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Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks

Spatiotemporal oscillations underlie all cognitive brain functions. Large-scale brain models, constrained by neuroimaging data, aim to trace the principles underlying such macroscopic neural activity from the intricate and multi-scale structure of the brain. Despite substantial progress in the field...

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Autores principales: Clusella, Pau, Deco, Gustavo, Kringelbach, Morten L., Ruffini, Giulio, Garcia-Ojalvo, Jordi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124884/
https://www.ncbi.nlm.nih.gov/pubmed/37043504
http://dx.doi.org/10.1371/journal.pcbi.1010781
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author Clusella, Pau
Deco, Gustavo
Kringelbach, Morten L.
Ruffini, Giulio
Garcia-Ojalvo, Jordi
author_facet Clusella, Pau
Deco, Gustavo
Kringelbach, Morten L.
Ruffini, Giulio
Garcia-Ojalvo, Jordi
author_sort Clusella, Pau
collection PubMed
description Spatiotemporal oscillations underlie all cognitive brain functions. Large-scale brain models, constrained by neuroimaging data, aim to trace the principles underlying such macroscopic neural activity from the intricate and multi-scale structure of the brain. Despite substantial progress in the field, many aspects about the mechanisms behind the onset of spatiotemporal neural dynamics are still unknown. In this work we establish a simple framework for the emergence of complex brain dynamics, including high-dimensional chaos and travelling waves. The model consists of a complex network of 90 brain regions, whose structural connectivity is obtained from tractography data. The activity of each brain area is governed by a Jansen neural mass model and we normalize the total input received by each node so it amounts the same across all brain areas. This assumption allows for the existence of an homogeneous invariant manifold, i.e., a set of different stationary and oscillatory states in which all nodes behave identically. Stability analysis of these homogeneous solutions unveils a transverse instability of the synchronized state, which gives rise to different types of spatiotemporal dynamics, such as chaotic alpha activity. Additionally, we illustrate the ubiquity of this route towards complex spatiotemporal activity in a network of next generation neural mass models. Altogehter, our results unveil the bifurcation landscape that underlies the emergence of function from structure in the brain.
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spelling pubmed-101248842023-04-25 Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks Clusella, Pau Deco, Gustavo Kringelbach, Morten L. Ruffini, Giulio Garcia-Ojalvo, Jordi PLoS Comput Biol Research Article Spatiotemporal oscillations underlie all cognitive brain functions. Large-scale brain models, constrained by neuroimaging data, aim to trace the principles underlying such macroscopic neural activity from the intricate and multi-scale structure of the brain. Despite substantial progress in the field, many aspects about the mechanisms behind the onset of spatiotemporal neural dynamics are still unknown. In this work we establish a simple framework for the emergence of complex brain dynamics, including high-dimensional chaos and travelling waves. The model consists of a complex network of 90 brain regions, whose structural connectivity is obtained from tractography data. The activity of each brain area is governed by a Jansen neural mass model and we normalize the total input received by each node so it amounts the same across all brain areas. This assumption allows for the existence of an homogeneous invariant manifold, i.e., a set of different stationary and oscillatory states in which all nodes behave identically. Stability analysis of these homogeneous solutions unveils a transverse instability of the synchronized state, which gives rise to different types of spatiotemporal dynamics, such as chaotic alpha activity. Additionally, we illustrate the ubiquity of this route towards complex spatiotemporal activity in a network of next generation neural mass models. Altogehter, our results unveil the bifurcation landscape that underlies the emergence of function from structure in the brain. Public Library of Science 2023-04-12 /pmc/articles/PMC10124884/ /pubmed/37043504 http://dx.doi.org/10.1371/journal.pcbi.1010781 Text en © 2023 Clusella et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Clusella, Pau
Deco, Gustavo
Kringelbach, Morten L.
Ruffini, Giulio
Garcia-Ojalvo, Jordi
Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks
title Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks
title_full Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks
title_fullStr Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks
title_full_unstemmed Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks
title_short Complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks
title_sort complex spatiotemporal oscillations emerge from transverse instabilities in large-scale brain networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124884/
https://www.ncbi.nlm.nih.gov/pubmed/37043504
http://dx.doi.org/10.1371/journal.pcbi.1010781
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