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Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network

How does the human brain rapidly process incoming information in working memory? In growing divergence from a single-region focus on the prefrontal cortex (PFC), recent work argues for emphasis on how distributed neural networks are rapidly coordinated in support of this central neurocognitive funct...

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Autores principales: Johnson, Elizabeth L., King-Stephens, David, Weber, Peter B., Laxer, Kenneth D., Lin, Jack J., Knight, Robert T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333050/
https://www.ncbi.nlm.nih.gov/pubmed/30670953
http://dx.doi.org/10.3389/fnsys.2018.00065
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author Johnson, Elizabeth L.
King-Stephens, David
Weber, Peter B.
Laxer, Kenneth D.
Lin, Jack J.
Knight, Robert T.
author_facet Johnson, Elizabeth L.
King-Stephens, David
Weber, Peter B.
Laxer, Kenneth D.
Lin, Jack J.
Knight, Robert T.
author_sort Johnson, Elizabeth L.
collection PubMed
description How does the human brain rapidly process incoming information in working memory? In growing divergence from a single-region focus on the prefrontal cortex (PFC), recent work argues for emphasis on how distributed neural networks are rapidly coordinated in support of this central neurocognitive function. Previously, we showed that working memory for everyday “what,” “where,” and “when” associations depends on multiplexed oscillatory systems, in which signals of different frequencies simultaneously link the PFC to parieto-occipital and medial temporal regions, pointing to a complex web of sub-second, bidirectional interactions. Here, we used direct brain recordings to delineate the frontoparietal oscillatory correlates of working memory with high spatiotemporal precision. Seven intracranial patients with electrodes simultaneously localized to prefrontal and parietal cortices performed a visuospatial working memory task that operationalizes the types of identity and spatiotemporal information we encounter every day. First, task-induced oscillations in the same delta-theta (2–7 Hz) and alpha-beta (9–24 Hz) frequency ranges previously identified using scalp electroencephalography (EEG) carried information about the contents of working memory. Second, maintenance was linked to directional connectivity from the parietal cortex to the PFC. However, presentation of the test prompt to cue identity, spatial, or temporal information changed delta-theta coordination from a unidirectional, parietal-led system to a bidirectional, frontoparietal system. Third, the processing of spatiotemporal information was more bidirectional in the delta-theta range than was the processing of identity information, where alpha-beta connectivity did not exhibit sensitivity to the contents of working memory. These findings implicate a bidirectional delta-theta mechanism for frontoparietal control over the contents of working memory.
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spelling pubmed-63330502019-01-22 Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network Johnson, Elizabeth L. King-Stephens, David Weber, Peter B. Laxer, Kenneth D. Lin, Jack J. Knight, Robert T. Front Syst Neurosci Neuroscience How does the human brain rapidly process incoming information in working memory? In growing divergence from a single-region focus on the prefrontal cortex (PFC), recent work argues for emphasis on how distributed neural networks are rapidly coordinated in support of this central neurocognitive function. Previously, we showed that working memory for everyday “what,” “where,” and “when” associations depends on multiplexed oscillatory systems, in which signals of different frequencies simultaneously link the PFC to parieto-occipital and medial temporal regions, pointing to a complex web of sub-second, bidirectional interactions. Here, we used direct brain recordings to delineate the frontoparietal oscillatory correlates of working memory with high spatiotemporal precision. Seven intracranial patients with electrodes simultaneously localized to prefrontal and parietal cortices performed a visuospatial working memory task that operationalizes the types of identity and spatiotemporal information we encounter every day. First, task-induced oscillations in the same delta-theta (2–7 Hz) and alpha-beta (9–24 Hz) frequency ranges previously identified using scalp electroencephalography (EEG) carried information about the contents of working memory. Second, maintenance was linked to directional connectivity from the parietal cortex to the PFC. However, presentation of the test prompt to cue identity, spatial, or temporal information changed delta-theta coordination from a unidirectional, parietal-led system to a bidirectional, frontoparietal system. Third, the processing of spatiotemporal information was more bidirectional in the delta-theta range than was the processing of identity information, where alpha-beta connectivity did not exhibit sensitivity to the contents of working memory. These findings implicate a bidirectional delta-theta mechanism for frontoparietal control over the contents of working memory. Frontiers Media S.A. 2019-01-08 /pmc/articles/PMC6333050/ /pubmed/30670953 http://dx.doi.org/10.3389/fnsys.2018.00065 Text en Copyright © 2019 Johnson, King-Stephens, Weber, Laxer, Lin and Knight. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Johnson, Elizabeth L.
King-Stephens, David
Weber, Peter B.
Laxer, Kenneth D.
Lin, Jack J.
Knight, Robert T.
Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network
title Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network
title_full Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network
title_fullStr Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network
title_full_unstemmed Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network
title_short Spectral Imprints of Working Memory for Everyday Associations in the Frontoparietal Network
title_sort spectral imprints of working memory for everyday associations in the frontoparietal network
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333050/
https://www.ncbi.nlm.nih.gov/pubmed/30670953
http://dx.doi.org/10.3389/fnsys.2018.00065
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