Cargando…

Metastable brain waves

Traveling patterns of neuronal activity—brain waves—have been observed across a breadth of neuronal recordings, states of awareness, and species, but their emergence in the human brain lacks a firm understanding. Here we analyze the complex nonlinear dynamics that emerge from modeling large-scale sp...

Descripción completa

Detalles Bibliográficos
Autores principales: Roberts, James A., Gollo, Leonardo L., Abeysuriya, Romesh G., Roberts, Gloria, Mitchell, Philip B., Woolrich, Mark W., Breakspear, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401142/
https://www.ncbi.nlm.nih.gov/pubmed/30837462
http://dx.doi.org/10.1038/s41467-019-08999-0
_version_ 1783400102930415616
author Roberts, James A.
Gollo, Leonardo L.
Abeysuriya, Romesh G.
Roberts, Gloria
Mitchell, Philip B.
Woolrich, Mark W.
Breakspear, Michael
author_facet Roberts, James A.
Gollo, Leonardo L.
Abeysuriya, Romesh G.
Roberts, Gloria
Mitchell, Philip B.
Woolrich, Mark W.
Breakspear, Michael
author_sort Roberts, James A.
collection PubMed
description Traveling patterns of neuronal activity—brain waves—have been observed across a breadth of neuronal recordings, states of awareness, and species, but their emergence in the human brain lacks a firm understanding. Here we analyze the complex nonlinear dynamics that emerge from modeling large-scale spontaneous neural activity on a whole-brain network derived from human tractography. We find a rich array of three-dimensional wave patterns, including traveling waves, spiral waves, sources, and sinks. These patterns are metastable, such that multiple spatiotemporal wave patterns are visited in sequence. Transitions between states correspond to reconfigurations of underlying phase flows, characterized by nonlinear instabilities. These metastable dynamics accord with empirical data from multiple imaging modalities, including electrical waves in cortical tissue, sequential spatiotemporal patterns in resting-state MEG data, and large-scale waves in human electrocorticography. By moving the study of functional networks from a spatially static to an inherently dynamic (wave-like) frame, our work unifies apparently diverse phenomena across functional neuroimaging modalities and makes specific predictions for further experimentation.
format Online
Article
Text
id pubmed-6401142
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-64011422019-03-18 Metastable brain waves Roberts, James A. Gollo, Leonardo L. Abeysuriya, Romesh G. Roberts, Gloria Mitchell, Philip B. Woolrich, Mark W. Breakspear, Michael Nat Commun Article Traveling patterns of neuronal activity—brain waves—have been observed across a breadth of neuronal recordings, states of awareness, and species, but their emergence in the human brain lacks a firm understanding. Here we analyze the complex nonlinear dynamics that emerge from modeling large-scale spontaneous neural activity on a whole-brain network derived from human tractography. We find a rich array of three-dimensional wave patterns, including traveling waves, spiral waves, sources, and sinks. These patterns are metastable, such that multiple spatiotemporal wave patterns are visited in sequence. Transitions between states correspond to reconfigurations of underlying phase flows, characterized by nonlinear instabilities. These metastable dynamics accord with empirical data from multiple imaging modalities, including electrical waves in cortical tissue, sequential spatiotemporal patterns in resting-state MEG data, and large-scale waves in human electrocorticography. By moving the study of functional networks from a spatially static to an inherently dynamic (wave-like) frame, our work unifies apparently diverse phenomena across functional neuroimaging modalities and makes specific predictions for further experimentation. Nature Publishing Group UK 2019-03-05 /pmc/articles/PMC6401142/ /pubmed/30837462 http://dx.doi.org/10.1038/s41467-019-08999-0 Text en © The Author(s) 2019 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
Roberts, James A.
Gollo, Leonardo L.
Abeysuriya, Romesh G.
Roberts, Gloria
Mitchell, Philip B.
Woolrich, Mark W.
Breakspear, Michael
Metastable brain waves
title Metastable brain waves
title_full Metastable brain waves
title_fullStr Metastable brain waves
title_full_unstemmed Metastable brain waves
title_short Metastable brain waves
title_sort metastable brain waves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401142/
https://www.ncbi.nlm.nih.gov/pubmed/30837462
http://dx.doi.org/10.1038/s41467-019-08999-0
work_keys_str_mv AT robertsjamesa metastablebrainwaves
AT golloleonardol metastablebrainwaves
AT abeysuriyaromeshg metastablebrainwaves
AT robertsgloria metastablebrainwaves
AT mitchellphilipb metastablebrainwaves
AT woolrichmarkw metastablebrainwaves
AT breakspearmichael metastablebrainwaves