Cargando…
Cortical recruitment determines learning dynamics and strategy
Salience is a broad and widely used concept in neuroscience whose neuronal correlates, however, remain elusive. In behavioral conditioning, salience is used to explain various effects, such as stimulus overshadowing, and refers to how fast and strongly a stimulus can be associated with a conditioned...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443669/ https://www.ncbi.nlm.nih.gov/pubmed/30931939 http://dx.doi.org/10.1038/s41467-019-09450-0 |
_version_ | 1783407878513623040 |
---|---|
author | Ceballo, Sebastian Bourg, Jacques Kempf, Alexandre Piwkowska, Zuzanna Daret, Aurélie Pinson, Pierre Deneux, Thomas Rumpel, Simon Bathellier, Brice |
author_facet | Ceballo, Sebastian Bourg, Jacques Kempf, Alexandre Piwkowska, Zuzanna Daret, Aurélie Pinson, Pierre Deneux, Thomas Rumpel, Simon Bathellier, Brice |
author_sort | Ceballo, Sebastian |
collection | PubMed |
description | Salience is a broad and widely used concept in neuroscience whose neuronal correlates, however, remain elusive. In behavioral conditioning, salience is used to explain various effects, such as stimulus overshadowing, and refers to how fast and strongly a stimulus can be associated with a conditioned event. Here, we identify sounds of equal intensity and perceptual detectability, which due to their spectro-temporal content recruit different levels of population activity in mouse auditory cortex. When using these sounds as cues in a Go/NoGo discrimination task, the degree of cortical recruitment matches the salience parameter of a reinforcement learning model used to analyze learning speed. We test an essential prediction of this model by training mice to discriminate light-sculpted optogenetic activity patterns in auditory cortex, and verify that cortical recruitment causally determines association or overshadowing of the stimulus components. This demonstrates that cortical recruitment underlies major aspects of stimulus salience during reinforcement learning. |
format | Online Article Text |
id | pubmed-6443669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64436692019-04-03 Cortical recruitment determines learning dynamics and strategy Ceballo, Sebastian Bourg, Jacques Kempf, Alexandre Piwkowska, Zuzanna Daret, Aurélie Pinson, Pierre Deneux, Thomas Rumpel, Simon Bathellier, Brice Nat Commun Article Salience is a broad and widely used concept in neuroscience whose neuronal correlates, however, remain elusive. In behavioral conditioning, salience is used to explain various effects, such as stimulus overshadowing, and refers to how fast and strongly a stimulus can be associated with a conditioned event. Here, we identify sounds of equal intensity and perceptual detectability, which due to their spectro-temporal content recruit different levels of population activity in mouse auditory cortex. When using these sounds as cues in a Go/NoGo discrimination task, the degree of cortical recruitment matches the salience parameter of a reinforcement learning model used to analyze learning speed. We test an essential prediction of this model by training mice to discriminate light-sculpted optogenetic activity patterns in auditory cortex, and verify that cortical recruitment causally determines association or overshadowing of the stimulus components. This demonstrates that cortical recruitment underlies major aspects of stimulus salience during reinforcement learning. Nature Publishing Group UK 2019-04-01 /pmc/articles/PMC6443669/ /pubmed/30931939 http://dx.doi.org/10.1038/s41467-019-09450-0 Text en © The Author(s) 2019 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 Ceballo, Sebastian Bourg, Jacques Kempf, Alexandre Piwkowska, Zuzanna Daret, Aurélie Pinson, Pierre Deneux, Thomas Rumpel, Simon Bathellier, Brice Cortical recruitment determines learning dynamics and strategy |
title | Cortical recruitment determines learning dynamics and strategy |
title_full | Cortical recruitment determines learning dynamics and strategy |
title_fullStr | Cortical recruitment determines learning dynamics and strategy |
title_full_unstemmed | Cortical recruitment determines learning dynamics and strategy |
title_short | Cortical recruitment determines learning dynamics and strategy |
title_sort | cortical recruitment determines learning dynamics and strategy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443669/ https://www.ncbi.nlm.nih.gov/pubmed/30931939 http://dx.doi.org/10.1038/s41467-019-09450-0 |
work_keys_str_mv | AT ceballosebastian corticalrecruitmentdetermineslearningdynamicsandstrategy AT bourgjacques corticalrecruitmentdetermineslearningdynamicsandstrategy AT kempfalexandre corticalrecruitmentdetermineslearningdynamicsandstrategy AT piwkowskazuzanna corticalrecruitmentdetermineslearningdynamicsandstrategy AT daretaurelie corticalrecruitmentdetermineslearningdynamicsandstrategy AT pinsonpierre corticalrecruitmentdetermineslearningdynamicsandstrategy AT deneuxthomas corticalrecruitmentdetermineslearningdynamicsandstrategy AT rumpelsimon corticalrecruitmentdetermineslearningdynamicsandstrategy AT bathellierbrice corticalrecruitmentdetermineslearningdynamicsandstrategy |