Selection and inhibition mechanisms for human voluntary action decisions

One can choose between action alternatives that have no apparent difference in their outcomes. Such voluntary action decisions are associated with widespread frontal–parietal activation, and a tendency to inhibit the repetition of a previous action. However, the mechanism of initiating voluntary act...

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Main Authors: Zhang, Jiaxiang, Hughes, Laura E., Rowe, James B.
Format: Online
Language:English
Published: Academic Press 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445813/
id pubmed-3445813
recordtype oai_dc
spelling pubmed-34458132012-10-15 Selection and inhibition mechanisms for human voluntary action decisions Zhang, Jiaxiang Hughes, Laura E. Rowe, James B. Article One can choose between action alternatives that have no apparent difference in their outcomes. Such voluntary action decisions are associated with widespread frontal–parietal activation, and a tendency to inhibit the repetition of a previous action. However, the mechanism of initiating voluntary actions and the functions of different brain regions during this process remains largely unknown. Here, we combine computational modeling and functional magnetic resonance imaging to test the selection and inhibition mechanisms that mediate trial-to-trial voluntary action decisions. We fitted an optimized accumulator model to behavioral responses in a finger-tapping task in which participants were instructed to make chosen actions or specified actions. Model parameters derived from each individual were then applied to estimate the expected accumulated metabolic activity (EAA) engaged in every single trial. The EAA was associated with blood oxygenation level-dependent responses in a decision work that was maximal in the supplementary motor area and the caudal anterior cingulate cortex, consistent with a competitive accumulation-to-threshold mechanism for action decision by these regions. Furthermore, specific inhibition of the previous action's accumulator was related to the suppression of response repetition. This action-specific inhibition correlated with the activity of the right inferior frontal gyrus, when the option to repeat existed. Our findings suggest that human voluntary action decisions are mediated by complementary processes of intentional selection and inhibition. Academic Press 2012-10-15 /pmc/articles/PMC3445813/ /pubmed/22776456 http://dx.doi.org/10.1016/j.neuroimage.2012.06.058 Text en © 2012 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Zhang, Jiaxiang
Hughes, Laura E.
Rowe, James B.
spellingShingle Zhang, Jiaxiang
Hughes, Laura E.
Rowe, James B.
Selection and inhibition mechanisms for human voluntary action decisions
author_facet Zhang, Jiaxiang
Hughes, Laura E.
Rowe, James B.
author_sort Zhang, Jiaxiang
title Selection and inhibition mechanisms for human voluntary action decisions
title_short Selection and inhibition mechanisms for human voluntary action decisions
title_full Selection and inhibition mechanisms for human voluntary action decisions
title_fullStr Selection and inhibition mechanisms for human voluntary action decisions
title_full_unstemmed Selection and inhibition mechanisms for human voluntary action decisions
title_sort selection and inhibition mechanisms for human voluntary action decisions
description One can choose between action alternatives that have no apparent difference in their outcomes. Such voluntary action decisions are associated with widespread frontal–parietal activation, and a tendency to inhibit the repetition of a previous action. However, the mechanism of initiating voluntary actions and the functions of different brain regions during this process remains largely unknown. Here, we combine computational modeling and functional magnetic resonance imaging to test the selection and inhibition mechanisms that mediate trial-to-trial voluntary action decisions. We fitted an optimized accumulator model to behavioral responses in a finger-tapping task in which participants were instructed to make chosen actions or specified actions. Model parameters derived from each individual were then applied to estimate the expected accumulated metabolic activity (EAA) engaged in every single trial. The EAA was associated with blood oxygenation level-dependent responses in a decision work that was maximal in the supplementary motor area and the caudal anterior cingulate cortex, consistent with a competitive accumulation-to-threshold mechanism for action decision by these regions. Furthermore, specific inhibition of the previous action's accumulator was related to the suppression of response repetition. This action-specific inhibition correlated with the activity of the right inferior frontal gyrus, when the option to repeat existed. Our findings suggest that human voluntary action decisions are mediated by complementary processes of intentional selection and inhibition.
publisher Academic Press
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445813/
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