Levodopa-induced motor complications are associated with alterations of glutamate receptors in Parkinson's disease

被引:176
作者
Calon, F
Rajput, AH
Hornykiewicz, O
Bédard, PJ
Di Paolo, T
机构
[1] Univ Laval, Ctr Med, Mol Endocrinol & Oncol Res Ctr, CHUL, Ste Foy, PQ G1V 4G2, Canada
[2] Univ Laval, Fac Pharm, Ste Foy, PQ G1K 7P4, Canada
[3] Univ Saskatchewan, Div Neurol, Royal Univ Hosp, Saskatoon, SK, Canada
[4] Univ Vienna, Fac Med, Inst Brain Res, Vienna, Austria
[5] Univ Laval, Dept Med, Quebec City, PQ G1K 7P4, Canada
[6] CHUL, Univ Laval, Ctr Med, Neurosci Res Unit, Quebec City, PQ, Canada
基金
加拿大健康研究院;
关键词
dyskinesia; wearing-off; NMDA; AMPA; NRI; Ro; 25-6981; CGP39653; in situ hybridization; autoradiography;
D O I
10.1016/j.nbd.2003.07.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glutamate receptors were studied in the brains of controls and Parkinson's disease (PD) patients, of which 10 of 14 developed motor complications (dyskinesias and/or wearing-off) following levodopa therapy. I-125-RTI binding to the dopamine transporter and dopamine concentrations show comparable nigrostriatal denervation between the subgroups of PD patients. H-3-Ro 25-6981 binding to the NR1/NR2B NMDA receptor was increased in the putamen of PD patients experiencing motor complications compared to those who did not (+53%) and compared to controls (+18%) whereas binding remained unchanged in the caudate nucleus. 3 H-AMPA binding was increased in the lateral putamen (+23%) of PD patients with motor complications compared to those without whereas it was decreased in the caudate nucleus of the PD patients (-16%) compared to controls. Caudate and putamen H-3-CGP39653 binding to NR1/NR2A NMDA receptor and NR1 subunit mRNA levels measured by in situ hybridization were unchanged in subgroups of PD patients compared to controls. These findings suggest that glutamate receptor supersensitivity in the putamen plays a role in the development of motor complications (both wearing-Off and dyskinesias) following long-term levodopa therapy in PD. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:404 / 416
页数:13
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