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豚鼠海马锥体细胞中的前馈抑制电位和兴奋性相互作用。

Feed-forward inhibitory potentials and excitatory interactions in guinea-pig hippocampal pyramidal cells.

作者信息

Turner D A

机构信息

University of Minnesota, Minneapolis.

出版信息

J Physiol. 1990 Mar;422:333-50. doi: 10.1113/jphysiol.1990.sp017987.

Abstract
  1. The patterns of inhibition in the CA1 region of the rat hippocampus were evaluated by focal proximal and distal stratum radiatum stimulation, during intracellular recording. The characteristics of isolated inhibitory responses and the interactions of excitatory and inhibitory potentials were analysed. 2. The amplitude of minimal inhibitory postsynaptic potentials (IPSPs) evoked by both proximal and distal stimulation averaged -0.51 +/- 0.24 mV (mean +/- S.D.; n = 32). These responses demonstrated little variability from trial to trial and showed no net trends in amplitude at a stimulation rate of 1 Hz. 3. Minimal IPSPs demonstrated a short latency to onset (2.90 +/- 1.58 ms for proximal and 3.64 +/- 1.39 ms for distal) at stimulation levels which were insufficient to evoke an extracellular field potential. Thus, minimal IPSPs were recruited through feed-forward circuitry, based on the rapid onset and the lack of activation of recurrent collaterals. 4. The minimal IPSPs showed a similar 10-90% rise time for proximal and distal responses. However, the half-width and decay time constant (from the peak) were more prolonged for the distal stimulation, indicating that a late IPSP component was evoked primarily by the distal stimulation. This late component was not observed in isolation at low stimulation intensities. 5. The conductance transient underlying the IPSPs was calculated using a neurone cable model. The proximal IPSP responses were simulated by an alpha input function (at the soma) with a peak conductance in the range of 2.5-45 nS (alpha = 1.75; reversal potential -1.0 to -10 mV). The distal IPSP shape was only partially reproduced by a longer single transient (alpha = 1.25), suggesting the presence of a second, slower component. However, insufficient data on this slower component precluded a more exact simulation of the distal IPSP response. 6. Analysis of interactions between minimal excitatory postsynaptic potentials (EPSPs) and IPSPs showed that often the rising as well as the falling phase of the EPSP could be affected by the IPSP. At small stimulation levels, minimal EPSPs and IPSPs were closely overlapping, but the IPSPs were of significantly longer duration than EPSP responses. 7. The composite EPSP waveform shape became progressively truncated with increasing afferent stimulation. Feed-forward inhibition limited the time course of excitation to a narrow window, approximately 3-5 ms wide. Feed-forward postsynaptic inhibition significantly limited both the duration and the overall efficacy of small EPSPs in CA1 pyramidal neurones.
摘要
  1. 在细胞内记录过程中,通过对大鼠海马体CA1区近端和远端辐射层进行局部刺激,评估抑制模式。分析了孤立抑制反应的特征以及兴奋性和抑制性电位的相互作用。2. 近端和远端刺激诱发的最小抑制性突触后电位(IPSPs)的幅度平均为-0.51±0.24 mV(平均值±标准差;n = 32)。这些反应在每次试验中变化很小,在1 Hz的刺激频率下,幅度没有净趋势。3. 在不足以诱发细胞外场电位的刺激水平下,最小IPSPs的起始潜伏期较短(近端为2.90±1.58 ms,远端为3.64±1.39 ms)。因此,基于快速起始和缺乏回返侧支的激活,最小IPSPs是通过前馈回路募集的。4. 近端和远端反应的最小IPSPs的10-90%上升时间相似。然而,远端刺激的半宽度和衰减时间常数(从峰值开始)更长,表明远端刺激主要诱发了一个晚期IPSP成分。在低刺激强度下未单独观察到这个晚期成分。5. 使用神经元电缆模型计算了IPSPs背后的电导瞬变。近端IPSP反应由α输入函数(在胞体处)模拟,峰值电导在2.5-45 nS范围内(α = 1.75;反转电位-1.0至-10 mV)。远端IPSP形状仅由一个更长的单个瞬变部分再现(α = 1.25),表明存在第二个较慢的成分。然而,关于这个较慢成分的数据不足,无法更精确地模拟远端IPSP反应。6. 对最小兴奋性突触后电位(EPSPs)和IPSPs之间相互作用的分析表明,EPSP的上升和下降阶段通常都可能受到IPSP的影响。在小刺激水平下,最小EPSPs和IPSPs紧密重叠,但IPSPs的持续时间明显长于EPSP反应。7. 随着传入刺激增加,复合EPSP波形形状逐渐被截断。前馈抑制将兴奋的时间进程限制在一个狭窄的窗口内,大约3-5 ms宽。前馈突触后抑制显著限制了CA1锥体神经元中小EPSPs的持续时间和总体效能。

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