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Decision-making dynamics are predicted by arousal and uninstructed movements.
Hulsey, Daniel; Zumwalt, Kevin; Mazzucato, Luca; McCormick, David A; Jaramillo, Santiago.
Affiliation
  • Hulsey D; Institute of Neuroscience, University of Oregon, Eugene, OR 97405, USA.
  • Zumwalt K; Institute of Neuroscience, University of Oregon, Eugene, OR 97405, USA.
  • Mazzucato L; Institute 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. Electronic address: lmazzuca@uoregon.edu.
  • McCormick DA; Institute of Neuroscience, University of Oregon, Eugene, OR 97405, USA; Department of Biology, University of Oregon, Eugene, OR 97405, USA. Electronic address: davidmc@uoregon.edu.
  • Jaramillo S; Institute of Neuroscience, University of Oregon, Eugene, OR 97405, USA; Department of Biology, University of Oregon, Eugene, OR 97405, USA. Electronic address: sjara@uoregon.edu.
Cell Rep ; 43(2): 113709, 2024 Feb 27.
Article in En | MEDLINE | ID: mdl-38280196
ABSTRACT
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arousal / Movement Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: Cell Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arousal / Movement Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: Cell Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States