Stroke, Vol 25, 1855-1860, Copyright © 1994 by American Heart Association
Y Collaco-Moraes, BS Aspey, JS de Belleroche and MJ Harrison
BACKGROUND AND PURPOSE: There is strong evidence to implicate glutamate in
the cerebral damage caused by ischemia. In this study we investigated the
role of glutamate receptors in mediating effects of middle cerebral artery
occlusion (MCAO) on immediate early gene expression in the rat by
quantitation of mRNA levels. METHODS: The effect of MCAO on the induction
of immediate early genes was studied in five regions, both ipsilateral and
contralateral to the occlusion: the "core" ischemic area of the cortex in
the central region of the middle cerebral artery territory, the surrounding
area, frontal cortex, occipital cortex, and hippocampus. Levels of c-fos,
c-jun, zif-268, and krox-20 mRNA were measured by Northern and slot blot
analysis. RESULTS: A large induction of c-fos mRNA was obtained in all four
cortical regions ipsilateral to the occlusion, with the greatest effect
detected in the core area. Little effect was detected in the ipsilateral
hippocampus and in all contralateral regions. Pretreatment with MK-801 (3
mg/kg) largely inhibited the induction of c-fos mRNA, indicating that the
induction was mediated through an N-methyl-D-aspartate subtype of glutamate
receptor. MCAO also produced a significant induction of c- jun and zif-268
mRNA in ipsilateral cortical regions. CONCLUSIONS: These results indicate
that MCAO causes a profound modulation of the expression of multiple genes
in an extensive area of cerebral cortex extending beyond the immediate area
supplied by the middle cerebral artery. The marked effect of MK-801
indicates the potential importance of glutamate antagonists in restricting
the widespread deleterious effects of glutamate.
ARTICLES
Focal ischemia causes an extensive induction of immediate early genes that are sensitive to MK-801
Department of Biochemistry, Charing Cross and Westminster Medical School, London, UK.
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