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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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. |
format | Online Article Text |
id | pubmed-10196573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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