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Neurobiol Dis. 2013 Apr;52:160-7. doi: 10.1016/j.nbd.2012.12.003. Epub 2012 Dec 20.

GluA1 and its PDZ-interaction: a role in experience-dependent behavioral plasticity in the forced swim test.

Author information

1
Laboratory of Neural Circuits and Plasticity, University of Southern California, 3641 Watt Way, Los Angeles, CA-90089, USA. ffreuden@gmail.com

Abstract

Glutamate receptor dependent synaptic plasticity plays an important role in the pathophysiology of depression. Hippocampal samples from clinically depressed patients display reduced mRNA levels for GluA1, a major subunit of AMPA receptors. Moreover, activation and synaptic incorporation of GluA1-containing AMPA receptors are required for the antidepressant-like effects of NMDA receptor antagonists. These findings argue that GluA1-dependent synaptic plasticity might be critically involved in the expression of depression. Using an animal model of depression, we demonstrate that global or hippocampus-selective deletion of GluA1 impairs expression of experience-dependent behavioral despair. This impairment is mediated by the interaction of GluA1 with PDZ-binding domain proteins, as deletion of the C-terminal leucine alone is sufficient to replicate the behavioral phenotype. Our results provide evidence for a significant role of hippocampal GluA1-containing AMPA receptors and their PDZ-interaction in experience-dependent expression of behavioral despair and link mechanisms of hippocampal synaptic plasticity with behavioral expression of depression.

PMID:
23262314
DOI:
10.1016/j.nbd.2012.12.003
[Indexed for MEDLINE]

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