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Dopamine transients do not act as model-free prediction errors during associative learning
Dopamine neurons are proposed to signal the reward prediction error in model-free reinforcement learning algorithms. This term represents the unpredicted or ‘excess’ value of the rewarding event, value that is then added to the intrinsic value of any antecedent cues, contexts or events. To support t...
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/PMC6949299/ https://www.ncbi.nlm.nih.gov/pubmed/31913274 http://dx.doi.org/10.1038/s41467-019-13953-1 |
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author | Sharpe, Melissa J. Batchelor, Hannah M. Mueller, Lauren E. Yun Chang, Chun Maes, Etienne J. P. Niv, Yael Schoenbaum, Geoffrey |
author_facet | Sharpe, Melissa J. Batchelor, Hannah M. Mueller, Lauren E. Yun Chang, Chun Maes, Etienne J. P. Niv, Yael Schoenbaum, Geoffrey |
author_sort | Sharpe, Melissa J. |
collection | PubMed |
description | Dopamine neurons are proposed to signal the reward prediction error in model-free reinforcement learning algorithms. This term represents the unpredicted or ‘excess’ value of the rewarding event, value that is then added to the intrinsic value of any antecedent cues, contexts or events. To support this proposal, proponents cite evidence that artificially-induced dopamine transients cause lasting changes in behavior. Yet these studies do not generally assess learning under conditions where an endogenous prediction error would occur. Here, to address this, we conducted three experiments where we optogenetically activated dopamine neurons while rats were learning associative relationships, both with and without reward. In each experiment, the antecedent cues failed to acquire value and instead entered into associations with the later events, whether valueless cues or valued rewards. These results show that in learning situations appropriate for the appearance of a prediction error, dopamine transients support associative, rather than model-free, learning. |
format | Online Article Text |
id | pubmed-6949299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69492992020-01-10 Dopamine transients do not act as model-free prediction errors during associative learning Sharpe, Melissa J. Batchelor, Hannah M. Mueller, Lauren E. Yun Chang, Chun Maes, Etienne J. P. Niv, Yael Schoenbaum, Geoffrey Nat Commun Article Dopamine neurons are proposed to signal the reward prediction error in model-free reinforcement learning algorithms. This term represents the unpredicted or ‘excess’ value of the rewarding event, value that is then added to the intrinsic value of any antecedent cues, contexts or events. To support this proposal, proponents cite evidence that artificially-induced dopamine transients cause lasting changes in behavior. Yet these studies do not generally assess learning under conditions where an endogenous prediction error would occur. Here, to address this, we conducted three experiments where we optogenetically activated dopamine neurons while rats were learning associative relationships, both with and without reward. In each experiment, the antecedent cues failed to acquire value and instead entered into associations with the later events, whether valueless cues or valued rewards. These results show that in learning situations appropriate for the appearance of a prediction error, dopamine transients support associative, rather than model-free, learning. Nature Publishing Group UK 2020-01-08 /pmc/articles/PMC6949299/ /pubmed/31913274 http://dx.doi.org/10.1038/s41467-019-13953-1 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 Sharpe, Melissa J. Batchelor, Hannah M. Mueller, Lauren E. Yun Chang, Chun Maes, Etienne J. P. Niv, Yael Schoenbaum, Geoffrey Dopamine transients do not act as model-free prediction errors during associative learning |
title | Dopamine transients do not act as model-free prediction errors during associative learning |
title_full | Dopamine transients do not act as model-free prediction errors during associative learning |
title_fullStr | Dopamine transients do not act as model-free prediction errors during associative learning |
title_full_unstemmed | Dopamine transients do not act as model-free prediction errors during associative learning |
title_short | Dopamine transients do not act as model-free prediction errors during associative learning |
title_sort | dopamine transients do not act as model-free prediction errors during associative learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949299/ https://www.ncbi.nlm.nih.gov/pubmed/31913274 http://dx.doi.org/10.1038/s41467-019-13953-1 |
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