The mGluR5 negative allosteric modulator dipraglurant reduces dyskinesia in the MPTP macaque model.
Identifieur interne : 000390 ( Main/Exploration ); précédent : 000389; suivant : 000391The mGluR5 negative allosteric modulator dipraglurant reduces dyskinesia in the MPTP macaque model.
Auteurs : Erwan Bezard [République populaire de Chine] ; Elsa Y. Pioli ; Qin Li ; Françoise Girard ; Vincent Mutel ; Charlotte Keywood ; Francois Tison ; Olivier Rascol ; Sonia M. PoliSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2014.
English descriptors
- KwdEn :
- Analysis of Variance, Animals, Antiparkinson Agents (adverse effects), Disease Models, Animal, Dose-Response Relationship, Drug, Dyskinesia, Drug-Induced (blood), Dyskinesia, Drug-Induced (drug therapy), Excitatory Amino Acid Antagonists (blood), Excitatory Amino Acid Antagonists (chemistry), Excitatory Amino Acid Antagonists (therapeutic use), Imidazoles (pharmacology), Imidazoles (therapeutic use), Levodopa (adverse effects), MPTP Poisoning (drug therapy), Macaca mulatta, Male, Motor Activity (drug effects), Pyridines (pharmacology), Pyridines (therapeutic use), Receptor, Metabotropic Glutamate 5 (metabolism), Severity of Illness Index, Time Factors.
- MESH :
- chemical , adverse effects : Antiparkinson Agents, Levodopa.
- blood : Dyskinesia, Drug-Induced, Excitatory Amino Acid Antagonists.
- chemical , chemistry : Excitatory Amino Acid Antagonists.
- drug effects : Motor Activity.
- drug therapy : Dyskinesia, Drug-Induced, MPTP Poisoning.
- chemical , metabolism : Receptor, Metabotropic Glutamate 5.
- chemical , pharmacology : Imidazoles, Pyridines.
- chemical , therapeutic use : Excitatory Amino Acid Antagonists, Imidazoles, Pyridines.
- Analysis of Variance, Animals, Disease Models, Animal, Dose-Response Relationship, Drug, Macaca mulatta, Male, Severity of Illness Index, Time Factors.
Abstract
Blocking metabotropic glutamate receptor type 5 (mGluR5) has been proposed as a target for levodopa-induced dyskinesias (LID) in Parkinson's disease (PD). We assessed the effect on LID of dipraglurant, a potent selective mGluR5 receptor negative allosteric modulator in the gold-standard LID macaque model.
DOI: 10.1002/mds.25920
PubMed: 24865335
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Blocking metabotropic glutamate receptor type 5 (mGluR5) has been proposed as a target for levodopa-induced dyskinesias (LID) in Parkinson's disease (PD). We assessed the effect on LID of dipraglurant, a potent selective mGluR5 receptor negative allosteric modulator in the gold-standard LID macaque model.</div>
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<name sortKey="Keywood, Charlotte" sort="Keywood, Charlotte" uniqKey="Keywood C" first="Charlotte" last="Keywood">Charlotte Keywood</name>
<name sortKey="Li, Qin" sort="Li, Qin" uniqKey="Li Q" first="Qin" last="Li">Qin Li</name>
<name sortKey="Mutel, Vincent" sort="Mutel, Vincent" uniqKey="Mutel V" first="Vincent" last="Mutel">Vincent Mutel</name>
<name sortKey="Pioli, Elsa Y" sort="Pioli, Elsa Y" uniqKey="Pioli E" first="Elsa Y" last="Pioli">Elsa Y. Pioli</name>
<name sortKey="Poli, Sonia M" sort="Poli, Sonia M" uniqKey="Poli S" first="Sonia M" last="Poli">Sonia M. Poli</name>
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<country name="République populaire de Chine"><noRegion><name sortKey="Bezard, Erwan" sort="Bezard, Erwan" uniqKey="Bezard E" first="Erwan" last="Bezard">Erwan Bezard</name>
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