Cargando…

Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats

Neuronal ensembles in the infralimbic cortex (IL) develop after prolonged food self-administration training. However, rats demonstrate evidence of learning the food self-administration response as early as day 1, with responding quickly increasing to asymptotic levels. Since the contribution of indi...

Descripción completa

Detalles Bibliográficos
Autores principales: Quintana-Feliciano, Richard, Gobin, Christina, Kane, Louisa, Sortman, Bo, Rakela, Samantha, Genovese, Ariana, Tunstall, Brendan, Caprioli, Daniele, Iñiguez, Sergio D., Warren, Brandon L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174054/
https://www.ncbi.nlm.nih.gov/pubmed/33472867
http://dx.doi.org/10.1523/ENEURO.0373-20.2021
_version_ 1783702832901259264
author Quintana-Feliciano, Richard
Gobin, Christina
Kane, Louisa
Sortman, Bo
Rakela, Samantha
Genovese, Ariana
Tunstall, Brendan
Caprioli, Daniele
Iñiguez, Sergio D.
Warren, Brandon L.
author_facet Quintana-Feliciano, Richard
Gobin, Christina
Kane, Louisa
Sortman, Bo
Rakela, Samantha
Genovese, Ariana
Tunstall, Brendan
Caprioli, Daniele
Iñiguez, Sergio D.
Warren, Brandon L.
author_sort Quintana-Feliciano, Richard
collection PubMed
description Neuronal ensembles in the infralimbic cortex (IL) develop after prolonged food self-administration training. However, rats demonstrate evidence of learning the food self-administration response as early as day 1, with responding quickly increasing to asymptotic levels. Since the contribution of individual brain regions to task performance shifts over the course of training, it remains unclear whether IL ensembles are gradually formed and refined over the course of extensive operant training, or whether functionally-relevant ensembles might be recruited and formed as early as the initial acquisition of food self-administration behavior. Here, we aimed to determine the role of IL ensembles at the earliest possible point after demonstrable learning of a response-outcome association. We first allowed rats to lever press for palatable food pellets and stopped training rats once their behavior evidenced the response-outcome association (learners). We compared their food-seeking behavior and neuronal activation (Fos protein expression) to similarly trained rats that did not form this association (non-learners). Learners had greater food-seeking behavior and neuronal activation within the medial prefrontal cortex (mPFC), suggesting that mPFC subregions might encode initial food self-administration memories. To test the functional relevance of mPFC Fos-expressing ensembles to subsequent food seeking, we tested region-wide inactivation of the IL using muscimol+baclofen and neuronal ensemble-specific ablation using the Daun02 inactivation procedure. Both region-wide inactivation and ensemble-specific inactivation of the IL significantly decreased food seeking. These data suggest that IL neuronal ensembles form during initial learning of food self-administration behavior, and furthermore, that these ensembles play a functional role in food seeking.
format Online
Article
Text
id pubmed-8174054
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-81740542021-06-03 Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats Quintana-Feliciano, Richard Gobin, Christina Kane, Louisa Sortman, Bo Rakela, Samantha Genovese, Ariana Tunstall, Brendan Caprioli, Daniele Iñiguez, Sergio D. Warren, Brandon L. eNeuro Research Article: New Research Neuronal ensembles in the infralimbic cortex (IL) develop after prolonged food self-administration training. However, rats demonstrate evidence of learning the food self-administration response as early as day 1, with responding quickly increasing to asymptotic levels. Since the contribution of individual brain regions to task performance shifts over the course of training, it remains unclear whether IL ensembles are gradually formed and refined over the course of extensive operant training, or whether functionally-relevant ensembles might be recruited and formed as early as the initial acquisition of food self-administration behavior. Here, we aimed to determine the role of IL ensembles at the earliest possible point after demonstrable learning of a response-outcome association. We first allowed rats to lever press for palatable food pellets and stopped training rats once their behavior evidenced the response-outcome association (learners). We compared their food-seeking behavior and neuronal activation (Fos protein expression) to similarly trained rats that did not form this association (non-learners). Learners had greater food-seeking behavior and neuronal activation within the medial prefrontal cortex (mPFC), suggesting that mPFC subregions might encode initial food self-administration memories. To test the functional relevance of mPFC Fos-expressing ensembles to subsequent food seeking, we tested region-wide inactivation of the IL using muscimol+baclofen and neuronal ensemble-specific ablation using the Daun02 inactivation procedure. Both region-wide inactivation and ensemble-specific inactivation of the IL significantly decreased food seeking. These data suggest that IL neuronal ensembles form during initial learning of food self-administration behavior, and furthermore, that these ensembles play a functional role in food seeking. Society for Neuroscience 2021-04-05 /pmc/articles/PMC8174054/ /pubmed/33472867 http://dx.doi.org/10.1523/ENEURO.0373-20.2021 Text en Copyright © 2021 Quintana-Feliciano et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Quintana-Feliciano, Richard
Gobin, Christina
Kane, Louisa
Sortman, Bo
Rakela, Samantha
Genovese, Ariana
Tunstall, Brendan
Caprioli, Daniele
Iñiguez, Sergio D.
Warren, Brandon L.
Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats
title Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats
title_full Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats
title_fullStr Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats
title_full_unstemmed Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats
title_short Food-Seeking Behavior Is Mediated by Fos-Expressing Neuronal Ensembles Formed at First Learning in Rats
title_sort food-seeking behavior is mediated by fos-expressing neuronal ensembles formed at first learning in rats
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174054/
https://www.ncbi.nlm.nih.gov/pubmed/33472867
http://dx.doi.org/10.1523/ENEURO.0373-20.2021
work_keys_str_mv AT quintanafelicianorichard foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT gobinchristina foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT kanelouisa foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT sortmanbo foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT rakelasamantha foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT genoveseariana foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT tunstallbrendan foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT capriolidaniele foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT iniguezsergiod foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats
AT warrenbrandonl foodseekingbehaviorismediatedbyfosexpressingneuronalensemblesformedatfirstlearninginrats