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Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model

Biophysical models of large-scale brain activity are a fundamental tool for understanding the mechanisms underlying the patterns observed with neuroimaging. These models combine a macroscopic description of the within- and between-ensemble dynamics of neurons within a single architecture. A challeng...

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Autores principales: Portoles, Oscar, Qin, Yuzhen, Hadida, Jonathan, Woolrich, Mark, Cao, Ming, van Vugt, Marieke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604991/
https://www.ncbi.nlm.nih.gov/pubmed/36288273
http://dx.doi.org/10.1371/journal.pone.0275819
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author Portoles, Oscar
Qin, Yuzhen
Hadida, Jonathan
Woolrich, Mark
Cao, Ming
van Vugt, Marieke
author_facet Portoles, Oscar
Qin, Yuzhen
Hadida, Jonathan
Woolrich, Mark
Cao, Ming
van Vugt, Marieke
author_sort Portoles, Oscar
collection PubMed
description Biophysical models of large-scale brain activity are a fundamental tool for understanding the mechanisms underlying the patterns observed with neuroimaging. These models combine a macroscopic description of the within- and between-ensemble dynamics of neurons within a single architecture. A challenge for these models is accounting for modulations of within-ensemble synchrony over time. Such modulations in local synchrony are fundamental for modeling behavioral tasks and resting-state activity. Another challenge comes from the difficulty in parametrizing large scale brain models which hinders researching principles related with between-ensembles differences. Here we derive a parsimonious large scale brain model that can describe fluctuations of local synchrony. Crucially, we do not reduce within-ensemble dynamics to macroscopic variables first, instead we consider within and between-ensemble interactions similarly while preserving their physiological differences. The dynamics of within-ensemble synchrony can be tuned with a parameter which manipulates local connectivity strength. We simulated resting-state static and time-resolved functional connectivity of alpha band envelopes in models with identical and dissimilar local connectivities. We show that functional connectivity emerges when there are high fluctuations of local and global synchrony simultaneously (i.e. metastable dynamics). We also show that for most ensembles, leaning towards local asynchrony or synchrony correlates with the functional connectivity with other ensembles, with the exception of some regions belonging to the default-mode network.
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spelling pubmed-96049912022-10-27 Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model Portoles, Oscar Qin, Yuzhen Hadida, Jonathan Woolrich, Mark Cao, Ming van Vugt, Marieke PLoS One Research Article Biophysical models of large-scale brain activity are a fundamental tool for understanding the mechanisms underlying the patterns observed with neuroimaging. These models combine a macroscopic description of the within- and between-ensemble dynamics of neurons within a single architecture. A challenge for these models is accounting for modulations of within-ensemble synchrony over time. Such modulations in local synchrony are fundamental for modeling behavioral tasks and resting-state activity. Another challenge comes from the difficulty in parametrizing large scale brain models which hinders researching principles related with between-ensembles differences. Here we derive a parsimonious large scale brain model that can describe fluctuations of local synchrony. Crucially, we do not reduce within-ensemble dynamics to macroscopic variables first, instead we consider within and between-ensemble interactions similarly while preserving their physiological differences. The dynamics of within-ensemble synchrony can be tuned with a parameter which manipulates local connectivity strength. We simulated resting-state static and time-resolved functional connectivity of alpha band envelopes in models with identical and dissimilar local connectivities. We show that functional connectivity emerges when there are high fluctuations of local and global synchrony simultaneously (i.e. metastable dynamics). We also show that for most ensembles, leaning towards local asynchrony or synchrony correlates with the functional connectivity with other ensembles, with the exception of some regions belonging to the default-mode network. Public Library of Science 2022-10-26 /pmc/articles/PMC9604991/ /pubmed/36288273 http://dx.doi.org/10.1371/journal.pone.0275819 Text en © 2022 Portoles 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
Portoles, Oscar
Qin, Yuzhen
Hadida, Jonathan
Woolrich, Mark
Cao, Ming
van Vugt, Marieke
Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model
title Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model
title_full Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model
title_fullStr Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model
title_full_unstemmed Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model
title_short Modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model
title_sort modulations of local synchrony over time lead to resting-state functional connectivity in a parsimonious large-scale brain model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604991/
https://www.ncbi.nlm.nih.gov/pubmed/36288273
http://dx.doi.org/10.1371/journal.pone.0275819
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