La maladie de Parkinson au Canada (serveur d'exploration)

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Metabotropic glutamate receptor type 5 in levodopa-induced motor complications

Identifieur interne : 000961 ( PascalFrancis/Curation ); précédent : 000960; suivant : 000962

Metabotropic glutamate receptor type 5 in levodopa-induced motor complications

Auteurs : Bazoumana Ouattara [Canada] ; Laurent Gregoire [Canada] ; Marc Morissette [Canada] ; Fabrizio Gasparini [Suisse] ; Ivo Vranesic [Suisse] ; Graeme Bilbe [Suisse] ; Donald R. Johns [Suisse] ; Alex Rajput [Canada] ; Oleh. Hornykiewicz [Autriche] ; Ali H. Rajput [Canada] ; Baltazar Gomez-Mancilla [Suisse] ; Therese Di Paolo [Canada]

Source :

RBID : Pascal:11-0338872

Descripteurs français

English descriptors

Abstract

Metabotropic glutamate receptors type 5 (mGluR5) are implicated in regulation of synaptic plasticity and learning, and were the focus of our investigation in human Parkinson's disease (PD) patients with dyskinesias and wearing-off, and in 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine (MPTP) monkeys with dyskinesias. Using the selective mGluR5 ligand [3H]ABP688 autoradiography, we measured mGluR5 in brain slices from 11 normal and 14 PD patients and from MPTP monkeys, in relation to motor complications (dyskinesias and wearing-off) associated with treatment with L-dopa. In 16 monkeys with a bilateral MPTP lesion and four controls, [3H]ABP688 specific binding was elevated in the striatum of dyskinetic L-dopa-treated MPTP monkeys but not in MPTP monkeys without dyskinesias compared to controls. PD patients with motor complications (either dyskinesias or wearing-off) had higher [3H]ABP688 specific binding compared to those without motor complications and controls in putamen, external and internal globus pallidus. Elevated glutamatergic transmission as measured with increased mGluR5 specific binding was associated with motor complications and its antagonism could be targeted for their treatment.
pA  
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A08 01  1  ENG  @1 Metabotropic glutamate receptor type 5 in levodopa-induced motor complications
A11 01  1    @1 OUATTARA (Bazoumana)
A11 02  1    @1 GREGOIRE (Laurent)
A11 03  1    @1 MORISSETTE (Marc)
A11 04  1    @1 GASPARINI (Fabrizio)
A11 05  1    @1 VRANESIC (Ivo)
A11 06  1    @1 BILBE (Graeme)
A11 07  1    @1 JOHNS (Donald R.)
A11 08  1    @1 RAJPUT (Alex)
A11 09  1    @1 HORNYKIEWICZ (Oleh.)
A11 10  1    @1 RAJPUT (Ali H.)
A11 11  1    @1 GOMEZ-MANCILLA (Baltazar)
A11 12  1    @1 DI PAOLO (Therese)
A14 01      @1 Molecular Endocrinology and Genomic Research Center, Laval University Medical Center (CHUL @2 Quebec (QC) @3 CAN @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 12 aut.
A14 02      @1 Faculty of Pharmacy, Laval University @2 Quebec (QC @3 CAN @Z 1 aut. @Z 12 aut.
A14 03      @1 Neuroscience Research, Novartis Institutes for BioMedical Research @2 4002 Basel @3 CHE @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 11 aut.
A14 04      @1 Division of Neurology, University of Saskatchewan, Royal University Hospital @2 Saskatoon @3 CAN @Z 8 aut. @Z 10 aut. @Z 12 aut.
A14 05      @1 Institute for Brain Research, Faculty of Medicine, University of Vienna @2 Vienna @3 AUT @Z 9 aut.
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A21       @1 2011
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C01 01    ENG  @0 Metabotropic glutamate receptors type 5 (mGluR5) are implicated in regulation of synaptic plasticity and learning, and were the focus of our investigation in human Parkinson's disease (PD) patients with dyskinesias and wearing-off, and in 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine (MPTP) monkeys with dyskinesias. Using the selective mGluR5 ligand [3H]ABP688 autoradiography, we measured mGluR5 in brain slices from 11 normal and 14 PD patients and from MPTP monkeys, in relation to motor complications (dyskinesias and wearing-off) associated with treatment with L-dopa. In 16 monkeys with a bilateral MPTP lesion and four controls, [3H]ABP688 specific binding was elevated in the striatum of dyskinetic L-dopa-treated MPTP monkeys but not in MPTP monkeys without dyskinesias compared to controls. PD patients with motor complications (either dyskinesias or wearing-off) had higher [3H]ABP688 specific binding compared to those without motor complications and controls in putamen, external and internal globus pallidus. Elevated glutamatergic transmission as measured with increased mGluR5 specific binding was associated with motor complications and its antagonism could be targeted for their treatment.
C02 01  X    @0 002A25L
C02 02  X    @0 002B02B06
C03 01  X  FRE  @0 Récepteur métabotropique @5 01
C03 01  X  ENG  @0 Metabotropic receptor @5 01
C03 01  X  SPA  @0 Receptor metabotropico @5 01
C03 02  X  FRE  @0 Récepteur glutamate @5 02
C03 02  X  ENG  @0 Glutamate receptor @5 02
C03 02  X  SPA  @0 Receptor glutámato @5 02
C03 03  X  FRE  @0 Lévodopa @2 NK @2 FR @5 03
C03 03  X  ENG  @0 Levodopa @2 NK @2 FR @5 03
C03 03  X  SPA  @0 Levodopa @2 NK @2 FR @5 03
C03 04  X  FRE  @0 Neurotoxine @5 04
C03 04  X  ENG  @0 Neurotoxin @5 04
C03 04  X  SPA  @0 Neurotoxina @5 04
C03 05  X  FRE  @0 Sénescence @5 05
C03 05  X  ENG  @0 Senescence @5 05
C03 05  X  SPA  @0 Senescencia @5 05
C03 06  X  FRE  @0 Homme @5 54
C03 06  X  ENG  @0 Human @5 54
C03 06  X  SPA  @0 Hombre @5 54
C03 07  X  FRE  @0 Singe @5 55
C03 07  X  ENG  @0 Monkey @5 55
C03 07  X  SPA  @0 Mono @5 55
C03 08  X  FRE  @0 MPTP @4 INC @5 78
C07 01  X  FRE  @0 Toxine
C07 01  X  ENG  @0 Toxin
C07 01  X  SPA  @0 Toxina
C07 02  X  FRE  @0 Antiparkinsonien @5 20
C07 02  X  ENG  @0 Antiparkinson agent @5 20
C07 02  X  SPA  @0 Antiparkinsoniano @5 20
C07 03  X  FRE  @0 Primates @2 NS
C07 03  X  ENG  @0 Primates @2 NS
C07 03  X  SPA  @0 Primates @2 NS
C07 04  X  FRE  @0 Mammalia @2 NS
C07 04  X  ENG  @0 Mammalia @2 NS
C07 04  X  SPA  @0 Mammalia @2 NS
C07 05  X  FRE  @0 Vertebrata @2 NS
C07 05  X  ENG  @0 Vertebrata @2 NS
C07 05  X  SPA  @0 Vertebrata @2 NS
N21       @1 234
N44 01      @1 OTO
N82       @1 OTO

