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Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats

Goal‐directed motivated behaviour is crucial for everyday life. Such behaviour is often measured, in rodents, under a progressive ratio (PR) schedule of reinforcement. Previous studies have identified a few brain structures critical for supporting PR performance. However, the association between neu...

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Autores principales: Hailwood, Jonathan M., Gilmour, Gary, Robbins, Trevor W., Saksida, Lisa M., Bussey, Timothy J., Marston, Hugh M., Gastambide, Francois
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282581/
https://www.ncbi.nlm.nih.gov/pubmed/30218588
http://dx.doi.org/10.1111/ejn.14150
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author Hailwood, Jonathan M.
Gilmour, Gary
Robbins, Trevor W.
Saksida, Lisa M.
Bussey, Timothy J.
Marston, Hugh M.
Gastambide, Francois
author_facet Hailwood, Jonathan M.
Gilmour, Gary
Robbins, Trevor W.
Saksida, Lisa M.
Bussey, Timothy J.
Marston, Hugh M.
Gastambide, Francois
author_sort Hailwood, Jonathan M.
collection PubMed
description Goal‐directed motivated behaviour is crucial for everyday life. Such behaviour is often measured, in rodents, under a progressive ratio (PR) schedule of reinforcement. Previous studies have identified a few brain structures critical for supporting PR performance. However, the association between neural activity within these regions and individual differences in effort‐related behaviour is not known. Presently, we used constant potential in vivo oxygen amperometry, a surrogate for functional resonance imaging in rodents, to assess changes in tissue oxygen levels within the nucleus accumbens (NAc) and orbitofrontal cortex (OFC) in male Wistar rats performing a PR task. Within both regions, oxygen responses to rewards increased as the effort exerted to obtain the rewards was larger. Furthermore, higher individual breakpoints were associated with greater magnitude NAc oxygen responses. This association could not be explained by temporal confounds and remained significant when controlling for the different number of completed trials. Animals with higher breakpoints also showed greater magnitude NAc oxygen responses to rewards delivered independently of any behaviour. In contrast, OFC oxygen responses were not associated with individual differences in behavioural performance. The present results suggest that greater NAc oxygen responses following rewards, through a process of incentive motivation, may allow organisms to remain on task for longer and to overcome greater effort costs.
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spelling pubmed-62825812018-12-11 Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats Hailwood, Jonathan M. Gilmour, Gary Robbins, Trevor W. Saksida, Lisa M. Bussey, Timothy J. Marston, Hugh M. Gastambide, Francois Eur J Neurosci Behavioural Neuroscience Goal‐directed motivated behaviour is crucial for everyday life. Such behaviour is often measured, in rodents, under a progressive ratio (PR) schedule of reinforcement. Previous studies have identified a few brain structures critical for supporting PR performance. However, the association between neural activity within these regions and individual differences in effort‐related behaviour is not known. Presently, we used constant potential in vivo oxygen amperometry, a surrogate for functional resonance imaging in rodents, to assess changes in tissue oxygen levels within the nucleus accumbens (NAc) and orbitofrontal cortex (OFC) in male Wistar rats performing a PR task. Within both regions, oxygen responses to rewards increased as the effort exerted to obtain the rewards was larger. Furthermore, higher individual breakpoints were associated with greater magnitude NAc oxygen responses. This association could not be explained by temporal confounds and remained significant when controlling for the different number of completed trials. Animals with higher breakpoints also showed greater magnitude NAc oxygen responses to rewards delivered independently of any behaviour. In contrast, OFC oxygen responses were not associated with individual differences in behavioural performance. The present results suggest that greater NAc oxygen responses following rewards, through a process of incentive motivation, may allow organisms to remain on task for longer and to overcome greater effort costs. John Wiley and Sons Inc. 2018-09-28 2018-11 /pmc/articles/PMC6282581/ /pubmed/30218588 http://dx.doi.org/10.1111/ejn.14150 Text en © 2018 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Behavioural Neuroscience
Hailwood, Jonathan M.
Gilmour, Gary
Robbins, Trevor W.
Saksida, Lisa M.
Bussey, Timothy J.
Marston, Hugh M.
Gastambide, Francois
Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats
title Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats
title_full Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats
title_fullStr Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats
title_full_unstemmed Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats
title_short Oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats
title_sort oxygen responses within the nucleus accumbens are associated with individual differences in effort exertion in rats
topic Behavioural Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282581/
https://www.ncbi.nlm.nih.gov/pubmed/30218588
http://dx.doi.org/10.1111/ejn.14150
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