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The metabotropic excitatory amino acid receptor agonist 1S,3R-ACPD selectively potentiates N-methyl-D-aspartate-induced brain injury.

作者信息

McDonald J W, Schoepp D D

机构信息

CNS Research, Eli Lilly and Company, Indianapolis, IN 46285.

出版信息

Eur J Pharmacol. 1992 May 14;215(2-3):353-4. doi: 10.1016/0014-2999(92)90058-c.

DOI:10.1016/0014-2999(92)90058-c
PMID:1383003
Abstract

The role of metabotropic type excitatory amino acid receptors in brain injury was assessed using the selective metabotropic receptor agonist, (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (1S,3R-ACPD). Intrastriatal stereotaxic injection of 1S,3R-ACPD (250 nmol) in PND 7 rats produced little brain injury as assessed by hemispheric weight disparities. However, 1S,3R-ACPD markedly potentiated N-methyl-D-aspartate (NMDA)-, but not alpha-amino-3-hydroxy-5-methyl-4-isoxazoleproprionic acid (AMPA)-, mediated brain injury. This effect was stereoselective since the inactive metabotropic agonist, 1R,3S-ACPD, did not potentiate NMDA toxicity.

摘要

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