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Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations

The ability to respond flexibly to an ever-changing environment relies on the orbitofrontal cortex (OFC). However, how the OFC associates sensory information with predicted outcomes to enable flexible sensory learning in humans remains elusive. Here, we combine a probabilistic tactile reversal learn...

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Autores principales: Wang, Bin A., Veismann, Maike, Banerjee, Abhishek, Pleger, Burkhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272188/
https://www.ncbi.nlm.nih.gov/pubmed/37322004
http://dx.doi.org/10.1038/s41467-023-38671-7
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author Wang, Bin A.
Veismann, Maike
Banerjee, Abhishek
Pleger, Burkhard
author_facet Wang, Bin A.
Veismann, Maike
Banerjee, Abhishek
Pleger, Burkhard
author_sort Wang, Bin A.
collection PubMed
description The ability to respond flexibly to an ever-changing environment relies on the orbitofrontal cortex (OFC). However, how the OFC associates sensory information with predicted outcomes to enable flexible sensory learning in humans remains elusive. Here, we combine a probabilistic tactile reversal learning task with functional magnetic resonance imaging (fMRI) to investigate how lateral OFC (lOFC) interacts with the primary somatosensory cortex (S1) to guide flexible tactile learning in humans. fMRI results reveal that lOFC and S1 exhibit distinct task-dependent engagement: while the lOFC responds transiently to unexpected outcomes immediately following reversals, S1 is persistently engaged during re-learning. Unlike the contralateral stimulus-selective S1, activity in ipsilateral S1 mirrors the outcomes of behavior during re-learning, closely related to top-down signals from lOFC. These findings suggest that lOFC contributes to teaching signals to dynamically update representations in sensory areas, which implement computations critical for adaptive behavior.
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spelling pubmed-102721882023-06-17 Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations Wang, Bin A. Veismann, Maike Banerjee, Abhishek Pleger, Burkhard Nat Commun Article The ability to respond flexibly to an ever-changing environment relies on the orbitofrontal cortex (OFC). However, how the OFC associates sensory information with predicted outcomes to enable flexible sensory learning in humans remains elusive. Here, we combine a probabilistic tactile reversal learning task with functional magnetic resonance imaging (fMRI) to investigate how lateral OFC (lOFC) interacts with the primary somatosensory cortex (S1) to guide flexible tactile learning in humans. fMRI results reveal that lOFC and S1 exhibit distinct task-dependent engagement: while the lOFC responds transiently to unexpected outcomes immediately following reversals, S1 is persistently engaged during re-learning. Unlike the contralateral stimulus-selective S1, activity in ipsilateral S1 mirrors the outcomes of behavior during re-learning, closely related to top-down signals from lOFC. These findings suggest that lOFC contributes to teaching signals to dynamically update representations in sensory areas, which implement computations critical for adaptive behavior. Nature Publishing Group UK 2023-06-15 /pmc/articles/PMC10272188/ /pubmed/37322004 http://dx.doi.org/10.1038/s41467-023-38671-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Bin A.
Veismann, Maike
Banerjee, Abhishek
Pleger, Burkhard
Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations
title Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations
title_full Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations
title_fullStr Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations
title_full_unstemmed Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations
title_short Human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations
title_sort human orbitofrontal cortex signals decision outcomes to sensory cortex during behavioral adaptations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272188/
https://www.ncbi.nlm.nih.gov/pubmed/37322004
http://dx.doi.org/10.1038/s41467-023-38671-7
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