Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8516622 | Neuropharmacology | 2018 | 42 Pages |
Abstract
2017 is the 200th anniversary of the first published description of Parkinson's disease (PD). Fifty years ago, the clinical benefit of levodopa was first documented, representing the most important advance in the treatment of PD so far. Among the novel targets identified in the last decade, positive allosteric modulators (PAM) of mGlu4 receptors show great promise, with the potential to change the paradigm of the PD treatment approach. mGlu4 PAMs have shown consistent efficacy in various preclinical models of PD, and entered clinical trials for the first time in 2017. This review synthesizes the rationale for mGlu4 PAM development for PD and progress to date, reporting the key achievements from preclinical studies to the first-in-class compound assessment in man.
Keywords
6-OHDAMSNNHPMOASTNmGluMPTPSubstantia nigra pars reticulatamGlu4l-AP4QOLSNRPAM6-HydroxydopaminePHCCCLIDQuality of life1-methyl-4-phenyl-1,2,3,6-tetrahydropyridineSNpcgamma-aminobutyric acidParkinson's diseasesubstantia nigra pars compactaMode of actionabnormal involuntary movementsDopaminedyskinesiaLevodopa-induced dyskinesiapositive allosteric modulatornegative allosteric modulatorNAMDopamine receptor type 2dopamine receptor type 1AIMSubthalamic nucleusNon-human primatesGABAglutamateMetabotropic glutamate receptor
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Authors
Delphine Charvin,