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Pupil size predicts the onset of exploration in brain and behavior
In uncertain environments, intelligent decision-makers exploit actions that have been rewarding in the past, but also explore actions that could be even better. Several neuromodulatory systems are implicated in exploration, based, in part, on work linking exploration to pupil size–a peripheral corre...
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/PMC10245915/ https://www.ncbi.nlm.nih.gov/pubmed/37292773 http://dx.doi.org/10.1101/2023.05.24.541981 |
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author | Shourkeshti, Akram Marrocco, Gabriel Jurewicz, Katarzyna Moore, Tirin Ebitz, R. Becket |
author_facet | Shourkeshti, Akram Marrocco, Gabriel Jurewicz, Katarzyna Moore, Tirin Ebitz, R. Becket |
author_sort | Shourkeshti, Akram |
collection | PubMed |
description | In uncertain environments, intelligent decision-makers exploit actions that have been rewarding in the past, but also explore actions that could be even better. Several neuromodulatory systems are implicated in exploration, based, in part, on work linking exploration to pupil size–a peripheral correlate of neuromodulatory tone and index of arousal. However, pupil size could instead track variables that make exploration more likely, like volatility or reward, without directly predicting either exploration or its neural bases. Here, we simultaneously measured pupil size, exploration, and neural population activity in the prefrontal cortex while two rhesus macaques explored and exploited in a dynamic environment. We found that pupil size under constant luminance specifically predicted the onset of exploration, beyond what could be explained by reward history. Pupil size also predicted disorganized patterns of prefrontal neural activity at both the single neuron and population levels, even within periods of exploitation. Ultimately, our results support a model in which pupil-linked mechanisms promote the onset of exploration via driving the prefrontal cortex through a critical tipping point where prefrontal control dynamics become disorganized and exploratory decisions are possible. |
format | Online Article Text |
id | pubmed-10245915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-102459152023-06-08 Pupil size predicts the onset of exploration in brain and behavior Shourkeshti, Akram Marrocco, Gabriel Jurewicz, Katarzyna Moore, Tirin Ebitz, R. Becket bioRxiv Article In uncertain environments, intelligent decision-makers exploit actions that have been rewarding in the past, but also explore actions that could be even better. Several neuromodulatory systems are implicated in exploration, based, in part, on work linking exploration to pupil size–a peripheral correlate of neuromodulatory tone and index of arousal. However, pupil size could instead track variables that make exploration more likely, like volatility or reward, without directly predicting either exploration or its neural bases. Here, we simultaneously measured pupil size, exploration, and neural population activity in the prefrontal cortex while two rhesus macaques explored and exploited in a dynamic environment. We found that pupil size under constant luminance specifically predicted the onset of exploration, beyond what could be explained by reward history. Pupil size also predicted disorganized patterns of prefrontal neural activity at both the single neuron and population levels, even within periods of exploitation. Ultimately, our results support a model in which pupil-linked mechanisms promote the onset of exploration via driving the prefrontal cortex through a critical tipping point where prefrontal control dynamics become disorganized and exploratory decisions are possible. Cold Spring Harbor Laboratory 2023-05-24 /pmc/articles/PMC10245915/ /pubmed/37292773 http://dx.doi.org/10.1101/2023.05.24.541981 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 Shourkeshti, Akram Marrocco, Gabriel Jurewicz, Katarzyna Moore, Tirin Ebitz, R. Becket Pupil size predicts the onset of exploration in brain and behavior |
title | Pupil size predicts the onset of exploration in brain and behavior |
title_full | Pupil size predicts the onset of exploration in brain and behavior |
title_fullStr | Pupil size predicts the onset of exploration in brain and behavior |
title_full_unstemmed | Pupil size predicts the onset of exploration in brain and behavior |
title_short | Pupil size predicts the onset of exploration in brain and behavior |
title_sort | pupil size predicts the onset of exploration in brain and behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245915/ https://www.ncbi.nlm.nih.gov/pubmed/37292773 http://dx.doi.org/10.1101/2023.05.24.541981 |
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