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The role of mPFC and MTL neurons in human choice under goal-conflict

Resolving approach-avoidance conflicts relies on encoding motivation outcomes and learning from past experiences. Accumulating evidence points to the role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these processes, but their differential contributions have not been conv...

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Autores principales: Gazit, Tomer, Gonen, Tal, Gurevitch, Guy, Cohen, Noa, Strauss, Ido, Zeevi, Yoav, Yamin, Hagar, Fahoum, Firas, Hendler, Talma, Fried, Itzhak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314808/
https://www.ncbi.nlm.nih.gov/pubmed/32581214
http://dx.doi.org/10.1038/s41467-020-16908-z
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author Gazit, Tomer
Gonen, Tal
Gurevitch, Guy
Cohen, Noa
Strauss, Ido
Zeevi, Yoav
Yamin, Hagar
Fahoum, Firas
Hendler, Talma
Fried, Itzhak
author_facet Gazit, Tomer
Gonen, Tal
Gurevitch, Guy
Cohen, Noa
Strauss, Ido
Zeevi, Yoav
Yamin, Hagar
Fahoum, Firas
Hendler, Talma
Fried, Itzhak
author_sort Gazit, Tomer
collection PubMed
description Resolving approach-avoidance conflicts relies on encoding motivation outcomes and learning from past experiences. Accumulating evidence points to the role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these processes, but their differential contributions have not been convincingly deciphered in humans. We detect 310 neurons from mPFC and MTL from patients with epilepsy undergoing intracranial recordings and participating in a goal-conflict task where rewards and punishments could be controlled or not. mPFC neurons are more selective to punishments than rewards when controlled. However, only MTL firing following punishment is linked to a lower probability for subsequent approach behavior. mPFC response to punishment precedes a similar MTL response and affects subsequent behavior via an interaction with MTL firing. We thus propose a model where approach-avoidance conflict resolution in humans depends on outcome value tagging in mPFC neurons influencing encoding of such value in MTL to affect subsequent choice.
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spelling pubmed-73148082020-06-26 The role of mPFC and MTL neurons in human choice under goal-conflict Gazit, Tomer Gonen, Tal Gurevitch, Guy Cohen, Noa Strauss, Ido Zeevi, Yoav Yamin, Hagar Fahoum, Firas Hendler, Talma Fried, Itzhak Nat Commun Article Resolving approach-avoidance conflicts relies on encoding motivation outcomes and learning from past experiences. Accumulating evidence points to the role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these processes, but their differential contributions have not been convincingly deciphered in humans. We detect 310 neurons from mPFC and MTL from patients with epilepsy undergoing intracranial recordings and participating in a goal-conflict task where rewards and punishments could be controlled or not. mPFC neurons are more selective to punishments than rewards when controlled. However, only MTL firing following punishment is linked to a lower probability for subsequent approach behavior. mPFC response to punishment precedes a similar MTL response and affects subsequent behavior via an interaction with MTL firing. We thus propose a model where approach-avoidance conflict resolution in humans depends on outcome value tagging in mPFC neurons influencing encoding of such value in MTL to affect subsequent choice. Nature Publishing Group UK 2020-06-24 /pmc/articles/PMC7314808/ /pubmed/32581214 http://dx.doi.org/10.1038/s41467-020-16908-z Text en © The Author(s) 2020 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
Gazit, Tomer
Gonen, Tal
Gurevitch, Guy
Cohen, Noa
Strauss, Ido
Zeevi, Yoav
Yamin, Hagar
Fahoum, Firas
Hendler, Talma
Fried, Itzhak
The role of mPFC and MTL neurons in human choice under goal-conflict
title The role of mPFC and MTL neurons in human choice under goal-conflict
title_full The role of mPFC and MTL neurons in human choice under goal-conflict
title_fullStr The role of mPFC and MTL neurons in human choice under goal-conflict
title_full_unstemmed The role of mPFC and MTL neurons in human choice under goal-conflict
title_short The role of mPFC and MTL neurons in human choice under goal-conflict
title_sort role of mpfc and mtl neurons in human choice under goal-conflict
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314808/
https://www.ncbi.nlm.nih.gov/pubmed/32581214
http://dx.doi.org/10.1038/s41467-020-16908-z
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