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Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules
Animals face the dilemma between exploiting known opportunities and exploring new ones, a decision-making process supported by cortical circuits. While different types of learning may bias exploration, the circumstances and the degree to which bias occurs is unclear. We used an instrumental lever pr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054681/ https://www.ncbi.nlm.nih.gov/pubmed/30030509 http://dx.doi.org/10.1038/s41598-018-29285-x |
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author | Schreiner, Drew C. Gremel, Christina M. |
author_facet | Schreiner, Drew C. Gremel, Christina M. |
author_sort | Schreiner, Drew C. |
collection | PubMed |
description | Animals face the dilemma between exploiting known opportunities and exploring new ones, a decision-making process supported by cortical circuits. While different types of learning may bias exploration, the circumstances and the degree to which bias occurs is unclear. We used an instrumental lever press task in mice to examine whether learned rules generalize to exploratory situations and the cortical circuits involved. We first trained mice to press one lever for food and subsequently assessed how that learning influenced pressing of a second novel lever. Using outcome devaluation procedures we found that novel lever exploration was not dependent on the food value associated with the trained lever. Further, changes in the temporal uncertainty of when a lever press would produce food did not affect exploration. Instead, accrued experience with the instrumental contingency was strongly predictive of test lever pressing with a positive correlation between experience and trained lever exploitation, but not novel lever exploration. Chemogenetic attenuation of orbital frontal cortex (OFC) projection into secondary motor cortex (M2) biased novel lever exploration, suggesting that experience increases OFC-M2 dependent exploitation of learned associations but leaves exploration constant. Our data suggests exploitation and exploration are parallel decision-making systems that do not necessarily compete. |
format | Online Article Text |
id | pubmed-6054681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60546812018-07-23 Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules Schreiner, Drew C. Gremel, Christina M. Sci Rep Article Animals face the dilemma between exploiting known opportunities and exploring new ones, a decision-making process supported by cortical circuits. While different types of learning may bias exploration, the circumstances and the degree to which bias occurs is unclear. We used an instrumental lever press task in mice to examine whether learned rules generalize to exploratory situations and the cortical circuits involved. We first trained mice to press one lever for food and subsequently assessed how that learning influenced pressing of a second novel lever. Using outcome devaluation procedures we found that novel lever exploration was not dependent on the food value associated with the trained lever. Further, changes in the temporal uncertainty of when a lever press would produce food did not affect exploration. Instead, accrued experience with the instrumental contingency was strongly predictive of test lever pressing with a positive correlation between experience and trained lever exploitation, but not novel lever exploration. Chemogenetic attenuation of orbital frontal cortex (OFC) projection into secondary motor cortex (M2) biased novel lever exploration, suggesting that experience increases OFC-M2 dependent exploitation of learned associations but leaves exploration constant. Our data suggests exploitation and exploration are parallel decision-making systems that do not necessarily compete. Nature Publishing Group UK 2018-07-20 /pmc/articles/PMC6054681/ /pubmed/30030509 http://dx.doi.org/10.1038/s41598-018-29285-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schreiner, Drew C. Gremel, Christina M. Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules |
title | Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules |
title_full | Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules |
title_fullStr | Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules |
title_full_unstemmed | Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules |
title_short | Orbital Frontal Cortex Projections to Secondary Motor Cortex Mediate Exploitation of Learned Rules |
title_sort | orbital frontal cortex projections to secondary motor cortex mediate exploitation of learned rules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054681/ https://www.ncbi.nlm.nih.gov/pubmed/30030509 http://dx.doi.org/10.1038/s41598-018-29285-x |
work_keys_str_mv | AT schreinerdrewc orbitalfrontalcortexprojectionstosecondarymotorcortexmediateexploitationoflearnedrules AT gremelchristinam orbitalfrontalcortexprojectionstosecondarymotorcortexmediateexploitationoflearnedrules |