Cannabinoid type 2 receptor activation inhibits MPP


Journal

Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234

Informations de publication

Date de publication:
May 2023
Historique:
received: 29 10 2022
accepted: 17 03 2023
medline: 1 5 2023
pubmed: 29 3 2023
entrez: 28 3 2023
Statut: ppublish

Résumé

Growing evidence indicates that cannabinoid type 2 (CB2) receptor activation inhibits neuroinflammation in the pathogenesis of Parkinson's disease (PD). Nonetheless, the precise mechanisms of CB2 receptor-mediated neuroprotection have not been fully elucidated. The differentiation of microglia from the M1 to M2 phenotype plays a vital role in neuroinflammation. In the present study, we investigated the effect of CB2 receptor activation on the M1/M2 phenotypic transformation of microglia treated with 1-methyl-4-phenylpyridinium (MPP+). The M1 phenotype microglia markers, including inducible nitric oxide (iNOS), interleukin 6 (IL-6), and CD86, and the M2 phenotype microglia markers, including arginase-1 (Arg-1), IL-10, and CD206, were detected by western blots and flow cytometry. The levels of phosphoinositide-3-kinase (PI3K)/Akt and nuclear factor erythroid 2-related factor 2 (Nrf2) were determined by Western blots. Subsequent addition of Nrf2 inhibitors initially revealed the specific mechanism by which CB2 receptors affect phenotypic changes in microglia. Our results showed that pretreatment with JWH133 significantly inhibited the MPP The results indicate that CB2 receptor activation promotes MPP

Sections du résumé

BACKGROUND BACKGROUND
Growing evidence indicates that cannabinoid type 2 (CB2) receptor activation inhibits neuroinflammation in the pathogenesis of Parkinson's disease (PD). Nonetheless, the precise mechanisms of CB2 receptor-mediated neuroprotection have not been fully elucidated. The differentiation of microglia from the M1 to M2 phenotype plays a vital role in neuroinflammation.
METHODS METHODS
In the present study, we investigated the effect of CB2 receptor activation on the M1/M2 phenotypic transformation of microglia treated with 1-methyl-4-phenylpyridinium (MPP+). The M1 phenotype microglia markers, including inducible nitric oxide (iNOS), interleukin 6 (IL-6), and CD86, and the M2 phenotype microglia markers, including arginase-1 (Arg-1), IL-10, and CD206, were detected by western blots and flow cytometry. The levels of phosphoinositide-3-kinase (PI3K)/Akt and nuclear factor erythroid 2-related factor 2 (Nrf2) were determined by Western blots. Subsequent addition of Nrf2 inhibitors initially revealed the specific mechanism by which CB2 receptors affect phenotypic changes in microglia.
RESULTS RESULTS
Our results showed that pretreatment with JWH133 significantly inhibited the MPP
CONCLUSION CONCLUSIONS
The results indicate that CB2 receptor activation promotes MPP

Identifiants

pubmed: 36977807
doi: 10.1007/s11033-023-08395-4
pii: 10.1007/s11033-023-08395-4
doi:

Substances chimiques

Proto-Oncogene Proteins c-akt EC 2.7.11.1
1,1-dimethylbutyl-1-deoxy-Delta(9)-THC TDG8048RDA
Phosphatidylinositol 3-Kinases EC 2.7.1.-
NF-E2-Related Factor 2 0
1-Methyl-4-phenylpyridinium R865A5OY8J
Phosphatidylinositol 3-Kinase EC 2.7.1.137
Receptor, Cannabinoid, CB2 0
Cannabinoids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4423-4433

Subventions

Organisme : Key Technology Research and Development Program of Shandong
ID : No. 2019GSF108095

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature B.V.

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Auteurs

Mengya Wang (M)

Department of Physiology, School of Basic Medicine, Institute of Brain Science and Disorders, Qingdao University, Qingdao, 266071, China.

Man Liu (M)

Department of Physiology, School of Basic Medicine, Institute of Brain Science and Disorders, Qingdao University, Qingdao, 266071, China.

Zegang Ma (Z)

Department of Physiology, School of Basic Medicine, Institute of Brain Science and Disorders, Qingdao University, Qingdao, 266071, China. mazegang@126.com.

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