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Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions
Comparatively little is known about how new instrumental actions are encoded in the brain. Using whole-brain c-Fos mapping, we show that neural activity is increased in the anterior dorsolateral striatum (aDLS) of mice that successfully learn a new lever-press response to earn food rewards. Post-lea...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387469/ https://www.ncbi.nlm.nih.gov/pubmed/34433818 http://dx.doi.org/10.1038/s41467-021-25460-3 |
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author | Smith, Alexander C. W. Jonkman, Sietse Difeliceantonio, Alexandra G. O’Connor, Richard M. Ghoshal, Soham Romano, Michael F. Everitt, Barry J. Kenny, Paul J. |
author_facet | Smith, Alexander C. W. Jonkman, Sietse Difeliceantonio, Alexandra G. O’Connor, Richard M. Ghoshal, Soham Romano, Michael F. Everitt, Barry J. Kenny, Paul J. |
author_sort | Smith, Alexander C. W. |
collection | PubMed |
description | Comparatively little is known about how new instrumental actions are encoded in the brain. Using whole-brain c-Fos mapping, we show that neural activity is increased in the anterior dorsolateral striatum (aDLS) of mice that successfully learn a new lever-press response to earn food rewards. Post-learning chemogenetic inhibition of aDLS disrupts consolidation of the new instrumental response. Similarly, post-learning infusion of the protein synthesis inhibitor anisomycin into the aDLS disrupts consolidation of the new response. Activity of D1 receptor-expressing medium spiny neurons (D1-MSNs) increases and D2-MSNs activity decreases in the aDLS during consolidation. Chemogenetic inhibition of D1-MSNs in aDLS disrupts the consolidation process whereas D2-MSN inhibition strengthens consolidation but blocks the expression of previously learned habit-like responses. These findings suggest that D1-MSNs in the aDLS encode new instrumental actions whereas D2-MSNs oppose this new learning and instead promote expression of habitual actions. |
format | Online Article Text |
id | pubmed-8387469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83874692021-09-22 Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions Smith, Alexander C. W. Jonkman, Sietse Difeliceantonio, Alexandra G. O’Connor, Richard M. Ghoshal, Soham Romano, Michael F. Everitt, Barry J. Kenny, Paul J. Nat Commun Article Comparatively little is known about how new instrumental actions are encoded in the brain. Using whole-brain c-Fos mapping, we show that neural activity is increased in the anterior dorsolateral striatum (aDLS) of mice that successfully learn a new lever-press response to earn food rewards. Post-learning chemogenetic inhibition of aDLS disrupts consolidation of the new instrumental response. Similarly, post-learning infusion of the protein synthesis inhibitor anisomycin into the aDLS disrupts consolidation of the new response. Activity of D1 receptor-expressing medium spiny neurons (D1-MSNs) increases and D2-MSNs activity decreases in the aDLS during consolidation. Chemogenetic inhibition of D1-MSNs in aDLS disrupts the consolidation process whereas D2-MSN inhibition strengthens consolidation but blocks the expression of previously learned habit-like responses. These findings suggest that D1-MSNs in the aDLS encode new instrumental actions whereas D2-MSNs oppose this new learning and instead promote expression of habitual actions. Nature Publishing Group UK 2021-08-25 /pmc/articles/PMC8387469/ /pubmed/34433818 http://dx.doi.org/10.1038/s41467-021-25460-3 Text en © The Author(s) 2021 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 Smith, Alexander C. W. Jonkman, Sietse Difeliceantonio, Alexandra G. O’Connor, Richard M. Ghoshal, Soham Romano, Michael F. Everitt, Barry J. Kenny, Paul J. Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions |
title | Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions |
title_full | Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions |
title_fullStr | Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions |
title_full_unstemmed | Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions |
title_short | Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions |
title_sort | opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387469/ https://www.ncbi.nlm.nih.gov/pubmed/34433818 http://dx.doi.org/10.1038/s41467-021-25460-3 |
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