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Decision-making dynamics are predicted by arousal and uninstructed movements
During sensory-guided behavior, an animal’s decision-making dynamics unfold through sequences of distinct performance states, even while stimulus-reward contingencies remain static. Little is known about the factors that underlie these changes in task performance. We hypothesize that these decision-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081205/ https://www.ncbi.nlm.nih.gov/pubmed/37034793 http://dx.doi.org/10.1101/2023.03.02.530651 |
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author | Hulsey, Daniel Zumwalt, Kevin Mazzucato, Luca McCormick, David A. Jaramillo, Santiago |
author_facet | Hulsey, Daniel Zumwalt, Kevin Mazzucato, Luca McCormick, David A. Jaramillo, Santiago |
author_sort | Hulsey, Daniel |
collection | PubMed |
description | During sensory-guided behavior, an animal’s decision-making dynamics unfold through sequences of distinct performance states, even while stimulus-reward contingencies remain static. Little is known about the factors that underlie these changes in task performance. We hypothesize that these decision-making dynamics can be predicted by externally observable measures, such as uninstructed movements and changes in arousal. Here, combining behavioral experiments in mice with computational modeling, we uncovered lawful relationships between transitions in strategic task performance states and an animal’s arousal and uninstructed movements. Using hidden Markov models applied to behavioral choices during sensory discrimination tasks, we found that animals fluctuate between minutes-long optimal, sub-optimal and disengaged performance states. Optimal state epochs were predicted by intermediate levels, and reduced variability, of pupil diameter, along with reduced variability in face movements and locomotion. Our results demonstrate that externally observable uninstructed behaviors can predict optimal performance states, and suggest mice regulate their arousal during optimal performance. |
format | Online Article Text |
id | pubmed-10081205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100812052023-04-08 Decision-making dynamics are predicted by arousal and uninstructed movements Hulsey, Daniel Zumwalt, Kevin Mazzucato, Luca McCormick, David A. Jaramillo, Santiago bioRxiv Article During sensory-guided behavior, an animal’s decision-making dynamics unfold through sequences of distinct performance states, even while stimulus-reward contingencies remain static. Little is known about the factors that underlie these changes in task performance. We hypothesize that these decision-making dynamics can be predicted by externally observable measures, such as uninstructed movements and changes in arousal. Here, combining behavioral experiments in mice with computational modeling, we uncovered lawful relationships between transitions in strategic task performance states and an animal’s arousal and uninstructed movements. Using hidden Markov models applied to behavioral choices during sensory discrimination tasks, we found that animals fluctuate between minutes-long optimal, sub-optimal and disengaged performance states. Optimal state epochs were predicted by intermediate levels, and reduced variability, of pupil diameter, along with reduced variability in face movements and locomotion. Our results demonstrate that externally observable uninstructed behaviors can predict optimal performance states, and suggest mice regulate their arousal during optimal performance. Cold Spring Harbor Laboratory 2023-03-28 /pmc/articles/PMC10081205/ /pubmed/37034793 http://dx.doi.org/10.1101/2023.03.02.530651 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Hulsey, Daniel Zumwalt, Kevin Mazzucato, Luca McCormick, David A. Jaramillo, Santiago Decision-making dynamics are predicted by arousal and uninstructed movements |
title | Decision-making dynamics are predicted by arousal and uninstructed movements |
title_full | Decision-making dynamics are predicted by arousal and uninstructed movements |
title_fullStr | Decision-making dynamics are predicted by arousal and uninstructed movements |
title_full_unstemmed | Decision-making dynamics are predicted by arousal and uninstructed movements |
title_short | Decision-making dynamics are predicted by arousal and uninstructed movements |
title_sort | decision-making dynamics are predicted by arousal and uninstructed movements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081205/ https://www.ncbi.nlm.nih.gov/pubmed/37034793 http://dx.doi.org/10.1101/2023.03.02.530651 |
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