Striatal AMPA receptor binding is unaltered in the MPTP-lesioned macaque model of Parkinson's disease and dyskinesia

被引:19
作者
Silverdale, MA [1 ]
Crossman, AR [1 ]
Brotchie, JM [1 ]
机构
[1] Manchester Movement Disorders Lab, Manchester, Lancs, England
基金
英国医学研究理事会;
关键词
Parkinson's disease; glutamate; AMPA; MPTP; primate; binding; dyskinesia;
D O I
10.1006/exnr.2001.7854
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Long-term levodopa or dopamine agonist treatment in the MPTP-lesioned primate model of Parkinson's disease elicits dyskinesia, which is phenotypically similar to levodopa-induced dyskinesia in patients with Parkinson's disease. AMPA receptor antagonists have previously been shown to have both anti-parkinsonian and anti-dyskinetic actions in MPTP-lesioned primates, suggesting that AMPA receptor transmission is functionally overactive under these conditions. In this study, we investigated the level of striatal AMPA receptor binding in the MPTP lesioned primate using the selective AMPA ligand H-3-(S)-5-fluorowillardiine. AMPA receptor binding was studied in nonparkinsonian, nondyskinetic parkinsonian, and dyskinetic macaques. Striatal AMPA receptor binding was not different in any of the treatment groups (P > 0.05). Although AMPA receptor-mediated transmission is functionally overactive in Parkinson's disease and dyskinesia, changes in striatal AMPA receptor levels are not likely to be the cause of such movement disorders. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:21 / 28
页数:8
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