Behavioral deficits and recovery following transient focal cerebral ischemia in rats: glutamatergic and GABAergic receptor densities

被引:27
作者
Jolkkonen, J
Gallagher, NP
Zilles, K
Sivenius, J
机构
[1] Univ Kuopio, Dept Neurol & Neurosci, FIN-70211 Kuopio, Finland
[2] Univ Dusseldorf, C&O Vogt Inst Brain Res, D-4000 Dusseldorf, Germany
[3] Res Ctr, Inst Med, Julich, Germany
[4] Kuopio Univ Hosp, Dept Neurol, Brain Res & Rehabil Ctr Neuron, SF-70210 Kuopio, Finland
关键词
enriched environment; functional recovery; GABA(A) receptor; ionotropic glutamate receptors; middle cerebral artery occlusion; sensorimotor deficit; spatial learning deficit;
D O I
10.1016/S0166-4328(02)00241-3
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The neurobiologic mechanisms underlying the recovery process following stroke are poorly understood. The present study investigated glutamatergic and gamma-amino butyric acid (GABA)-ergic receptor densities following experimental stroke in rats exposed to different environmental housing or pharmacologic interventions. About 2 days after transient (120 min) middle cerebral artery (MCA) occlusion, the rats were singly housed in standard cages or were moved to an enriched environment and treated for 10 days with either 0.9% NaCl or with the alpha(2)-adrenoceptor antagonist, atipamezole (1.0 mg/kg, s.c.). The limb-placing, foot-slip, and watermaze tests were used to assess behavioral deficits and recovery following ischemia. The rats were decapitated on day 25 after the operation and their brains were processed for [H-3]MK-801, [H-3]D,L,-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), [H-3]kainate, and [H-3]muscimol autoradiography. Receptor binding site densities were different between sham-operated rats and ischemic rats only in the lesion core and lateral ventroposterior thalamic nucleus. Ischemic rats housed in an enriched environment and treated with atipamezole had better performance in the limb-placing test. The deficit in the water-maze test was most pronounced in ischemic rats housed in standard cages. There were a number of correlations between the behavioral data and receptor binding densities in ischemic rats. For example, recovery in the limb-placing test correlated with [H-3]AMPA receptor binding sites in the contralateral frontal cortex (r = 0.616, P < 0.05), hindlimb cortex (r = 0.649, P < 0.05), and parietal cortex (r = 0.674, P < 0.05) in ischemic rats housed in an enriched environment. There were similar correlations between limb-placing recovery and [H-3]kainate binding sites in the contralateral cortices in ischemic rats housed in standard cages. In addition, there were particularly strong clustered correlations between swimming speed in the water-maze test and [H-3]AMPA receptor binding sites in the hippocampal subregions in the ischemic rats housed in an enriched environment. The present results suggest that transient focal cerebral ischemia does not induce significant long-term changes in glutamatergic and GABAergic receptors in areas remote from the infarct area. The correlational data, however, suggest an important role for the contralateral cortex in the behavioral outcome and maintenance of the recovered state of ischemic rats, depending on housing conditions. In addition, attenuation of spatial learning deficits observed in ischemic rats housed in an enriched environment might be due to an increase in the swimming speed through hippocampal AMPA receptor-mediated mechanisms. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:187 / 200
页数:14
相关论文
共 60 条
[1]   Hippocampal dependent learning ability correlates with N-methyl-D-aspartate (NMDA) receptor levels in CA3 neurons of young and aged rats [J].
Adams, MM ;
Smith, TD ;
Moga, D ;
Gallagher, M ;
Wang, Y ;
Wolfe, BB ;
Rapp, PR ;
Morrison, JH .
JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 432 (02) :230-243
[2]  
Altman DG, 1990, PRACTICAL STAT MED R
[3]   Differentially altered cerebral metabolism in ischemic rats by α2-adrenoceptor blockade and its relation to improved limb-placing reactions [J].
Barbelivien, A ;
Jolkkonen, J ;
Rutkauskaite, E ;
Sirviö, J ;
Sivenius, J .
NEUROPHARMACOLOGY, 2002, 42 (01) :117-126
[4]  
Bidmon HJ, 1998, NEUROSCIENCE, V82, P397
[5]  
BLADIN F, 1998, CEREBROVASC DIS, P1119
[6]  
Butovas S, 2001, RESTOR NEUROL NEUROS, V18, P143
[7]   FEEDFORWARD INHIBITION IN THE HIPPOCAMPAL-FORMATION [J].
BUZSAKI, G .
PROGRESS IN NEUROBIOLOGY, 1984, 22 (02) :131-153
[8]   The problem of assessing effective neuroprotection in experimental cerebral ischemia [J].
Corbett, D ;
Nurse, S .
PROGRESS IN NEUROBIOLOGY, 1998, 54 (05) :531-548
[9]   A functional MRI study of subjects recovered from hemiparetic stroke [J].
Cramer, SC ;
Nelles, G ;
Benson, RR ;
Kaplan, JD ;
Parker, RA ;
Kwong, KK ;
Kennedy, DN ;
Finklestein, SP ;
Rosen, BR .
STROKE, 1997, 28 (12) :2518-2527
[10]   PHOTOCHEMICAL STROKE MODEL - FLUNARIZINE PREVENTS SENSORIMOTOR DEFICITS AFTER NEOCORTICAL INFARCTS IN RATS [J].
DERYCK, M ;
VANREEMPTS, J ;
BORGERS, M ;
WAUQUIER, A ;
JANSSEN, PAJ .
STROKE, 1989, 20 (10) :1383-1390