Excessive daytime sleepiness in a model of Parkinson's disease improved by low-frequency stimulation of the pedunculopontine nucleus.


Journal

NPJ Parkinson's disease
ISSN: 2373-8057
Titre abrégé: NPJ Parkinsons Dis
Pays: United States
ID NLM: 101675390

Informations de publication

Date de publication:
25 Jan 2023
Historique:
received: 24 08 2022
accepted: 12 01 2023
entrez: 25 1 2023
pubmed: 26 1 2023
medline: 26 1 2023
Statut: epublish

Résumé

Patients with Parkinson's disease often complain of excessive daytime sleepiness which negatively impacts their quality of life. The pedunculopontine nucleus, proposed as a target for deep brain stimulation to improve freezing of gait in Parkinson's disease, is also known to play a key role in the arousal system. Thus, the putative control of excessive daytime sleepiness by pedunculopontine nucleus area stimulation merits exploration for treating Parkinson's disease patients. To this end, two adult nonhuman primates (macaca fascicularis) received a deep brain stimulation electrode implanted into the pedunculopontine nucleus area along with a polysomnographic equipment. Stimulation at low frequencies and high frequencies was studied, in healthy and then MPTP-treated nonhuman primates. Here, we observed that MPTP-treated nonhuman primates suffered from excessive daytime sleepiness and that low-frequency stimulation of the pedunculopontine nucleus area was effective in reducing daytime sleepiness. Indeed, low-frequency stimulation of the pedunculopontine nucleus area induced a significant increase in sleep onset latency, longer continuous periods of wakefulness and thus, a partially restored daytime wake architecture. These findings may contribute to the development of new therapeutic strategies in patients suffering from excessive daytime sleepiness.

Identifiants

pubmed: 36697421
doi: 10.1038/s41531-023-00455-7
pii: 10.1038/s41531-023-00455-7
pmc: PMC9876933
doi:

Types de publication

Journal Article

Langues

eng

Pagination

9

Subventions

Organisme : NIH HHS
ID : P51 OD011132
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Aurélie Davin (A)

Univ. Grenoble Alpes, CEA, LETI, Clinatec, 38000, Grenoble, France.
Univ. Grenoble Alpes, Inserm, U1216, Grenoble Institut Neurosciences, 38000, Grenoble, France.

Stéphan Chabardès (S)

Univ. Grenoble Alpes, CEA, LETI, Clinatec, 38000, Grenoble, France.
Univ. Grenoble Alpes, Inserm, U1216, Grenoble Institut Neurosciences, 38000, Grenoble, France.
Univ. Grenoble Alpes, Inserm, Department of Neurosurgery, 38000, Grenoble, France.

Annaelle Devergnas (A)

Yerkes National Primate Research Center, 30307, Atlanta, USA.
Emory University School of Medicine, 30307, Atlanta, GA, USA.

Caroline Benstaali (C)

Univ. Grenoble Alpes, Inserm, U1216, Grenoble Institut Neurosciences, 38000, Grenoble, France.

Claire-Anne N Gutekunst (CN)

Emory University School of Medicine, 30307, Atlanta, GA, USA.

Olivier David (O)

Univ. Grenoble Alpes, Inserm, U1216, Grenoble Institut Neurosciences, 38000, Grenoble, France.
Univ. Aix Marseille, Inserm, INS, Institut de Neurosciences des Systèmes, 13000, Marseille, France.

Napoléon Torres-Martinez (N)

Univ. Grenoble Alpes, CEA, LETI, Clinatec, 38000, Grenoble, France.

Brigitte Piallat (B)

Univ. Grenoble Alpes, Inserm, U1216, Grenoble Institut Neurosciences, 38000, Grenoble, France. brigitte.piallat@univ-grenoble-alpes.fr.

Classifications MeSH