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Possible relationship between the stress‐induced synaptic response and metaplasticity in the hippocampal CA1 field of freely moving rats
Author(s) -
Hirata Riki,
Matsumoto Machiko,
Judo Chika,
Yamaguchi Taku,
Izumi Takeshi,
Yoshioka Mitsuhiro,
Togashi Hiroko
Publication year - 2009
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.20631
Subject(s) - long term potentiation , metaplasticity , neuroscience , synaptic plasticity , hippocampal formation , hippocampus , population spike , ltp induction , synaptic fatigue , synapse , stimulation , neurotransmission , psychology , chemistry , excitatory postsynaptic potential , dentate gyrus , inhibitory postsynaptic potential , receptor , biochemistry
Hippocampal long‐term potentiation (LTP) is suppressed not only by stress paradigms but also by low frequency stimulation (LFS) prior to LTP‐inducing high frequency stimulation (HFS; tetanus), termed metaplasticity. These synaptic responses are dependent on N ‐methyl‐ D ‐aspartate receptors, leading to speculations about the possible relationship between metaplasticity and stress‐induced LTP impairment. However, the functional significance of metaplasticity has been unclear. The present study elucidated the electrophysiological and neurochemical profiles of metaplasticity in the hippocampal CA1 field, with a focus on the synaptic response induced by the emotional stress, contextual fear conditioning (CFC). The population spike amplitude in the CA1 field was decreased during exposure to CFC, and LTP induction was suppressed after CFC in conscious rats. The synaptic response induced by CFC was mimicked by LFS, i.e., LFS impaired the synaptic transmission and subsequent LTP. Plasma corticosterone levels were increased by both CFC and LFS. Extracellular levels of γ‐aminobutyric acid (GABA), but not glutamate, in the hippocampus increased during exposure to CFC or LFS. Furthermore, electrical stimulation of the medial prefrontal cortex (mPFC), which caused decreases in freezing behavior during exposure to CFC, counteracted the LTP impairment induced by LFS. These findings suggest that metaplasticity in the rat hippocampal CA1 field is related to the neural basis of stress experience‐dependent fear memory, and that hippocampal synaptic response associated stress‐related processes is under mPFC regulation. Synapse 63:549‐556, 2009. © 2009 Wiley‐Liss, Inc.