Cortical and subcortical activities during food rewards versus social interaction in rats
Abstract Balancing food foraging with social interaction is crucial for survival and reproduction in many species of mammals. We wanted to investigate the reward preferences in adult male rats by allowing them to lever-press for both food and social rewards (interaction with another rat), while thei...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2025-02-01
|
Series: | Scientific Reports |
Subjects: | |
Online Access: | https://doi.org/10.1038/s41598-025-87880-1 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1823862499296935936 |
---|---|
author | Florbela Rocha-Almeida Ana R. Conde-Moro Antonio Fernández-Ruiz José M. Delgado-García Agnès Gruart |
author_facet | Florbela Rocha-Almeida Ana R. Conde-Moro Antonio Fernández-Ruiz José M. Delgado-García Agnès Gruart |
author_sort | Florbela Rocha-Almeida |
collection | DOAJ |
description | Abstract Balancing food foraging with social interaction is crucial for survival and reproduction in many species of mammals. We wanted to investigate the reward preferences in adult male rats by allowing them to lever-press for both food and social rewards (interaction with another rat), while their performance and electrophysiological activities were recorded. Local field potentials (LFPs) were analyzed across five neuroanatomical regions involved in reward processing, decision-making, and social behavior. Despite ad libitum food availability, rats consistently prioritized food. LFP analysis revealed a decrease in nucleus accumbens (NAc) spectral power following social interaction, accompanied by specific alterations in delta and theta bands within the medial prefrontal cortex (mPFC). The spectral power of LFPs delta and/or theta bands were different for the five selected regions following food reward vs. social interactions. Cross-frequency coupling analysis provided further insights, demonstrating dynamic changes in theta-to-gamma coupling during both food and social rewards, with distinct roles for slow- and fast-gamma frequencies. These findings shed light on the intricate neural processes underlying reward preferences and/or decision-making choices, highlighting the NAc’s potential role in social reward processing, and the mPFC’s involvement in modulating theta–gamma rhythms during reward-related decision-making. |
format | Article |
id | doaj-art-95c49f9c540f479d874f61caefb8dbb3 |
institution | Kabale University |
issn | 2045-2322 |
language | English |
publishDate | 2025-02-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Scientific Reports |
spelling | doaj-art-95c49f9c540f479d874f61caefb8dbb32025-02-09T12:30:00ZengNature PortfolioScientific Reports2045-23222025-02-0115111310.1038/s41598-025-87880-1Cortical and subcortical activities during food rewards versus social interaction in ratsFlorbela Rocha-Almeida0Ana R. Conde-Moro1Antonio Fernández-Ruiz2José M. Delgado-García3Agnès Gruart4Division of Neurosciences, Pablo de Olavide UniversityDivision of Neurosciences, Pablo de Olavide UniversityDepartment of Neurobiology and Behavior, Cornell UniversityDivision of Neurosciences, Pablo de Olavide UniversityDivision of Neurosciences, Pablo de Olavide UniversityAbstract Balancing food foraging with social interaction is crucial for survival and reproduction in many species of mammals. We wanted to investigate the reward preferences in adult male rats by allowing them to lever-press for both food and social rewards (interaction with another rat), while their performance and electrophysiological activities were recorded. Local field potentials (LFPs) were analyzed across five neuroanatomical regions involved in reward processing, decision-making, and social behavior. Despite ad libitum food availability, rats consistently prioritized food. LFP analysis revealed a decrease in nucleus accumbens (NAc) spectral power following social interaction, accompanied by specific alterations in delta and theta bands within the medial prefrontal cortex (mPFC). The spectral power of LFPs delta and/or theta bands were different for the five selected regions following food reward vs. social interactions. Cross-frequency coupling analysis provided further insights, demonstrating dynamic changes in theta-to-gamma coupling during both food and social rewards, with distinct roles for slow- and fast-gamma frequencies. These findings shed light on the intricate neural processes underlying reward preferences and/or decision-making choices, highlighting the NAc’s potential role in social reward processing, and the mPFC’s involvement in modulating theta–gamma rhythms during reward-related decision-making.https://doi.org/10.1038/s41598-025-87880-1RatsReward preferenceFoodSocial interactionElectrophysiologyTheta–Gamma coupling |
spellingShingle | Florbela Rocha-Almeida Ana R. Conde-Moro Antonio Fernández-Ruiz José M. Delgado-García Agnès Gruart Cortical and subcortical activities during food rewards versus social interaction in rats Scientific Reports Rats Reward preference Food Social interaction Electrophysiology Theta–Gamma coupling |
title | Cortical and subcortical activities during food rewards versus social interaction in rats |
title_full | Cortical and subcortical activities during food rewards versus social interaction in rats |
title_fullStr | Cortical and subcortical activities during food rewards versus social interaction in rats |
title_full_unstemmed | Cortical and subcortical activities during food rewards versus social interaction in rats |
title_short | Cortical and subcortical activities during food rewards versus social interaction in rats |
title_sort | cortical and subcortical activities during food rewards versus social interaction in rats |
topic | Rats Reward preference Food Social interaction Electrophysiology Theta–Gamma coupling |
url | https://doi.org/10.1038/s41598-025-87880-1 |
work_keys_str_mv | AT florbelarochaalmeida corticalandsubcorticalactivitiesduringfoodrewardsversussocialinteractioninrats AT anarcondemoro corticalandsubcorticalactivitiesduringfoodrewardsversussocialinteractioninrats AT antoniofernandezruiz corticalandsubcorticalactivitiesduringfoodrewardsversussocialinteractioninrats AT josemdelgadogarcia corticalandsubcorticalactivitiesduringfoodrewardsversussocialinteractioninrats AT agnesgruart corticalandsubcorticalactivitiesduringfoodrewardsversussocialinteractioninrats |