D1 receptor agonist improves sleep-wake parameters in experimental parkinsonism.
Identifieur interne : 000609 ( PubMed/Corpus ); précédent : 000608; suivant : 000610D1 receptor agonist improves sleep-wake parameters in experimental parkinsonism.
Auteurs : Carole Hyacinthe ; Quentin Barraud ; François Tison ; Erwan Bezard ; Imad GhorayebSource :
- Neurobiology of disease [ 1095-953X ] ; 2014.
English descriptors
- KwdEn :
- 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine (therapeutic use), Analysis of Variance, Animals, Disease Models, Animal, Dopamine Agonists (therapeutic use), Dose-Response Relationship, Drug, Electrocardiography, Electroencephalography, Electromyography, Female, Levodopa (therapeutic use), Macaca fascicularis, Macaca mulatta, Parkinsonian Disorders (complications), Parkinsonian Disorders (drug therapy), Quinpirole (therapeutic use), Sleep (drug effects), Sleep Disorders, Circadian Rhythm (drug therapy), Sleep Disorders, Circadian Rhythm (etiology), Telemetry, Time Factors, Wakefulness (drug effects).
- MESH :
- chemical , therapeutic use : 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine, Dopamine Agonists, Levodopa, Quinpirole.
- complications : Parkinsonian Disorders.
- drug effects : Sleep, Wakefulness.
- drug therapy : Parkinsonian Disorders, Sleep Disorders, Circadian Rhythm.
- etiology : Sleep Disorders, Circadian Rhythm.
- Analysis of Variance, Animals, Disease Models, Animal, Dose-Response Relationship, Drug, Electrocardiography, Electroencephalography, Electromyography, Female, Macaca fascicularis, Macaca mulatta, Telemetry, Time Factors.
Abstract
Both excessive daytime sleepiness (EDS) and rapid eye movement (REM) sleep deregulation are part of Parkinson's disease (PD) non-motor symptoms and may complicate dopamine replacement therapy. We report here that dopamine agonists act differentially on sleep architecture in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine macaque monkey. Continuous sleep and wake electroencephalographic monitoring revealed no effect of the selective dopamine D2 receptor agonist quinpirole on EDS, whereas the selective dopamine D1 receptor agonist SKF38393 efficiently alleviated EDS and restored REM sleep to baseline values. The present results question the relevance of abandoning D1 receptor agonist treatment in PD as it might actually improve sleep-related disorders.
DOI: 10.1016/j.nbd.2013.10.029
PubMed: 24211719
Links to Exploration step
pubmed:24211719Le document en format XML
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<author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name>
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<series><title level="j">Neurobiology of disease</title>
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<term>Animals</term>
<term>Disease Models, Animal</term>
<term>Dopamine Agonists (therapeutic use)</term>
<term>Dose-Response Relationship, Drug</term>
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<front><div type="abstract" xml:lang="en">Both excessive daytime sleepiness (EDS) and rapid eye movement (REM) sleep deregulation are part of Parkinson's disease (PD) non-motor symptoms and may complicate dopamine replacement therapy. We report here that dopamine agonists act differentially on sleep architecture in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine macaque monkey. Continuous sleep and wake electroencephalographic monitoring revealed no effect of the selective dopamine D2 receptor agonist quinpirole on EDS, whereas the selective dopamine D1 receptor agonist SKF38393 efficiently alleviated EDS and restored REM sleep to baseline values. The present results question the relevance of abandoning D1 receptor agonist treatment in PD as it might actually improve sleep-related disorders.</div>
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<Abstract><AbstractText>Both excessive daytime sleepiness (EDS) and rapid eye movement (REM) sleep deregulation are part of Parkinson's disease (PD) non-motor symptoms and may complicate dopamine replacement therapy. We report here that dopamine agonists act differentially on sleep architecture in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine macaque monkey. Continuous sleep and wake electroencephalographic monitoring revealed no effect of the selective dopamine D2 receptor agonist quinpirole on EDS, whereas the selective dopamine D1 receptor agonist SKF38393 efficiently alleviated EDS and restored REM sleep to baseline values. The present results question the relevance of abandoning D1 receptor agonist treatment in PD as it might actually improve sleep-related disorders.</AbstractText>
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