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Striatal BOLD and midfrontal theta power express motivation for action

Action selection is biased by the valence of anticipated outcomes. To assess mechanisms by which these motivational biases are expressed and controlled, we measured simultaneous EEG-fMRI during a motivational Go/NoGo learning task (N = 36), leveraging the temporal resolution of EEG and subcortical a...

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Autores principales: Algermissen, Johannes, Swart, Jennifer C, Scheeringa, René, Cools, Roshan, den Ouden, Hanneke E M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290551/
https://www.ncbi.nlm.nih.gov/pubmed/34849626
http://dx.doi.org/10.1093/cercor/bhab391
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author Algermissen, Johannes
Swart, Jennifer C
Scheeringa, René
Cools, Roshan
den Ouden, Hanneke E M
author_facet Algermissen, Johannes
Swart, Jennifer C
Scheeringa, René
Cools, Roshan
den Ouden, Hanneke E M
author_sort Algermissen, Johannes
collection PubMed
description Action selection is biased by the valence of anticipated outcomes. To assess mechanisms by which these motivational biases are expressed and controlled, we measured simultaneous EEG-fMRI during a motivational Go/NoGo learning task (N = 36), leveraging the temporal resolution of EEG and subcortical access of fMRI. VmPFC BOLD encoded cue valence, importantly predicting trial-by-trial valence-driven response speed differences and EEG theta power around cue onset. In contrast, striatal BOLD encoded selection of active Go responses and correlated with theta power around response time. Within trials, theta power ramped in the fashion of an evidence accumulation signal for the value of making a “Go” response, capturing the faster responding to reward cues. Our findings reveal a dual nature of midfrontal theta power, with early components reflecting the vmPFC contribution to motivational biases, and late components reflecting their striatal translation into behavior, in line with influential recent “value of work” theories of striatal processing.
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spelling pubmed-92905512022-07-18 Striatal BOLD and midfrontal theta power express motivation for action Algermissen, Johannes Swart, Jennifer C Scheeringa, René Cools, Roshan den Ouden, Hanneke E M Cereb Cortex Original Article Action selection is biased by the valence of anticipated outcomes. To assess mechanisms by which these motivational biases are expressed and controlled, we measured simultaneous EEG-fMRI during a motivational Go/NoGo learning task (N = 36), leveraging the temporal resolution of EEG and subcortical access of fMRI. VmPFC BOLD encoded cue valence, importantly predicting trial-by-trial valence-driven response speed differences and EEG theta power around cue onset. In contrast, striatal BOLD encoded selection of active Go responses and correlated with theta power around response time. Within trials, theta power ramped in the fashion of an evidence accumulation signal for the value of making a “Go” response, capturing the faster responding to reward cues. Our findings reveal a dual nature of midfrontal theta power, with early components reflecting the vmPFC contribution to motivational biases, and late components reflecting their striatal translation into behavior, in line with influential recent “value of work” theories of striatal processing. Oxford University Press 2021-11-24 /pmc/articles/PMC9290551/ /pubmed/34849626 http://dx.doi.org/10.1093/cercor/bhab391 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Algermissen, Johannes
Swart, Jennifer C
Scheeringa, René
Cools, Roshan
den Ouden, Hanneke E M
Striatal BOLD and midfrontal theta power express motivation for action
title Striatal BOLD and midfrontal theta power express motivation for action
title_full Striatal BOLD and midfrontal theta power express motivation for action
title_fullStr Striatal BOLD and midfrontal theta power express motivation for action
title_full_unstemmed Striatal BOLD and midfrontal theta power express motivation for action
title_short Striatal BOLD and midfrontal theta power express motivation for action
title_sort striatal bold and midfrontal theta power express motivation for action
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290551/
https://www.ncbi.nlm.nih.gov/pubmed/34849626
http://dx.doi.org/10.1093/cercor/bhab391
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