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Inferring multi-scale neural mechanisms with brain network modelling
The neurophysiological processes underlying non-invasive brain activity measurements are incompletely understood. Here, we developed a connectome-based brain network model that integrates individual structural and functional data with neural population dynamics to support multi-scale neurophysiologi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802851/ https://www.ncbi.nlm.nih.gov/pubmed/29308767 http://dx.doi.org/10.7554/eLife.28927 |
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author | Schirner, Michael McIntosh, Anthony Randal Jirsa, Viktor Deco, Gustavo Ritter, Petra |
author_facet | Schirner, Michael McIntosh, Anthony Randal Jirsa, Viktor Deco, Gustavo Ritter, Petra |
author_sort | Schirner, Michael |
collection | PubMed |
description | The neurophysiological processes underlying non-invasive brain activity measurements are incompletely understood. Here, we developed a connectome-based brain network model that integrates individual structural and functional data with neural population dynamics to support multi-scale neurophysiological inference. Simulated populations were linked by structural connectivity and, as a novelty, driven by electroencephalography (EEG) source activity. Simulations not only predicted subjects' individual resting-state functional magnetic resonance imaging (fMRI) time series and spatial network topologies over 20 minutes of activity, but more importantly, they also revealed precise neurophysiological mechanisms that underlie and link six empirical observations from different scales and modalities: (1) resting-state fMRI oscillations, (2) functional connectivity networks, (3) excitation-inhibition balance, (4, 5) inverse relationships between α-rhythms, spike-firing and fMRI on short and long time scales, and (6) fMRI power-law scaling. These findings underscore the potential of this new modelling framework for general inference and integration of neurophysiological knowledge to complement empirical studies. |
format | Online Article Text |
id | pubmed-5802851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58028512018-02-08 Inferring multi-scale neural mechanisms with brain network modelling Schirner, Michael McIntosh, Anthony Randal Jirsa, Viktor Deco, Gustavo Ritter, Petra eLife Computational and Systems Biology The neurophysiological processes underlying non-invasive brain activity measurements are incompletely understood. Here, we developed a connectome-based brain network model that integrates individual structural and functional data with neural population dynamics to support multi-scale neurophysiological inference. Simulated populations were linked by structural connectivity and, as a novelty, driven by electroencephalography (EEG) source activity. Simulations not only predicted subjects' individual resting-state functional magnetic resonance imaging (fMRI) time series and spatial network topologies over 20 minutes of activity, but more importantly, they also revealed precise neurophysiological mechanisms that underlie and link six empirical observations from different scales and modalities: (1) resting-state fMRI oscillations, (2) functional connectivity networks, (3) excitation-inhibition balance, (4, 5) inverse relationships between α-rhythms, spike-firing and fMRI on short and long time scales, and (6) fMRI power-law scaling. These findings underscore the potential of this new modelling framework for general inference and integration of neurophysiological knowledge to complement empirical studies. eLife Sciences Publications, Ltd 2018-01-08 /pmc/articles/PMC5802851/ /pubmed/29308767 http://dx.doi.org/10.7554/eLife.28927 Text en © 2018, Schirner et al http://creativecommons.org/licenses/by/4.0/ 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 | Computational and Systems Biology Schirner, Michael McIntosh, Anthony Randal Jirsa, Viktor Deco, Gustavo Ritter, Petra Inferring multi-scale neural mechanisms with brain network modelling |
title | Inferring multi-scale neural mechanisms with brain network modelling |
title_full | Inferring multi-scale neural mechanisms with brain network modelling |
title_fullStr | Inferring multi-scale neural mechanisms with brain network modelling |
title_full_unstemmed | Inferring multi-scale neural mechanisms with brain network modelling |
title_short | Inferring multi-scale neural mechanisms with brain network modelling |
title_sort | inferring multi-scale neural mechanisms with brain network modelling |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802851/ https://www.ncbi.nlm.nih.gov/pubmed/29308767 http://dx.doi.org/10.7554/eLife.28927 |
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