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Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task

Methylphenidate (MPH) is a dopamine transporter (DAT) inhibitor used to treat attention-deficit/hyperactivity-disorder (ADHD). ADHD patients make impulsive choices in delay discounting tasks (DDT) and MPH reduces such impulsivity, but its therapeutic site of action remains unknown. Based on the high...

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Autores principales: Martinez, Eva, Pasquereau, Benjamin, Drui, Guillaume, Saga, Yosuke, Météreau, Élise, Tremblay, Léon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971276/
https://www.ncbi.nlm.nih.gov/pubmed/31959838
http://dx.doi.org/10.1038/s41598-020-57595-6
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author Martinez, Eva
Pasquereau, Benjamin
Drui, Guillaume
Saga, Yosuke
Météreau, Élise
Tremblay, Léon
author_facet Martinez, Eva
Pasquereau, Benjamin
Drui, Guillaume
Saga, Yosuke
Météreau, Élise
Tremblay, Léon
author_sort Martinez, Eva
collection PubMed
description Methylphenidate (MPH) is a dopamine transporter (DAT) inhibitor used to treat attention-deficit/hyperactivity-disorder (ADHD). ADHD patients make impulsive choices in delay discounting tasks (DDT) and MPH reduces such impulsivity, but its therapeutic site of action remains unknown. Based on the high density of DAT in the striatum, we hypothesized that the striatum, especially the ventral striatum (VS) and caudate nucleus which both encode temporal discounting, can be preferential MPH action sites. To determine whether one of these striatal territories is predominantly involved in the effect of MPH, we trained monkeys to make choices during DDT. First, consistent with clinical observations, we found an overall reduction of impulsive choices with a low dose of MPH administered via intramuscular injections, whereas we reported sedative-like effects with a higher dose. Then, using PET-imaging, we found that the therapeutic reduction of impulsive choices was associated with selective DAT occupancy of MPH in the VS. Finally, we confirmed the selective involvement of the VS in the effect of MPH by testing the animals’ impulsivity with microinjections of the drug in distinct striatal territories. Together, these results show that the therapeutic effect of MPH on impulsive decisions is mainly restricted to its action in the VS.
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spelling pubmed-69712762020-01-27 Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task Martinez, Eva Pasquereau, Benjamin Drui, Guillaume Saga, Yosuke Météreau, Élise Tremblay, Léon Sci Rep Article Methylphenidate (MPH) is a dopamine transporter (DAT) inhibitor used to treat attention-deficit/hyperactivity-disorder (ADHD). ADHD patients make impulsive choices in delay discounting tasks (DDT) and MPH reduces such impulsivity, but its therapeutic site of action remains unknown. Based on the high density of DAT in the striatum, we hypothesized that the striatum, especially the ventral striatum (VS) and caudate nucleus which both encode temporal discounting, can be preferential MPH action sites. To determine whether one of these striatal territories is predominantly involved in the effect of MPH, we trained monkeys to make choices during DDT. First, consistent with clinical observations, we found an overall reduction of impulsive choices with a low dose of MPH administered via intramuscular injections, whereas we reported sedative-like effects with a higher dose. Then, using PET-imaging, we found that the therapeutic reduction of impulsive choices was associated with selective DAT occupancy of MPH in the VS. Finally, we confirmed the selective involvement of the VS in the effect of MPH by testing the animals’ impulsivity with microinjections of the drug in distinct striatal territories. Together, these results show that the therapeutic effect of MPH on impulsive decisions is mainly restricted to its action in the VS. Nature Publishing Group UK 2020-01-20 /pmc/articles/PMC6971276/ /pubmed/31959838 http://dx.doi.org/10.1038/s41598-020-57595-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Martinez, Eva
Pasquereau, Benjamin
Drui, Guillaume
Saga, Yosuke
Météreau, Élise
Tremblay, Léon
Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task
title Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task
title_full Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task
title_fullStr Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task
title_full_unstemmed Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task
title_short Ventral striatum supports Methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task
title_sort ventral striatum supports methylphenidate therapeutic effects on impulsive choices expressed in temporal discounting task
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971276/
https://www.ncbi.nlm.nih.gov/pubmed/31959838
http://dx.doi.org/10.1038/s41598-020-57595-6
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