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Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex

During resting-state EEG recordings, alpha activity is more prominent over the posterior cortex in eyes-closed (EC) conditions compared to eyes-open (EO). In this study, we characterized the difference in spectra between EO and EC conditions using dynamic causal modelling. Specifically, we investiga...

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Autores principales: Van de Steen, Frederik, Pinotsis, Dimitris, Devos, Wouter, Colenbier, Nigel, Bassez, Iege, Friston, Karl, Marinazzo, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829170/
https://www.ncbi.nlm.nih.gov/pubmed/36574458
http://dx.doi.org/10.1371/journal.pcbi.1009988
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author Van de Steen, Frederik
Pinotsis, Dimitris
Devos, Wouter
Colenbier, Nigel
Bassez, Iege
Friston, Karl
Marinazzo, Daniele
author_facet Van de Steen, Frederik
Pinotsis, Dimitris
Devos, Wouter
Colenbier, Nigel
Bassez, Iege
Friston, Karl
Marinazzo, Daniele
author_sort Van de Steen, Frederik
collection PubMed
description During resting-state EEG recordings, alpha activity is more prominent over the posterior cortex in eyes-closed (EC) conditions compared to eyes-open (EO). In this study, we characterized the difference in spectra between EO and EC conditions using dynamic causal modelling. Specifically, we investigated the role of intrinsic and extrinsic connectivity—within the visual cortex—in generating EC-EO alpha power differences over posterior electrodes. The primary visual cortex (V1) and the bilateral middle temporal visual areas (V5) were equipped with bidirectional extrinsic connections using a canonical microcircuit. The states of four intrinsically coupled subpopulations—within each occipital source—were also modelled. Using Bayesian model selection, we tested whether modulations of the intrinsic connections in V1, V5 or extrinsic connections (or a combination thereof) provided the best evidence for the data. In addition, using parametric empirical Bayes (PEB), we estimated group averages under the winning model. Bayesian model selection showed that the winning model contained both extrinsic connectivity modulations, as well as intrinsic connectivity modulations in all sources. The PEB analysis revealed increased extrinsic connectivity during EC. Overall, we found a reduction in the inhibitory intrinsic connections during EC. The results suggest that the intrinsic modulations in V5 played the most important role in producing EC-EO alpha differences, suggesting an intrinsic disinhibition in higher order visual cortex, during EC resting state.
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spelling pubmed-98291702023-01-10 Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex Van de Steen, Frederik Pinotsis, Dimitris Devos, Wouter Colenbier, Nigel Bassez, Iege Friston, Karl Marinazzo, Daniele PLoS Comput Biol Research Article During resting-state EEG recordings, alpha activity is more prominent over the posterior cortex in eyes-closed (EC) conditions compared to eyes-open (EO). In this study, we characterized the difference in spectra between EO and EC conditions using dynamic causal modelling. Specifically, we investigated the role of intrinsic and extrinsic connectivity—within the visual cortex—in generating EC-EO alpha power differences over posterior electrodes. The primary visual cortex (V1) and the bilateral middle temporal visual areas (V5) were equipped with bidirectional extrinsic connections using a canonical microcircuit. The states of four intrinsically coupled subpopulations—within each occipital source—were also modelled. Using Bayesian model selection, we tested whether modulations of the intrinsic connections in V1, V5 or extrinsic connections (or a combination thereof) provided the best evidence for the data. In addition, using parametric empirical Bayes (PEB), we estimated group averages under the winning model. Bayesian model selection showed that the winning model contained both extrinsic connectivity modulations, as well as intrinsic connectivity modulations in all sources. The PEB analysis revealed increased extrinsic connectivity during EC. Overall, we found a reduction in the inhibitory intrinsic connections during EC. The results suggest that the intrinsic modulations in V5 played the most important role in producing EC-EO alpha differences, suggesting an intrinsic disinhibition in higher order visual cortex, during EC resting state. Public Library of Science 2022-12-27 /pmc/articles/PMC9829170/ /pubmed/36574458 http://dx.doi.org/10.1371/journal.pcbi.1009988 Text en © 2022 Van de Steen 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
Van de Steen, Frederik
Pinotsis, Dimitris
Devos, Wouter
Colenbier, Nigel
Bassez, Iege
Friston, Karl
Marinazzo, Daniele
Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex
title Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex
title_full Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex
title_fullStr Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex
title_full_unstemmed Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex
title_short Dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex
title_sort dynamic causal modelling shows a prominent role of local inhibition in alpha power modulation in higher visual cortex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829170/
https://www.ncbi.nlm.nih.gov/pubmed/36574458
http://dx.doi.org/10.1371/journal.pcbi.1009988
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