Cargando…

Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making

During decisions, animals balance goal achievement and effort management. Despite physical exercise and fatigue significantly affecting the levels of effort that an animal exerts to obtain a reward, their role in effort-based choice and the underlying neurochemistry are incompletely known. In partic...

Descripción completa

Detalles Bibliográficos
Autores principales: Iodice, Pierpaolo, Ferrante, Claudio, Brunetti, Luigi, Cabib, Simona, Protasi, Feliciano, Walton, Mark E., Pezzulo, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428685/
https://www.ncbi.nlm.nih.gov/pubmed/28373651
http://dx.doi.org/10.1038/s41598-017-00561-6
_version_ 1783235877637455872
author Iodice, Pierpaolo
Ferrante, Claudio
Brunetti, Luigi
Cabib, Simona
Protasi, Feliciano
Walton, Mark E.
Pezzulo, Giovanni
author_facet Iodice, Pierpaolo
Ferrante, Claudio
Brunetti, Luigi
Cabib, Simona
Protasi, Feliciano
Walton, Mark E.
Pezzulo, Giovanni
author_sort Iodice, Pierpaolo
collection PubMed
description During decisions, animals balance goal achievement and effort management. Despite physical exercise and fatigue significantly affecting the levels of effort that an animal exerts to obtain a reward, their role in effort-based choice and the underlying neurochemistry are incompletely known. In particular, it is unclear whether fatigue influences decision (cost-benefit) strategies flexibly or only post-decision action execution and learning. To answer this question, we trained mice on a T-maze task in which they chose between a high-cost, high-reward arm (HR), which included a barrier, and a low-cost, low-reward arm (LR), with no barrier. The animals were parametrically fatigued immediately before the behavioural tasks by running on a treadmill. We report a sharp choice reversal, from the HR to LR arm, at 80% of their peak workload (PW), which was temporary and specific, as the mice returned to choose the HC when the animals were successively tested at 60% PW or in a two-barrier task. These rapid reversals are signatures of flexible choice. We also observed increased subcortical dopamine levels in fatigued mice: a marker of individual bias to use model-based control in humans. Our results indicate that fatigue levels can be incorporated in flexible cost-benefits computations that improve foraging efficiency.
format Online
Article
Text
id pubmed-5428685
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-54286852017-05-15 Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making Iodice, Pierpaolo Ferrante, Claudio Brunetti, Luigi Cabib, Simona Protasi, Feliciano Walton, Mark E. Pezzulo, Giovanni Sci Rep Article During decisions, animals balance goal achievement and effort management. Despite physical exercise and fatigue significantly affecting the levels of effort that an animal exerts to obtain a reward, their role in effort-based choice and the underlying neurochemistry are incompletely known. In particular, it is unclear whether fatigue influences decision (cost-benefit) strategies flexibly or only post-decision action execution and learning. To answer this question, we trained mice on a T-maze task in which they chose between a high-cost, high-reward arm (HR), which included a barrier, and a low-cost, low-reward arm (LR), with no barrier. The animals were parametrically fatigued immediately before the behavioural tasks by running on a treadmill. We report a sharp choice reversal, from the HR to LR arm, at 80% of their peak workload (PW), which was temporary and specific, as the mice returned to choose the HC when the animals were successively tested at 60% PW or in a two-barrier task. These rapid reversals are signatures of flexible choice. We also observed increased subcortical dopamine levels in fatigued mice: a marker of individual bias to use model-based control in humans. Our results indicate that fatigue levels can be incorporated in flexible cost-benefits computations that improve foraging efficiency. Nature Publishing Group UK 2017-04-03 /pmc/articles/PMC5428685/ /pubmed/28373651 http://dx.doi.org/10.1038/s41598-017-00561-6 Text en © The Author(s) 2017 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
Iodice, Pierpaolo
Ferrante, Claudio
Brunetti, Luigi
Cabib, Simona
Protasi, Feliciano
Walton, Mark E.
Pezzulo, Giovanni
Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making
title Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making
title_full Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making
title_fullStr Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making
title_full_unstemmed Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making
title_short Fatigue modulates dopamine availability and promotes flexible choice reversals during decision making
title_sort fatigue modulates dopamine availability and promotes flexible choice reversals during decision making
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428685/
https://www.ncbi.nlm.nih.gov/pubmed/28373651
http://dx.doi.org/10.1038/s41598-017-00561-6
work_keys_str_mv AT iodicepierpaolo fatiguemodulatesdopamineavailabilityandpromotesflexiblechoicereversalsduringdecisionmaking
AT ferranteclaudio fatiguemodulatesdopamineavailabilityandpromotesflexiblechoicereversalsduringdecisionmaking
AT brunettiluigi fatiguemodulatesdopamineavailabilityandpromotesflexiblechoicereversalsduringdecisionmaking
AT cabibsimona fatiguemodulatesdopamineavailabilityandpromotesflexiblechoicereversalsduringdecisionmaking
AT protasifeliciano fatiguemodulatesdopamineavailabilityandpromotesflexiblechoicereversalsduringdecisionmaking
AT waltonmarke fatiguemodulatesdopamineavailabilityandpromotesflexiblechoicereversalsduringdecisionmaking
AT pezzulogiovanni fatiguemodulatesdopamineavailabilityandpromotesflexiblechoicereversalsduringdecisionmaking