Proteomic analysis of rat hippocampus after repeated psychosocial stress

被引:59
作者
Carboni, L
Piubielli, C
Pozzato, C
Astner, H
Arban, R
Righietti, PG
Hamdan, M
Domenici, E
机构
[1] GlaxoSmithKline, Dept Behav Neurosci, Psychiat Ctr Excellence Drug Discovery, I-37135 Verona, Italy
[2] GlaxoSmithKline, Dept Mol Psychiat, Psychiat Ctr Excellence Drug Discovery, I-37135 Verona, Italy
[3] GlaxoSmithKline, Dept Neuropsychopharmacol, Psychiat Ctr Excellence Drug Discovery, I-37135 Verona, Italy
[4] GlaxoSmithKline, Discovery Res, Dept Computat Analyt & Struct Sci, I-37135 Verona, Italy
[5] Univ Verona, Dept Agr & Ind Biotechnol, I-37134 Verona, Italy
关键词
social defeat; 2-D electrophoresis; mass spectrometry; behavioral model; rat brain;
D O I
10.1016/j.neuroscience.2005.10.045
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (c) 2005 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1237 / 1246
页数:10
相关论文
共 66 条
[11]   Application of proteomics technologies in the investigation of the brain [J].
Fountoulakis, M .
MASS SPECTROMETRY REVIEWS, 2004, 23 (04) :231-258
[12]   Stress, glucocorticoids and structural plasticity of the hippocampus [J].
Fuchs, E ;
Flügge, G .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1998, 23 (02) :295-300
[13]   Social stress in tree shrews:: Effects on physiology, brain function, and behavior of subordinate individuals [J].
Fuchs, E ;
Flügge, G .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 73 (01) :247-258
[14]   CRMP-2 binds to tubulin heterodimers to promote microtubule assembly [J].
Fukata, Y ;
Itoh, TJ ;
Kimura, T ;
Ménager, C ;
Nishimura, T ;
Shiromizu, T ;
Watanabe, H ;
Inagaki, N ;
Iwamatsu, A ;
Hotani, H ;
Kaibuchi, K .
NATURE CELL BIOLOGY, 2002, 4 (08) :583-591
[15]   Psychophysiological stress induces heat shock cognate protein 70 messenger RNA in the hippocampus of rats [J].
Fukudo, S ;
Abe, K ;
Itoyama, Y ;
Mochizuki, S ;
Sawai, T ;
Hongo, M .
NEUROSCIENCE, 1999, 91 (04) :1205-1208
[16]   PSYCHOPHYSIOLOGICAL STRESS INDUCES HEAT-SHOCK COGNATE PROTEIN (HSC)70 MESSENGER-RNA IN THE CEREBRAL-CORTEX AND STOMACH OF RATS [J].
FUKUDO, S ;
ABE, K ;
HONGO, M ;
UTSUMI, A ;
ITOYAMA, Y .
BRAIN RESEARCH, 1995, 675 (1-2) :98-102
[17]   Glucocorticoid upregulation of glutamate dehydrogenase gene expression in vitro in astrocytes [J].
HardinPouzet, H ;
Giraudon, P ;
Belin, MF ;
DidierBazes, M .
MOLECULAR BRAIN RESEARCH, 1996, 37 (1-2) :324-328
[18]  
Hayase Tamaki, 2003, Leg Med (Tokyo), V5 Suppl 1, pS87, DOI 10.1016/S1344-6223(02)00093-7
[19]   Peptidyl prolyl cis-trans isomerase activity of cyclophilin A in functional homo-oligomeric receptor expression [J].
Helekar, SA ;
Patrick, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5432-5437
[20]  
Herbert B, 2001, ELECTROPHORESIS, V22, P2046, DOI 10.1002/1522-2683(200106)22:10<2046::AID-ELPS2046>3.0.CO