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

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Use of metabotropic glutamate 5-receptor antagonists for treatment of levodopa-induced dyskinesias.

Identifieur interne : 001799 ( Ncbi/Merge ); précédent : 001798; suivant : 001800

Use of metabotropic glutamate 5-receptor antagonists for treatment of levodopa-induced dyskinesias.

Auteurs : Olivier Rascol [France] ; Susan Fox [Canada] ; Fabrizio Gasparini [Suisse] ; Christopher Kenney [États-Unis] ; Thérèse Di Paolo [Canada] ; Baltazar Gomez-Mancilla [Canada]

Source :

RBID : pubmed:24951359

English descriptors

Abstract

Modulation of metabotropic glutamate receptors may be a novel therapeutic approach to manage L-Dopa-induced dyskinesias in patients with Parkinson's disease. This article reviews the rationale for use of metabotropic glutamate 5-receptor antagonists in experimental and clinical L-Dopa-induced dyskinesias.

DOI: 10.1016/j.parkreldis.2014.05.003
PubMed: 24951359

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pubmed:24951359

Le document en format XML

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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Modulation of metabotropic glutamate receptors may be a novel therapeutic approach to manage L-Dopa-induced dyskinesias in patients with Parkinson's disease. This article reviews the rationale for use of metabotropic glutamate 5-receptor antagonists in experimental and clinical L-Dopa-induced dyskinesias.</AbstractText>
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<AbstractText Label="RESULTS" NlmCategory="RESULTS">16 preclinical studies of metabotropic glutamate 5-receptor antagonists in animal models of L-Dopa-induced dyskinesias and 7 clinical studies in patients with Parkinson's disease and L-Dopa-induced dyskinesias were included. Anti-dyskinetic effects of metabotropic glutamate 5-receptor blockade (MPEP, MTEP, fenobam, or MRZ-8676) were reported in dyskinetic 6-hydroxydopamine-lesioned rats. Studies in MPTP-lesioned non-human primates reported anti-dyskinetic effects of MPEP, MTEP, fenobam and mavoglurant (AFQ056). Three randomized, double-blind clinical trials reported anti-dyskinetic efficacy of mavoglurant, without effects on anti-parkinsonian therapy, with dizziness the most common adverse event. However, two further studies failed to demonstrate significant anti-dyskinetic efficacy. A randomized, double-blind, placebo-controlled safety study of dipraglurant (ADX48621) demonstrated tolerability and positive exploratory secondary outcomes of reduced dyskinesia.</AbstractText>
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Data generation: Thu May 4 22:20:19 2017. Site generation: Fri Dec 23 23:17:26 2022