Endocannabinoid levels in patients with Parkinson's disease with and without levodopa-induced dyskinesias.


Journal

Journal of neural transmission (Vienna, Austria : 1996)
ISSN: 1435-1463
Titre abrégé: J Neural Transm (Vienna)
Pays: Austria
ID NLM: 9702341

Informations de publication

Date de publication:
10 2020
Historique:
received: 28 06 2020
accepted: 05 08 2020
pubmed: 17 8 2020
medline: 16 10 2021
entrez: 16 8 2020
Statut: ppublish

Résumé

Levodopa-induced dyskinesias (LID) in Parkinson's disease (PD) are frequent complications, and the endocannabinoid system has a role on its pathophysiology. To test the hypothesis that the functioning of the endocannabinoid system would be altered in PD and in LID by measuring plasma and CSF levels of α-N-arachidonoylethanolamine (AEA) and 2-arachidonoyl-glycerol (2-AG) in patients with PD with and without LID and in healthy controls. Blood and CSF samples were collected from 20 healthy controls, 23 patients with PD without LID, and 24 patients with PD with LID. The levels of AEA and 2-AG were measured using a highly sensitive column switching ultrahigh-performance liquid chromatography-tandem mass spectrometry method. When pooled together, patients with PD had lower plasma and CSF levels of 2-AG and higher CSF levels of AEA compared to healthy controls (Mann-Whitney statistics = 303.0, p = 0.02). Patients with PD without LID had lower CSF levels of 2-AG (Kruskal-Wallis statistics = 7.76, p = 0.02) and higher CSF levels of AEA levels than healthy controls (Kruskal-Wallis statistics = 8.81, p = 0.01). The findings suggest that the endocannabinoid system participates in the pathophysiology of PD symptoms, but its role in the pathophysiology of LID is still unclear.

Identifiants

pubmed: 32797288
doi: 10.1007/s00702-020-02240-9
pii: 10.1007/s00702-020-02240-9
doi:

Substances chimiques

Antiparkinson Agents 0
Endocannabinoids 0
Levodopa 46627O600J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1359-1367

Auteurs

Camila Marchioni (C)

School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.

Bruno Lopes Santos-Lobato (BL)

Department of Neuroscience and Behavior, Ribeirão Preto Medical School, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, São Paulo, CEP: 14049-900, Brazil.
Institute of Health Sciences, Federal University of Pará, Belém, Brazil.

Maria Eugênia Costa Queiroz (MEC)

School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Chemistry Department, University of São Paulo, Ribeirão Preto, Brazil.

José Alexandre S Crippa (JAS)

Department of Neuroscience and Behavior, Ribeirão Preto Medical School, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, São Paulo, CEP: 14049-900, Brazil.

Vitor Tumas (V)

Department of Neuroscience and Behavior, Ribeirão Preto Medical School, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, São Paulo, CEP: 14049-900, Brazil. tumasv@fmrp.usp.br.

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Classifications MeSH