6-Hydroxydopamine lesion and levodopa treatment modify the effect of buspirone in the substantia nigra pars reticulata.


Journal

British journal of pharmacology
ISSN: 1476-5381
Titre abrégé: Br J Pharmacol
Pays: England
ID NLM: 7502536

Informations de publication

Date de publication:
09 2020
Historique:
received: 18 12 2019
revised: 08 05 2020
accepted: 11 05 2020
pubmed: 29 5 2020
medline: 22 6 2021
entrez: 29 5 2020
Statut: ppublish

Résumé

l-DOPA-induced dyskinesia (LID) is considered a major complication in the treatment of Parkinson's disease (PD). Buspirone (5-HT Buspirone was studied using in vivo single-unit, electrocorticogram, local field potential recordings along with microdialysis and immunohistochemistry in naïve/sham, 6-hydroxydopamine (6-OHDA)-lesioned or 6-OHDA-lesioned and l-DOPA-treated (6-OHDA/l-DOPA) rats. Local buspirone inhibited SNr neuron activity in all groups. However, systemic buspirone reduced burst activity in 6-OHDA-lesioned rats (with or without l-DOPA treatment), whereas 8-OH-DPAT, a full 5-HT The effects of buspirone in SNr are influenced by dopamine loss and l-DOPA treatment. The present results suggest that the regulation of burst activity of the SNr induced by DA loss may be a good target to test new drugs for the treatment of PD and LID.

Sections du résumé

BACKGROUND AND PURPOSE
l-DOPA-induced dyskinesia (LID) is considered a major complication in the treatment of Parkinson's disease (PD). Buspirone (5-HT
EXPERIMENTAL APPROACH
Buspirone was studied using in vivo single-unit, electrocorticogram, local field potential recordings along with microdialysis and immunohistochemistry in naïve/sham, 6-hydroxydopamine (6-OHDA)-lesioned or 6-OHDA-lesioned and l-DOPA-treated (6-OHDA/l-DOPA) rats.
KEY RESULTS
Local buspirone inhibited SNr neuron activity in all groups. However, systemic buspirone reduced burst activity in 6-OHDA-lesioned rats (with or without l-DOPA treatment), whereas 8-OH-DPAT, a full 5-HT
CONCLUSIONS AND IMPLICATIONS
The effects of buspirone in SNr are influenced by dopamine loss and l-DOPA treatment. The present results suggest that the regulation of burst activity of the SNr induced by DA loss may be a good target to test new drugs for the treatment of PD and LID.

Identifiants

pubmed: 32464686
doi: 10.1111/bph.15145
pmc: PMC7429490
doi:

Substances chimiques

Antiparkinson Agents 0
Levodopa 46627O600J
Oxidopamine 8HW4YBZ748
Buspirone TK65WKS8HL
Dopamine VTD58H1Z2X

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3957-3974

Subventions

Organisme : Eusko Jaurlaritza
ID : IT747-13
Organisme : Eusko Jaurlaritza
ID : T747-13
Organisme : Ministerio de Economía y Competitividad
ID : SAF2016-77758-R

Informations de copyright

© 2020 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

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Auteurs

Sergio Vegas-Suárez (S)

Department of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain.
Autonomic and Movement Disorders Unit, Neurodegenerative Diseases, Biocruces Health Research Institute, Barakaldo, Bizkaia, Spain.

Clarissa Anna Pisanò (CA)

Department of Medical Sciences, Section of Pharmacology, University of Ferrara, Ferrara, Italy.
Neuroscience Center and National Institute of Neuroscience, University of Ferrara, Ferrara, Italy.

Catalina Requejo (C)

LaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Spain.

Harkaitz Bengoetxea (H)

LaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Spain.

Jose Vicente Lafuente (JV)

LaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Spain.

Michele Morari (M)

Department of Medical Sciences, Section of Pharmacology, University of Ferrara, Ferrara, Italy.
Neuroscience Center and National Institute of Neuroscience, University of Ferrara, Ferrara, Italy.

Cristina Miguelez (C)

Department of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain.
Autonomic and Movement Disorders Unit, Neurodegenerative Diseases, Biocruces Health Research Institute, Barakaldo, Bizkaia, Spain.

Luisa Ugedo (L)

Department of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain.
Autonomic and Movement Disorders Unit, Neurodegenerative Diseases, Biocruces Health Research Institute, Barakaldo, Bizkaia, Spain.

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