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Proteomic analysis of rat hippocampus after repeated psychosocial stress

Authors :
Pier Giorgio Righetti
Mahmoud Hamdan
Chiara Pozzato
Lucia Carboni
Chiara Piubelli
Hubert Astner
Roberto Arban
Enrico Domenici
Carboni L.
Piubelli C.
Pozzato C.
Astner H.
Arban R.
Righetti P.G.
Hamdan M.
Domenici E.
Source :
Neuroscience. 137:1237-1246
Publication Year :
2006
Publisher :
Elsevier BV, 2006.

Abstract

Since stress plays a role in the onset and physiopathology of psychiatric diseases, animal models of chronic stress may offer insights into pathways operating in mood disorders. The aim of this study was to identify the molecular changes induced in rat hippocampus by repeated exposure to psychosocial stress with a proteomic technique. In the social defeat model, the experimental animal was defeated by a dominant male eight times. Additional groups of rats were submitted to a single defeat or placed in an empty cage (controls). The open field test was carried out on parallel animal groups. The day after the last exposure, levels of hippocampal proteins were compared between groups after separation by 2-D gel electrophoresis and image analysis. Spots showing significantly altered levels were submitted to peptide fingerprinting mass spectrometry for protein identification. The intensity of 69 spots was significantly modified by repeated stress and 21 proteins were unambiguously identified, belonging to different cellular functions, including protein folding, signal transduction, synaptic plasticity, cytoskeleton regulation and energy metabolism. This work identified molecular changes in protein levels caused by exposure to repeated psychosocial stress. The pattern of changes induced by repeated stress was quantitatively and qualitatively different from that observed after a single exposure. Several changed proteins have already been associated with stress-related responses; some of them are here described for the first time in relation to stress.

Details

ISSN :
03064522
Volume :
137
Database :
OpenAIRE
Journal :
Neuroscience
Accession number :
edsair.doi.dedup.....f0590d32f1c89d7495ae7b938a1915d6
Full Text :
https://doi.org/10.1016/j.neuroscience.2005.10.045