Abstract
The present study shows that systemic administration of the selective, non-competitive N-methyl-D-aspartate antagonist MK-801 [(+)-5-methyl-10,11-dihydroxy-5H-dibenzo (a,d)-cyclohepten-5,10-imine] dose-dependently induces ipsiversive rotational behavior in the rats with a unilateral striatal lesion produced by transient middle cerebral artery occlusion or in those with a unilateral nigrostriatal lesion produced by 6-hydroxydopamaine. In relation to a functional model of the basal ganglia-thalamocortical 'motor' circuit, the present data suggest that the striatum may be one of the most important sites where MK-801 acts in the basal ganglia, with its being responsible for the circling behavior of the animal models.
MeSH Terms
Animals
Dizocilpine Maleate/toxicity
Dose-Response Relationship, Drug
Ischemic Attack, Transient/chemically induced,pathology
Motor Activity/drug effects
Neostriatum/drug effects,pathology
Oxidopamine
Rats
Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors
Stereotyped Behavior/drug effects
Substantia Nigra/drug effects,pathology
Chemicals
Receptors, N-Methyl-D-Aspartate
Dizocilpine Maleate
Oxidopamine
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Goto S
Department of Neurosurgery, Kumamoto University Medical School, Japan.
Korematsu K
Inoue N
Yamada K
Oyama T
Nagahiro S
Ushio Y
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