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从豚鼠海马切片的CA1锥体细胞记录到的小兴奋性突触后电位(EPSP)的幅度波动。

Amplitude fluctuations in small EPSPs recorded from CA1 pyramidal cells in the guinea pig hippocampal slice.

作者信息

Sayer R J, Redman S J, Andersen P

机构信息

Experimental Neurology Unit, John Curtin School of Medical Research, Australian National University, Canberra.

出版信息

J Neurosci. 1989 Mar;9(3):840-50. doi: 10.1523/JNEUROSCI.09-03-00840.1989.

Abstract

EPSPs have been evoked in CA1 pyramidal cells by (1) activation of single CA3 neurons (unitary EPSPs), and (2) low-intensity stimuli to the CA1 stratum radiatum. Five unitary EPSPs were obtained; their mean peak amplitudes ranged from 85 to 275 microV and 3 of the 5 showed fluctuations in amplitude that were too great to be attributed to baseline noise. After subtraction of the variance due to the noise, these EPSPs had coefficients of variation much higher than those reported for variability in the quantal EPSP in other preparations. These results suggest that intermittent transmitter release is a major cause of EPSP amplitude fluctuation at this synapse. A noise deconvolution technique based on a nonrestrictive model of transmitter release was applied to the EPSPs obtained in this study. For 2 of the EPSPs evoked by stratum radiatum stimulation, the amplitudes fluctuated between discrete values that were sufficiently separated with respect to the noise to be resolved by the deconvolution procedure. Quantal increments of 224 and 193 microV were determined for the 2 EPSPs.

摘要

通过以下方式在CA1锥体细胞中诱发了兴奋性突触后电位(EPSP):(1)激活单个CA3神经元(单一EPSP),以及(2)对CA1辐射层进行低强度刺激。获得了5个单一EPSP;它们的平均峰值幅度在85至275微伏之间,5个中有3个的幅度波动太大,不能归因于基线噪声。在减去噪声引起的方差后,这些EPSP的变异系数远高于其他制剂中量子EPSP变异性所报道的系数。这些结果表明,间歇性递质释放是该突触处EPSP幅度波动的主要原因。基于递质释放的非限制性模型的噪声反卷积技术应用于本研究中获得的EPSP。对于由辐射层刺激诱发的2个EPSP,其幅度在离散值之间波动,这些离散值相对于噪声充分分离,可通过反卷积程序分辨。确定这2个EPSP的量子增量分别为224和193微伏。

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