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Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules

Foraging in animals relies on innate decision-making heuristics that can result in suboptimal cognitive biases in some contexts. The mechanisms underlying these biases are not well understood, but likely involve strong genetic effects. To explore this, we studied fasted mice using a naturalistic for...

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Autores principales: Ravens, Alicia, Stacher-Hörndli, Cornelia N., Emery, Jared, Steinwand, Susan, Shepherd, Jason D., Gregg, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196573/
https://www.ncbi.nlm.nih.gov/pubmed/37216088
http://dx.doi.org/10.1016/j.isci.2023.106761
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author Ravens, Alicia
Stacher-Hörndli, Cornelia N.
Emery, Jared
Steinwand, Susan
Shepherd, Jason D.
Gregg, Christopher
author_facet Ravens, Alicia
Stacher-Hörndli, Cornelia N.
Emery, Jared
Steinwand, Susan
Shepherd, Jason D.
Gregg, Christopher
author_sort Ravens, Alicia
collection PubMed
description Foraging in animals relies on innate decision-making heuristics that can result in suboptimal cognitive biases in some contexts. The mechanisms underlying these biases are not well understood, but likely involve strong genetic effects. To explore this, we studied fasted mice using a naturalistic foraging paradigm and discovered an innate cognitive bias called “second-guessing.” This involves repeatedly investigating an empty former food patch instead of consuming available food, which hinders the mice from maximizing feeding benefits. The synaptic plasticity gene Arc is revealed to play a role in this bias, as Arc-deficient mice did not exhibit second-guessing and consumed more food. In addition, unsupervised machine learning decompositions of foraging identified specific behavior sequences, or “modules”, that are affected by Arc. These findings highlight the genetic basis of cognitive biases in decision making, show links between behavior modules and cognitive bias, and provide insight into the ethological roles of Arc in naturalistic foraging.
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spelling pubmed-101965732023-05-20 Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules Ravens, Alicia Stacher-Hörndli, Cornelia N. Emery, Jared Steinwand, Susan Shepherd, Jason D. Gregg, Christopher iScience Article Foraging in animals relies on innate decision-making heuristics that can result in suboptimal cognitive biases in some contexts. The mechanisms underlying these biases are not well understood, but likely involve strong genetic effects. To explore this, we studied fasted mice using a naturalistic foraging paradigm and discovered an innate cognitive bias called “second-guessing.” This involves repeatedly investigating an empty former food patch instead of consuming available food, which hinders the mice from maximizing feeding benefits. The synaptic plasticity gene Arc is revealed to play a role in this bias, as Arc-deficient mice did not exhibit second-guessing and consumed more food. In addition, unsupervised machine learning decompositions of foraging identified specific behavior sequences, or “modules”, that are affected by Arc. These findings highlight the genetic basis of cognitive biases in decision making, show links between behavior modules and cognitive bias, and provide insight into the ethological roles of Arc in naturalistic foraging. Elsevier 2023-04-27 /pmc/articles/PMC10196573/ /pubmed/37216088 http://dx.doi.org/10.1016/j.isci.2023.106761 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ravens, Alicia
Stacher-Hörndli, Cornelia N.
Emery, Jared
Steinwand, Susan
Shepherd, Jason D.
Gregg, Christopher
Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules
title Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules
title_full Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules
title_fullStr Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules
title_full_unstemmed Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules
title_short Arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules
title_sort arc regulates a second-guessing cognitive bias during naturalistic foraging through effects on discrete behavior modules
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196573/
https://www.ncbi.nlm.nih.gov/pubmed/37216088
http://dx.doi.org/10.1016/j.isci.2023.106761
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