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Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance

Neuronal activity in sensory and fronto-parietal (FP) areas underlies the representation and attentional control, respectively, of sensory information maintained in visual working memory (VWM). Within these regions, beta/gamma phase-synchronization supports the integration of sensory functions, whil...

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Autores principales: Siebenhühner, Felix, Wang, Sheng H, Palva, J Matias, Palva, Satu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070951/
https://www.ncbi.nlm.nih.gov/pubmed/27669146
http://dx.doi.org/10.7554/eLife.13451
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author Siebenhühner, Felix
Wang, Sheng H
Palva, J Matias
Palva, Satu
author_facet Siebenhühner, Felix
Wang, Sheng H
Palva, J Matias
Palva, Satu
author_sort Siebenhühner, Felix
collection PubMed
description Neuronal activity in sensory and fronto-parietal (FP) areas underlies the representation and attentional control, respectively, of sensory information maintained in visual working memory (VWM). Within these regions, beta/gamma phase-synchronization supports the integration of sensory functions, while synchronization in theta/alpha bands supports the regulation of attentional functions. A key challenge is to understand which mechanisms integrate neuronal processing across these distinct frequencies and thereby the sensory and attentional functions. We investigated whether such integration could be achieved by cross-frequency phase synchrony (CFS). Using concurrent magneto- and electroencephalography, we found that CFS was load-dependently enhanced between theta and alpha–gamma and between alpha and beta-gamma oscillations during VWM maintenance among visual, FP, and dorsal attention (DA) systems. CFS also connected the hubs of within-frequency-synchronized networks and its strength predicted individual VWM capacity. We propose that CFS integrates processing among synchronized neuronal networks from theta to gamma frequencies to link sensory and attentional functions. DOI: http://dx.doi.org/10.7554/eLife.13451.001
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spelling pubmed-50709512016-10-20 Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance Siebenhühner, Felix Wang, Sheng H Palva, J Matias Palva, Satu eLife Neuroscience Neuronal activity in sensory and fronto-parietal (FP) areas underlies the representation and attentional control, respectively, of sensory information maintained in visual working memory (VWM). Within these regions, beta/gamma phase-synchronization supports the integration of sensory functions, while synchronization in theta/alpha bands supports the regulation of attentional functions. A key challenge is to understand which mechanisms integrate neuronal processing across these distinct frequencies and thereby the sensory and attentional functions. We investigated whether such integration could be achieved by cross-frequency phase synchrony (CFS). Using concurrent magneto- and electroencephalography, we found that CFS was load-dependently enhanced between theta and alpha–gamma and between alpha and beta-gamma oscillations during VWM maintenance among visual, FP, and dorsal attention (DA) systems. CFS also connected the hubs of within-frequency-synchronized networks and its strength predicted individual VWM capacity. We propose that CFS integrates processing among synchronized neuronal networks from theta to gamma frequencies to link sensory and attentional functions. DOI: http://dx.doi.org/10.7554/eLife.13451.001 eLife Sciences Publications, Ltd 2016-09-26 /pmc/articles/PMC5070951/ /pubmed/27669146 http://dx.doi.org/10.7554/eLife.13451 Text en © 2016, Siebenhühner et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Siebenhühner, Felix
Wang, Sheng H
Palva, J Matias
Palva, Satu
Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance
title Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance
title_full Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance
title_fullStr Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance
title_full_unstemmed Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance
title_short Cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance
title_sort cross-frequency synchronization connects networks of fast and slow oscillations during visual working memory maintenance
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070951/
https://www.ncbi.nlm.nih.gov/pubmed/27669146
http://dx.doi.org/10.7554/eLife.13451
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