Decision-making dynamics are predicted by arousal and uninstructed movements

Summary: 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...

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Main Authors: Daniel Hulsey, Kevin Zumwalt, Luca Mazzucato, David A. McCormick, Santiago Jaramillo
Format: Article
Language:English
Published: Elsevier 2024-02-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124724000378
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author Daniel Hulsey
Kevin Zumwalt
Luca Mazzucato
David A. McCormick
Santiago Jaramillo
author_facet Daniel Hulsey
Kevin Zumwalt
Luca Mazzucato
David A. McCormick
Santiago Jaramillo
author_sort Daniel Hulsey
collection DOAJ
description Summary: 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, using computational modeling of visual and auditory task performance data from mice, 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 find that animals fluctuate between minutes-long optimal, sub-optimal, and disengaged performance states. Optimal state epochs are predicted by intermediate levels, and reduced variability, of pupil diameter and movement. Our results demonstrate that externally observable uninstructed behaviors can predict optimal performance states and suggest that mice regulate their arousal during optimal performance.
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spelling doaj.art-40b062e91c56478a91849586b54a09272024-02-29T05:18:43ZengElsevierCell Reports2211-12472024-02-01432113709Decision-making dynamics are predicted by arousal and uninstructed movementsDaniel Hulsey0Kevin Zumwalt1Luca Mazzucato2David A. McCormick3Santiago Jaramillo4Institute of Neuroscience, University of Oregon, Eugene, OR 97405, USAInstitute of Neuroscience, University of Oregon, Eugene, OR 97405, USAInstitute of Neuroscience, University of Oregon, Eugene, OR 97405, USA; Department of Biology, University of Oregon, Eugene, OR 97405, USA; Departments of Physics and Mathematics, University of Oregon, Eugene, OR 97405, USA; Corresponding authorInstitute of Neuroscience, University of Oregon, Eugene, OR 97405, USA; Department of Biology, University of Oregon, Eugene, OR 97405, USA; Corresponding authorInstitute of Neuroscience, University of Oregon, Eugene, OR 97405, USA; Department of Biology, University of Oregon, Eugene, OR 97405, USA; Corresponding authorSummary: 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, using computational modeling of visual and auditory task performance data from mice, 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 find that animals fluctuate between minutes-long optimal, sub-optimal, and disengaged performance states. Optimal state epochs are predicted by intermediate levels, and reduced variability, of pupil diameter and movement. Our results demonstrate that externally observable uninstructed behaviors can predict optimal performance states and suggest that mice regulate their arousal during optimal performance.http://www.sciencedirect.com/science/article/pii/S2211124724000378CP: Neuroscience
spellingShingle Daniel Hulsey
Kevin Zumwalt
Luca Mazzucato
David A. McCormick
Santiago Jaramillo
Decision-making dynamics are predicted by arousal and uninstructed movements
Cell Reports
CP: Neuroscience
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 CP: Neuroscience
url http://www.sciencedirect.com/science/article/pii/S2211124724000378
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