,但不影响量子事件的大小。(摘要截短至400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/addc/1181735/18b2ca5cf878/jphysiol00456-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/addc/1181735/18b2ca5cf878/jphysiol00456-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/addc/1181735/18b2ca5cf878/jphysiol00456-0258-a.jpg

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