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Movement errors during skilled motor performance engage distinct prediction error mechanisms
The brain detects deviations from intended behaviors by estimating the mismatch between predicted and actual outcomes. Axiomatic to these computations are salience and valence prediction error signals, which alert the brain to the occurrence and value of unexpected events. Despite the theoretical as...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732826/ https://www.ncbi.nlm.nih.gov/pubmed/33311566 http://dx.doi.org/10.1038/s42003-020-01465-4 |
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author | Gabitov, Ella Lungu, Ovidiu Albouy, Geneviève Doyon, Julien |
author_facet | Gabitov, Ella Lungu, Ovidiu Albouy, Geneviève Doyon, Julien |
author_sort | Gabitov, Ella |
collection | PubMed |
description | The brain detects deviations from intended behaviors by estimating the mismatch between predicted and actual outcomes. Axiomatic to these computations are salience and valence prediction error signals, which alert the brain to the occurrence and value of unexpected events. Despite the theoretical assertion of these prediction error signals, it is unknown whether and how brain mechanisms underlying their computations support error processing during skilled motor behavior. Here we demonstrate, with functional magnetic resonance imaging, that internal detection, i.e., without externally-provided feedback, of self-generated movement errors evokes instantaneous activity increases within the salience network and delayed lingering decreases within the nucleus accumbens – a key structure in the reward valuation pathway. A widespread suppression within the sensorimotor network was also observed. Our findings suggest that neural computations of salience and valence prediction errors during skilled motor behaviors operate on different time-scales and, therefore, may contribute differentially to immediate and longer-term adaptive processes. |
format | Online Article Text |
id | pubmed-7732826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77328262020-12-17 Movement errors during skilled motor performance engage distinct prediction error mechanisms Gabitov, Ella Lungu, Ovidiu Albouy, Geneviève Doyon, Julien Commun Biol Article The brain detects deviations from intended behaviors by estimating the mismatch between predicted and actual outcomes. Axiomatic to these computations are salience and valence prediction error signals, which alert the brain to the occurrence and value of unexpected events. Despite the theoretical assertion of these prediction error signals, it is unknown whether and how brain mechanisms underlying their computations support error processing during skilled motor behavior. Here we demonstrate, with functional magnetic resonance imaging, that internal detection, i.e., without externally-provided feedback, of self-generated movement errors evokes instantaneous activity increases within the salience network and delayed lingering decreases within the nucleus accumbens – a key structure in the reward valuation pathway. A widespread suppression within the sensorimotor network was also observed. Our findings suggest that neural computations of salience and valence prediction errors during skilled motor behaviors operate on different time-scales and, therefore, may contribute differentially to immediate and longer-term adaptive processes. Nature Publishing Group UK 2020-12-11 /pmc/articles/PMC7732826/ /pubmed/33311566 http://dx.doi.org/10.1038/s42003-020-01465-4 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 Gabitov, Ella Lungu, Ovidiu Albouy, Geneviève Doyon, Julien Movement errors during skilled motor performance engage distinct prediction error mechanisms |
title | Movement errors during skilled motor performance engage distinct prediction error mechanisms |
title_full | Movement errors during skilled motor performance engage distinct prediction error mechanisms |
title_fullStr | Movement errors during skilled motor performance engage distinct prediction error mechanisms |
title_full_unstemmed | Movement errors during skilled motor performance engage distinct prediction error mechanisms |
title_short | Movement errors during skilled motor performance engage distinct prediction error mechanisms |
title_sort | movement errors during skilled motor performance engage distinct prediction error mechanisms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732826/ https://www.ncbi.nlm.nih.gov/pubmed/33311566 http://dx.doi.org/10.1038/s42003-020-01465-4 |
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