4.4 Article

Mechanisms underlying rule learning-induced enhancement of excitatory and inhibitory synaptic transmission

期刊

JOURNAL OF NEUROPHYSIOLOGY
卷 107, 期 4, 页码 1222-1229

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.00356.2011

关键词

olfactory learning; piriform cortex; miniature synaptic currents

资金

  1. Israel Science Foundation

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Saar D, Reuveni I, Barkai E. Mechanisms underlying rule learning-induced enhancement of excitatory and inhibitory synaptic transmission. J Neurophysiol 107: 1222-1229, 2012. First published November 30, 2011; doi:10.1152/jn.00356.2011.-Training rats to perform rapidly and efficiently in an olfactory discrimination task results in robust enhancement of excitatory and inhibitory synaptic connectivity in the rat piriform cortex, which is maintained for days after training. To explore the mechanisms by which such synaptic enhancement occurs, we recorded spontaneous miniature excitatory and inhibitory synaptic events in identified piriform cortex neurons from odor-trained, pseudo-trained, and naive rats. We show that olfactory discrimination learning induces profound enhancement in the averaged amplitude of AMPA receptor-mediated miniature synaptic events in piriform cortex pyramidal neurons. Such physiological modifications are apparent at least 4 days after learning completion and outlast learning-induced modifications in the number of spines on these neurons. Also, the averaged amplitude of GABA(A) receptor-mediated miniature inhibitory synaptic events was significantly enhanced following odor discrimination training. For both excitatory and inhibitory transmission, an increase in miniature postsynaptic current amplitude was evident in most of the recorded neurons; however, some neurons showed an exceptionally great increase in the amplitude of miniature events. For both excitatory and inhibitory transmission, the frequency of spontaneous synaptic events was not modified after learning. These results suggest that olfactory discrimination learning-induced enhancement of synaptic transmission in cortical neurons is mediated by postsynaptic modulation of AMPA receptor-dependent currents and balanced by long-lasting modulation of postsynaptic GABA(A) receptor-mediated currents.

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