Reduced expression of complexins I and II in rats bred for learned helplessness

被引:11
作者
Zink, Mathias
Vollmayr, Barbara
Gebicke-Haerter, Peter J.
Henn, Fritz A.
Thome, Johannes
机构
[1] Cent Inst Mental Hlth, Dept Psychiat & Psychotherapy, D-68072 Mannheim, Germany
[2] Brookhaven Natl Lab, New York, NY 11973 USA
[3] Univ Coll Swansea, Sch Med, Dept Psychiat, Swansea, W Glam, Wales
关键词
animal model; complexin; depression; synapse; learned helplessness;
D O I
10.1016/j.brainres.2007.01.066
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Disturbed synaptic transmission contributes to the pathophysiology of mood disorders. Post mortem studies reported reduced expression of the synaptic vesicle protein (SVP) complexins I and II in depression. Antidepressants were found to induce the expression of these genes. Since animals with congenital susceptibility to learned helplessness provide a valid animal model of depression, we investigated the expression of different SVPs in this system by semiquantitative in situ hybridization. Rats bred for congenital learned helpless behavior (cLH, N=6) failed to interrupt foot shock currents by lever pressing (mean 12.3 failures out of 15 trials). These animals showed significantly lower expression of complexins I and II mRNA in hippocampal, limbic and cortical brain areas compared to not helpless animals (cNLH, N=6) with a mean failure rate of 0.83 out of 15 trials. Expression levels of complexins I and II significantly correlated with the failure rate in the test paradigm. In contrast, the expressions of synaptotagmin I and synaptophysin were found unchanged. This investigation provides a further validation of the LH model of depression. The experimental data fit well into current pathogenetic concepts of mood disorders and support the hypothesis, that complexins are pivotal players in the pathophysiology of depression and tentative targets of antidepressants. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:202 / 208
页数:7
相关论文
共 37 条
[1]   Proteome analysis of human substantia nigra in Parkinson's disease [J].
Basso, M ;
Giraudo, S ;
Corpillo, D ;
Bergamasco, B ;
Lopiano, L ;
Fasano, M .
PROTEOMICS, 2004, 4 (12) :3943-3952
[2]   Finding the intracellular signaling pathways affected by mood disorder treatments [J].
Coyle, JT ;
Duman, RS .
NEURON, 2003, 38 (02) :157-160
[3]   Early changes in Huntington's disease patient brains involve alterations in cytoskeletal and synaptic elements [J].
DiProspero, NA ;
Chen, EY ;
Charles, V ;
Plomann, M ;
Kordower, JH ;
Tagle, DA .
JOURNAL OF NEUROCYTOLOGY, 2004, 33 (05) :517-533
[4]   Hippocampal synaptic pathology in schizophrenia, bipolar disorder and major depression: a study of complexin mRNAs [J].
Eastwood, SL ;
Harrison, PJ .
MOLECULAR PSYCHIATRY, 2000, 5 (04) :425-432
[5]   Synaptic pathology in the anterior cingulate cortex in schizophrenia and mood disorders. A review and a Western blot study of synaptophysin, GAP-43 and the complexins [J].
Eastwood, SL ;
Harrison, PJ .
BRAIN RESEARCH BULLETIN, 2001, 55 (05) :569-578
[6]   Differential messenger RNA expression of complexins in mouse brain [J].
Freeman, W ;
Morton, AJ .
BRAIN RESEARCH BULLETIN, 2004, 63 (01) :33-44
[7]  
Garcia R, 2002, REV NEUROSCIENCE, V13, P195
[8]   A clamping mechanism involved in SNARE-dependent exocytosis [J].
Giraudo, Claudio G. ;
Eng, William S. ;
Melia, Thomas J. ;
Rothman, James E. .
SCIENCE, 2006, 313 (5787) :676-680
[9]   Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits [J].
Glynn, D ;
Drew, CJ ;
Reim, K ;
Brose, N ;
Morton, AJ .
HUMAN MOLECULAR GENETICS, 2005, 14 (16) :2369-2385
[10]   Complexin II is essential for normal neurological function in mice [J].
Glynn, D ;
Bortnick, RA ;
Morton, AJ .
HUMAN MOLECULAR GENETICS, 2003, 12 (19) :2431-2448