Effect of subacute and chronic immobilisation stress on the outcome of permanent focal cerebral ischaemia in rats

被引:60
作者
Madrigal, JLM [1 ]
Caso, JR [1 ]
de Cristóbal, J [1 ]
Cárdenas, A [1 ]
Leza, JC [1 ]
Lizasoain, I [1 ]
Lorenzo, P [1 ]
Moro, MA [1 ]
机构
[1] Univ Complutense Madrid, Fac Med, Dept Farmacol, E-28040 Madrid, Spain
关键词
mood disorder; glutamate transporter; brain ATP; excitotoxicity;
D O I
10.1016/S0006-8993(03)02892-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The aim of this study was to determine the effect of mood disorders, including psychological distress and depression, on stroke outcome. Male Fischer rats were exposed to immobilisation stress, an animal paradigm of psychological stress, major depression and post-traumatic stress disorder. Either a subacute (1 h for 7 days) or a chronic (6 h for 21 days) exposure to stress was applied 24 h before permanent middle cerebral artery occlusion (MCAO). Stroke outcome was assessed by measurement of infarct size and behavioural characterisation. Serum glutamate and brain ATP levels as well as brain glutamate transporter function and expression were studied in the search for the molecular mechanisms involved. Subacute stress exposure increased infarct size and decreased behavioural scores after stroke. On the contrary, chronic stress exposure decreased infarct size. Peak serum glutamate levels correlated with infarct size after MCAO. Expression of glutamate transporters was decreased by subacute stress, whereas the expression of EAAT1, a glial glutamate carrier, was increased after the chronic stress protocol. Our results indicate that distinct patterns of stress determine different stroke outcomes, and that expressional changes of brain glutamate transporters, able to affect glutamate release after stroke, are involved. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:137 / 145
页数:9
相关论文
共 47 条
[1]   INTRAISCHEMIC HYPOTHERMIA DECREASES THE RELEASE OF GLUTAMATE IN THE CORES OF PERMANENT FOCAL CEREBRAL INFARCTS [J].
BAKER, CJ ;
FIORE, AJ ;
FRAZZINI, VI ;
CHOUDHRI, TF ;
ZUBAY, GP ;
SOLOMON, RA .
NEUROSURGERY, 1995, 36 (05) :994-1001
[2]  
BREMNER JD, 1991, PTSD RES Q, V2, P1
[3]   Progression of ischaemic stroke and excitotoxic aminoacids [J].
Castillo, J ;
Davalos, A ;
Noya, M .
LANCET, 1997, 349 (9045) :79-83
[4]   Neuroexcitatory amino acids and their relation to infarct size and neurological deficit in ischemic stroke [J].
Castillo, J ;
Davalos, A ;
Naveiro, J ;
Noya, M .
STROKE, 1996, 27 (06) :1060-1065
[5]  
CHOI DW, 1990, ANNU REV NEUROSCI, V13, P171, DOI 10.1146/annurev.neuro.13.1.171
[6]   DEPRESSIVE SYMPTOMS AND OTHER PSYCHOSOCIAL FACTORS AS PREDICTORS OF STROKE IN THE ELDERLY [J].
COLANTONIO, A ;
KASL, SV ;
OSTFELD, AM .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1992, 136 (07) :884-894
[7]   Repeated restraint stress facilitates fear conditioning independently of causing hippocampal CA3 dendritic atrophy [J].
Conrad, CD ;
Magariños, AM ;
LeDoux, JE ;
McEwen, BS .
BEHAVIORAL NEUROSCIENCE, 1999, 113 (05) :902-913
[8]  
DAVALOS A, 2000, J STROKE CEREBROVASC, V9, pS2
[9]   Aspirin inhibits stress-induced increase in plasma glutamate, brain oxidative damage and ATP fall in rats [J].
De Cristóbal, J ;
Madrigal, JLM ;
Lizasoain, I ;
Lorenzo, P ;
Leza, JC ;
Moro, MA .
NEUROREPORT, 2002, 13 (02) :217-221
[10]   Inhibition of glutamate release via recovery of ATP levels accounts for a neuroprotective effect of aspirin in rat cortical neurons exposed to oxygen-glucose deprivation [J].
De Cristóbal, J ;
Cárdenas, A ;
Lizasoain, I ;
Leza, JC ;
Fernández-Tomé, P ;
Lorenzo, P ;
Moro, MA .
STROKE, 2002, 33 (01) :261-267