An enquiry to the role of CB1 receptors in neurodegeneration.


Journal

Neurobiology of disease
ISSN: 1095-953X
Titre abrégé: Neurobiol Dis
Pays: United States
ID NLM: 9500169

Informations de publication

Date de publication:
08 2023
Historique:
received: 03 04 2023
revised: 27 06 2023
accepted: 20 07 2023
medline: 7 8 2023
pubmed: 23 7 2023
entrez: 22 7 2023
Statut: ppublish

Résumé

Neurodegenerative disorders are debilitating conditions that impair patient quality of life and that represent heavy social-economic burdens to society. Whereas the root of some of these brain illnesses lies in autosomal inheritance, the origin of most of these neuropathologies is scantly understood. Similarly, the cellular and molecular substrates explaining the progressive loss of brain functions remains to be fully described too. Indeed, the study of brain neurodegeneration has resulted in a complex picture, composed of a myriad of altered processes that include broken brain bioenergetics, widespread neuroinflammation and aberrant activity of signaling pathways. In this context, several lines of research have shown that the endocannabinoid system (ECS) and its main signaling hub, the type-1 cannabinoid (CB1) receptor are altered in diverse neurodegenerative disorders. However, some of these data are conflictive or poorly described. In this review, we summarize the findings about the alterations in ECS and CB1 receptors signaling in three representative brain illnesses, the Alzheimer's, Parkinson's and Huntington's diseases, and we discuss the relevance of these studies in understanding neurodegeneration development and progression, with a special focus on astrocyte function. Noteworthy, the analysis of ECS defects in neurodegeneration warrant much more studies, as our conceptual understanding of ECS function has evolved quickly in the last years, which now include glia cells and the subcellular-specific CB1 receptors signaling as critical players of brain functions.

Identifiants

pubmed: 37481040
pii: S0969-9961(23)00250-4
doi: 10.1016/j.nbd.2023.106235
pii:
doi:

Substances chimiques

Receptor, Cannabinoid, CB1 0
Endocannabinoids 0
Cannabinoids 0
Receptors, Cannabinoid 0

Types de publication

Review Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106235

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that there are no competing interests associated with the manuscript.

Auteurs

Ignacio Fernández-Moncada (I)

Université de Bordeaux, INSERM, Neurocentre Magendie, U1215, F-33000 Bordeaux, France. Electronic address: ignacio.fernandez-moncada@inserm.fr.

Abel Eraso-Pichot (A)

Université de Bordeaux, INSERM, Neurocentre Magendie, U1215, F-33000 Bordeaux, France.

Tommaso Dalla Tor (T)

Université de Bordeaux, INSERM, Neurocentre Magendie, U1215, F-33000 Bordeaux, France; Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, University of Catania, Catania 95124, Italy.

Bérénice Fortunato-Marsol (B)

Université de Bordeaux, INSERM, Neurocentre Magendie, U1215, F-33000 Bordeaux, France.

Giovanni Marsicano (G)

Université de Bordeaux, INSERM, Neurocentre Magendie, U1215, F-33000 Bordeaux, France. Electronic address: giovanni.marsicano@inserm.fr.

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Classifications MeSH