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Quantifying the Reconfiguration of Intrinsic Networks during Working Memory

Rapid, flexible reconfiguration of connections across brain regions is thought to underlie successful cognitive control. Two intrinsic networks in particular, the cingulo-opercular (CO) and fronto-parietal (FP), are thought to underlie two operations critical for cognitive control: task-set maintena...

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Detalles Bibliográficos
Autores principales: Cohen, Jessica R., Gallen, Courtney L., Jacobs, Emily G., Lee, Taraz G., D'Esposito, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156328/
https://www.ncbi.nlm.nih.gov/pubmed/25191704
http://dx.doi.org/10.1371/journal.pone.0106636
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author Cohen, Jessica R.
Gallen, Courtney L.
Jacobs, Emily G.
Lee, Taraz G.
D'Esposito, Mark
author_facet Cohen, Jessica R.
Gallen, Courtney L.
Jacobs, Emily G.
Lee, Taraz G.
D'Esposito, Mark
author_sort Cohen, Jessica R.
collection PubMed
description Rapid, flexible reconfiguration of connections across brain regions is thought to underlie successful cognitive control. Two intrinsic networks in particular, the cingulo-opercular (CO) and fronto-parietal (FP), are thought to underlie two operations critical for cognitive control: task-set maintenance/tonic alertness and adaptive, trial-by-trial updating. Using functional magnetic resonance imaging, we directly tested whether the functional connectivity of the CO and FP networks was related to cognitive demands and behavior. We focused on working memory because of evidence that during working memory tasks the entire brain becomes more integrated. When specifically probing the CO and FP cognitive control networks, we found that individual regions of both intrinsic networks were active during working memory and, as expected, integration across the two networks increased during task blocks that required cognitive control. Crucially, increased integration between each of the cognitive control networks and a task-related, non-cognitive control network (the hand somatosensory-motor network; SM) was related to increased accuracy. This implies that dynamic reconfiguration of the CO and FP networks so as to increase their inter-network communication underlies successful working memory.
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spelling pubmed-41563282014-09-09 Quantifying the Reconfiguration of Intrinsic Networks during Working Memory Cohen, Jessica R. Gallen, Courtney L. Jacobs, Emily G. Lee, Taraz G. D'Esposito, Mark PLoS One Research Article Rapid, flexible reconfiguration of connections across brain regions is thought to underlie successful cognitive control. Two intrinsic networks in particular, the cingulo-opercular (CO) and fronto-parietal (FP), are thought to underlie two operations critical for cognitive control: task-set maintenance/tonic alertness and adaptive, trial-by-trial updating. Using functional magnetic resonance imaging, we directly tested whether the functional connectivity of the CO and FP networks was related to cognitive demands and behavior. We focused on working memory because of evidence that during working memory tasks the entire brain becomes more integrated. When specifically probing the CO and FP cognitive control networks, we found that individual regions of both intrinsic networks were active during working memory and, as expected, integration across the two networks increased during task blocks that required cognitive control. Crucially, increased integration between each of the cognitive control networks and a task-related, non-cognitive control network (the hand somatosensory-motor network; SM) was related to increased accuracy. This implies that dynamic reconfiguration of the CO and FP networks so as to increase their inter-network communication underlies successful working memory. Public Library of Science 2014-09-05 /pmc/articles/PMC4156328/ /pubmed/25191704 http://dx.doi.org/10.1371/journal.pone.0106636 Text en © 2014 Cohen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cohen, Jessica R.
Gallen, Courtney L.
Jacobs, Emily G.
Lee, Taraz G.
D'Esposito, Mark
Quantifying the Reconfiguration of Intrinsic Networks during Working Memory
title Quantifying the Reconfiguration of Intrinsic Networks during Working Memory
title_full Quantifying the Reconfiguration of Intrinsic Networks during Working Memory
title_fullStr Quantifying the Reconfiguration of Intrinsic Networks during Working Memory
title_full_unstemmed Quantifying the Reconfiguration of Intrinsic Networks during Working Memory
title_short Quantifying the Reconfiguration of Intrinsic Networks during Working Memory
title_sort quantifying the reconfiguration of intrinsic networks during working memory
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156328/
https://www.ncbi.nlm.nih.gov/pubmed/25191704
http://dx.doi.org/10.1371/journal.pone.0106636
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