MK-801 INHIBITS THE INDUCTION OF IMMEDIATE-EARLY GENES IN CEREBRAL-CORTEX, THALAMUS, AND HIPPOCAMPUS, BUT NOT IN SUBSTANTIA-NIGRA FOLLOWING MIDDLE CEREBRAL-ARTERY OCCLUSION
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KINOUCHI, H
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机构:UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
KINOUCHI, H
SHARP, FR
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机构:UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
SHARP, FR
CHAN, PH
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机构:UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
CHAN, PH
MIKAWA, S
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机构:UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
MIKAWA, S
KAMII, H
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机构:UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
KAMII, H
ARAI, S
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机构:UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
ARAI, S
YOSHIMOTO, T
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机构:UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
YOSHIMOTO, T
机构:
[1] UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT NEUROSURG,SAN FRANCISCO,CA 94143
[3] VET AFFAIRS MED CTR,DEPT NEUROL,SAN FRANCISCO,CA
Middle cerebral artery (MCA) occlusion in rats induced c-fos and junB mRN ~ t h later in all ipsilateral cortex outside the MCA distribution and in many subcortical structures: medial striatum; most of thalamus including medial and lateral geniculate nuclei; substantia nigra; and hippocampus. The N-methyl-D-aspartate (NMDA) antagonist, MK-801 (4 mg/kg, i.p.) inhibited c-fos and junB mRNA induction in the cortex, striatum, thalamus, and hippocampus but not in the substantia nigra. These data show that c-fos and junB mRNA induction in cortex, striatum, thalamus, hippocampus involves the activation of NMDA receptors whereas different receptors must be implicated in the induction in substantia nigra.