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Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease

Beyond classical motor symptoms, motivational and affective deficits are frequently observed in Parkinson’s disease (PD), dramatically impairing the quality of life of patients. Using bilateral 6-hydroxydopamine (6-OHDA) lesions of the substantia nigra pars compacta (SNc) in rats, we have been able...

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Autores principales: Favier, Mathieu, Carcenac, Carole, Drui, Guillaume, Vachez, Yvan, Boulet, Sabrina, Savasta, Marc, Carnicella, Sebastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278505/
https://www.ncbi.nlm.nih.gov/pubmed/28134302
http://dx.doi.org/10.1038/srep41589
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author Favier, Mathieu
Carcenac, Carole
Drui, Guillaume
Vachez, Yvan
Boulet, Sabrina
Savasta, Marc
Carnicella, Sebastien
author_facet Favier, Mathieu
Carcenac, Carole
Drui, Guillaume
Vachez, Yvan
Boulet, Sabrina
Savasta, Marc
Carnicella, Sebastien
author_sort Favier, Mathieu
collection PubMed
description Beyond classical motor symptoms, motivational and affective deficits are frequently observed in Parkinson’s disease (PD), dramatically impairing the quality of life of patients. Using bilateral 6-hydroxydopamine (6-OHDA) lesions of the substantia nigra pars compacta (SNc) in rats, we have been able to reproduce these neuropsychiatric/non-motor impairments. The present study describes how bilateral 6-OHDA SNc lesions affect the function of the main striatal dopaminergic (DA) receptor subtypes. Autoradiography was used to measure the levels of striatal DA receptors, and operant sucrose self-administration and neuropharmacological approaches were combined to investigate the causal implication of specific DA receptors subtypes in the motivational deficits induced by a dorsostriatal DA denervation. We found that D3 receptors (D(3)R) exclusively are down-regulated within the dorsal striatum of lesioned rats. We next showed that infusion of a D(3)R antagonist (SB-277011A) in non-lesioned animals specifically disrupts preparatory, but not consummatory behaviors. Our findings reveal an unexpected involvement of dorsostriatal D(3)R in motivational processes. They strongly suggest an implication of dorsostriatal D(3)R in the neuropsychiatric symptoms observed in PD, highlighting this receptor as a potential target for pharmacological treatment.
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spelling pubmed-52785052017-02-03 Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease Favier, Mathieu Carcenac, Carole Drui, Guillaume Vachez, Yvan Boulet, Sabrina Savasta, Marc Carnicella, Sebastien Sci Rep Article Beyond classical motor symptoms, motivational and affective deficits are frequently observed in Parkinson’s disease (PD), dramatically impairing the quality of life of patients. Using bilateral 6-hydroxydopamine (6-OHDA) lesions of the substantia nigra pars compacta (SNc) in rats, we have been able to reproduce these neuropsychiatric/non-motor impairments. The present study describes how bilateral 6-OHDA SNc lesions affect the function of the main striatal dopaminergic (DA) receptor subtypes. Autoradiography was used to measure the levels of striatal DA receptors, and operant sucrose self-administration and neuropharmacological approaches were combined to investigate the causal implication of specific DA receptors subtypes in the motivational deficits induced by a dorsostriatal DA denervation. We found that D3 receptors (D(3)R) exclusively are down-regulated within the dorsal striatum of lesioned rats. We next showed that infusion of a D(3)R antagonist (SB-277011A) in non-lesioned animals specifically disrupts preparatory, but not consummatory behaviors. Our findings reveal an unexpected involvement of dorsostriatal D(3)R in motivational processes. They strongly suggest an implication of dorsostriatal D(3)R in the neuropsychiatric symptoms observed in PD, highlighting this receptor as a potential target for pharmacological treatment. Nature Publishing Group 2017-01-30 /pmc/articles/PMC5278505/ /pubmed/28134302 http://dx.doi.org/10.1038/srep41589 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Favier, Mathieu
Carcenac, Carole
Drui, Guillaume
Vachez, Yvan
Boulet, Sabrina
Savasta, Marc
Carnicella, Sebastien
Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease
title Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease
title_full Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease
title_fullStr Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease
title_full_unstemmed Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease
title_short Implication of dorsostriatal D3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in Parkinson’s disease
title_sort implication of dorsostriatal d3 receptors in motivational processes: a potential target for neuropsychiatric symptoms in parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278505/
https://www.ncbi.nlm.nih.gov/pubmed/28134302
http://dx.doi.org/10.1038/srep41589
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