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Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks

Frequency-specific oscillations and phase-coupling of neuronal populations are essential mechanisms for the coordination of activity between brain areas during cognitive tasks. Therefore, the ongoing activity ascribed to the different functional brain networks should also be able to reorganise and c...

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Autores principales: Vidaurre, Diego, Hunt, Laurence T., Quinn, Andrew J., Hunt, Benjamin A. E., Brookes, Matthew J., Nobre, Anna C., Woolrich, Mark W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065434/
https://www.ncbi.nlm.nih.gov/pubmed/30061566
http://dx.doi.org/10.1038/s41467-018-05316-z
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author Vidaurre, Diego
Hunt, Laurence T.
Quinn, Andrew J.
Hunt, Benjamin A. E.
Brookes, Matthew J.
Nobre, Anna C.
Woolrich, Mark W.
author_facet Vidaurre, Diego
Hunt, Laurence T.
Quinn, Andrew J.
Hunt, Benjamin A. E.
Brookes, Matthew J.
Nobre, Anna C.
Woolrich, Mark W.
author_sort Vidaurre, Diego
collection PubMed
description Frequency-specific oscillations and phase-coupling of neuronal populations are essential mechanisms for the coordination of activity between brain areas during cognitive tasks. Therefore, the ongoing activity ascribed to the different functional brain networks should also be able to reorganise and coordinate via similar mechanisms. We develop a novel method for identifying large-scale phase-coupled network dynamics and show that resting networks in magnetoencephalography are well characterised by visits to short-lived transient brain states, with spatially distinct patterns of oscillatory power and coherence in specific frequency bands. Brain states are identified for sensory, motor networks and higher-order cognitive networks. The cognitive networks include a posterior alpha (8–12 Hz) and an anterior delta/theta range (1–7 Hz) network, both exhibiting high power and coherence in areas that correspond to posterior and anterior subdivisions of the default mode network. Our results show that large-scale cortical phase-coupling networks have characteristic signatures in very specific frequency bands, possibly reflecting functional specialisation at different intrinsic timescales.
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spelling pubmed-60654342018-07-31 Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks Vidaurre, Diego Hunt, Laurence T. Quinn, Andrew J. Hunt, Benjamin A. E. Brookes, Matthew J. Nobre, Anna C. Woolrich, Mark W. Nat Commun Article Frequency-specific oscillations and phase-coupling of neuronal populations are essential mechanisms for the coordination of activity between brain areas during cognitive tasks. Therefore, the ongoing activity ascribed to the different functional brain networks should also be able to reorganise and coordinate via similar mechanisms. We develop a novel method for identifying large-scale phase-coupled network dynamics and show that resting networks in magnetoencephalography are well characterised by visits to short-lived transient brain states, with spatially distinct patterns of oscillatory power and coherence in specific frequency bands. Brain states are identified for sensory, motor networks and higher-order cognitive networks. The cognitive networks include a posterior alpha (8–12 Hz) and an anterior delta/theta range (1–7 Hz) network, both exhibiting high power and coherence in areas that correspond to posterior and anterior subdivisions of the default mode network. Our results show that large-scale cortical phase-coupling networks have characteristic signatures in very specific frequency bands, possibly reflecting functional specialisation at different intrinsic timescales. Nature Publishing Group UK 2018-07-30 /pmc/articles/PMC6065434/ /pubmed/30061566 http://dx.doi.org/10.1038/s41467-018-05316-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Vidaurre, Diego
Hunt, Laurence T.
Quinn, Andrew J.
Hunt, Benjamin A. E.
Brookes, Matthew J.
Nobre, Anna C.
Woolrich, Mark W.
Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
title Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
title_full Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
title_fullStr Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
title_full_unstemmed Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
title_short Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
title_sort spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065434/
https://www.ncbi.nlm.nih.gov/pubmed/30061566
http://dx.doi.org/10.1038/s41467-018-05316-z
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