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8-hydroxy-2-(di-n-propylamino)tetralin reduces striatal glutamate in an animal model of Parkinson's disease.

作者信息

Mignon Laurence J, Wolf William A

机构信息

Department of Neurology, David Geffen School of Medicine at UCLA, B114 Reed Neurology Research Center, Los Angeles, CA 90095, USA.

出版信息

Neuroreport. 2005 May 12;16(7):699-703. doi: 10.1097/00001756-200505120-00009.

Abstract

Using in-vivo microdialysis, we examined the effect of the serotonin 5-HT1A agonist R-(+)-8-hydroxy-2-(di-n-propylamino)tetralin on striatal extracellular excitatory amino acids in an animal model of Parkinson's disease. Extracellular glutamate and aspartate in the dopamine-denervated striatum of unilateral 6-hydroxydopamine-lesioned rats were significantly decreased by acute subcutaneous injection of R-(+)-8-hydroxy-2-(di-n-propylamino) tetralin (0.3 mg/kg). Although not quantified in the present study, a concomitant increase in locomotor activity was anecdotally observed following R-(+)-8-hydroxy-2-(di-n-propylamino)tetralin. These results suggest that systemic administration of a 5-HT1A agonist can reduce glutamate neurotransmission in the dopamine-denervated striatum. The results are discussed with respect to the treatment of Parkinson's disease.

摘要

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