Author/Authors :
Pershia Samadi، نويسنده , , Laurent Grégoire، نويسنده , , Marc Morissette، نويسنده , , Frédéric Calon، نويسنده , , Abdallah Hadj Tahar، نويسنده , , Mehdi Dridi، نويسنده , , Nancy Bélanger، نويسنده , , Leonard T. Meltzer، نويسنده , , Paul J. Bédard، نويسنده , , Thérèse di Paolo، نويسنده ,
Abstract :
Modulation of excessive glutamatergic transmission within the basal ganglia is considered as an alternative approach to reduce L-Dopa-induced dyskinesias (LIDs) in Parkinsonʹs disease (PD). In this study receptor binding autoradiography of [3H]MPEP, a metabotropic glutamate receptor 5 (mGluR5) selective radioligand, was used to investigate possible changes in mGluR5 in the basal ganglia of L-Dopa-treated 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) monkeys having developed LIDs compared to animals in which LIDs was prevented by adjunct treatments. LIDs were associated with an increase of mGluR5 specific binding in the posterior putamen and pallidum (+41% and +56%) compared to controls. By contrast, prevention of dyskinesias was associated with an important decrease of mGluR5 specific binding in these areas (−37% and −48%) compared with dyskinetic animals. Moreover, an upregulation (+34%) of mGluR5 receptor binding was seen in the anterior caudate nucleus of saline treated MPTP monkeys. This study is the first to provide evidence that enhanced mGluR5 specific binding in the posterior putamen and pallidum may contribute to the pathogenesis of LIDs in PD.
Keywords :
Basal ganglia , Parkinson’s disease , Dyskinesias , mGluR5 , NMDA antagonist , cabergoline