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Pascal:11-0338872

Le document en format XML

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<title xml:lang="en" level="a">Metabotropic glutamate receptor type 5 in levodopa-induced motor complications</title>
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<name sortKey="Bilbe, Graeme" sort="Bilbe, Graeme" uniqKey="Bilbe G" first="Graeme" last="Bilbe">Graeme Bilbe</name>
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<name sortKey="Johns, Donald R" sort="Johns, Donald R" uniqKey="Johns D" first="Donald R." last="Johns">Donald R. Johns</name>
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<name sortKey="Rajput, Alex" sort="Rajput, Alex" uniqKey="Rajput A" first="Alex" last="Rajput">Alex Rajput</name>
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<s1>Division of Neurology, University of Saskatchewan, Royal University Hospital</s1>
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<name sortKey="Hornykiewicz, Oleh" sort="Hornykiewicz, Oleh" uniqKey="Hornykiewicz O" first="Oleh." last="Hornykiewicz">Oleh. Hornykiewicz</name>
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<name sortKey="Rajput, Ali H" sort="Rajput, Ali H" uniqKey="Rajput A" first="Ali H." last="Rajput">Ali H. Rajput</name>
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<title level="j" type="main">Neurobiology of aging</title>
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<term>Glutamate receptor</term>
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<term>Levodopa</term>
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<div type="abstract" xml:lang="en">Metabotropic glutamate receptors type 5 (mGluR5) are implicated in regulation of synaptic plasticity and learning, and were the focus of our investigation in human Parkinson's disease (PD) patients with dyskinesias and wearing-off, and in 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine (MPTP) monkeys with dyskinesias. Using the selective mGluR5 ligand [
<sup>3</sup>
H]ABP688 autoradiography, we measured mGluR5 in brain slices from 11 normal and 14 PD patients and from MPTP monkeys, in relation to motor complications (dyskinesias and wearing-off) associated with treatment with
<sub>L</sub>
-dopa. In 16 monkeys with a bilateral MPTP lesion and four controls, [
<sup>3</sup>
H]ABP688 specific binding was elevated in the striatum of dyskinetic
<sub>L</sub>
-dopa-treated MPTP monkeys but not in MPTP monkeys without dyskinesias compared to controls. PD patients with motor complications (either dyskinesias or wearing-off) had higher [
<sup>3</sup>
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