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Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales
Optimal behavior requires interpreting environmental cues that indicate when to perform actions. Dopamine is important for learning about reward-predicting events, but its role in adapting to inhibitory cues is unclear. Here we show that when mice can earn rewards in the absence but not presence of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249893/ https://www.ncbi.nlm.nih.gov/pubmed/35778414 http://dx.doi.org/10.1038/s41467-022-31377-2 |
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author | Kalmbach, Abigail Winiger, Vanessa Jeong, Nuri Asok, Arun Gallistel, Charles R. Balsam, Peter D. Simpson, Eleanor H. |
author_facet | Kalmbach, Abigail Winiger, Vanessa Jeong, Nuri Asok, Arun Gallistel, Charles R. Balsam, Peter D. Simpson, Eleanor H. |
author_sort | Kalmbach, Abigail |
collection | PubMed |
description | Optimal behavior requires interpreting environmental cues that indicate when to perform actions. Dopamine is important for learning about reward-predicting events, but its role in adapting to inhibitory cues is unclear. Here we show that when mice can earn rewards in the absence but not presence of an auditory cue, dopamine level in the ventral striatum accurately reflects reward availability in real-time over a sustained period (80 s). In addition, unpredictable transitions between different states of reward availability are accompanied by rapid (~1–2 s) dopamine transients that deflect negatively at the onset and positively at the offset of the cue. This Dopamine encoding of reward availability and transitions between reward availability states is not dependent on reward or activity evoked dopamine release, appears before mice learn the task and is sensitive to motivational state. Our findings are consistent across different techniques including electrochemical recordings and fiber photometry with genetically encoded optical sensors for calcium and dopamine. |
format | Online Article Text |
id | pubmed-9249893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92498932022-07-03 Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales Kalmbach, Abigail Winiger, Vanessa Jeong, Nuri Asok, Arun Gallistel, Charles R. Balsam, Peter D. Simpson, Eleanor H. Nat Commun Article Optimal behavior requires interpreting environmental cues that indicate when to perform actions. Dopamine is important for learning about reward-predicting events, but its role in adapting to inhibitory cues is unclear. Here we show that when mice can earn rewards in the absence but not presence of an auditory cue, dopamine level in the ventral striatum accurately reflects reward availability in real-time over a sustained period (80 s). In addition, unpredictable transitions between different states of reward availability are accompanied by rapid (~1–2 s) dopamine transients that deflect negatively at the onset and positively at the offset of the cue. This Dopamine encoding of reward availability and transitions between reward availability states is not dependent on reward or activity evoked dopamine release, appears before mice learn the task and is sensitive to motivational state. Our findings are consistent across different techniques including electrochemical recordings and fiber photometry with genetically encoded optical sensors for calcium and dopamine. Nature Publishing Group UK 2022-07-01 /pmc/articles/PMC9249893/ /pubmed/35778414 http://dx.doi.org/10.1038/s41467-022-31377-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kalmbach, Abigail Winiger, Vanessa Jeong, Nuri Asok, Arun Gallistel, Charles R. Balsam, Peter D. Simpson, Eleanor H. Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales |
title | Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales |
title_full | Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales |
title_fullStr | Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales |
title_full_unstemmed | Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales |
title_short | Dopamine encodes real-time reward availability and transitions between reward availability states on different timescales |
title_sort | dopamine encodes real-time reward availability and transitions between reward availability states on different timescales |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249893/ https://www.ncbi.nlm.nih.gov/pubmed/35778414 http://dx.doi.org/10.1038/s41467-022-31377-2 |
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