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Dynamic relationships between spontaneous and evoked electrophysiological activity
Spontaneous neural activity fluctuations have been shown to influence trial-by-trial variation in perceptual, cognitive, and behavioral outcomes. However, the complex electrophysiological mechanisms by which these fluctuations shape stimulus-evoked neural activity remain largely to be explored. Empl...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206204/ https://www.ncbi.nlm.nih.gov/pubmed/34131279 http://dx.doi.org/10.1038/s42003-021-02240-9 |
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author | Wainio-Theberge, Soren Wolff, Annemarie Northoff, Georg |
author_facet | Wainio-Theberge, Soren Wolff, Annemarie Northoff, Georg |
author_sort | Wainio-Theberge, Soren |
collection | PubMed |
description | Spontaneous neural activity fluctuations have been shown to influence trial-by-trial variation in perceptual, cognitive, and behavioral outcomes. However, the complex electrophysiological mechanisms by which these fluctuations shape stimulus-evoked neural activity remain largely to be explored. Employing a large-scale magnetoencephalographic dataset and an electroencephalographic replication dataset, we investigate the relationship between spontaneous and evoked neural activity across a range of electrophysiological variables. We observe that for high-frequency activity, high pre-stimulus amplitudes lead to greater evoked desynchronization, while for low frequencies, high pre-stimulus amplitudes induce larger degrees of event-related synchronization. We further decompose electrophysiological power into oscillatory and scale-free components, demonstrating different patterns of spontaneous-evoked correlation for each component. Finally, we find correlations between spontaneous and evoked time-domain electrophysiological signals. Overall, we demonstrate that the dynamics of multiple electrophysiological variables exhibit distinct relationships between their spontaneous and evoked activity, a result which carries implications for experimental design and analysis in non-invasive electrophysiology. |
format | Online Article Text |
id | pubmed-8206204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82062042021-07-01 Dynamic relationships between spontaneous and evoked electrophysiological activity Wainio-Theberge, Soren Wolff, Annemarie Northoff, Georg Commun Biol Article Spontaneous neural activity fluctuations have been shown to influence trial-by-trial variation in perceptual, cognitive, and behavioral outcomes. However, the complex electrophysiological mechanisms by which these fluctuations shape stimulus-evoked neural activity remain largely to be explored. Employing a large-scale magnetoencephalographic dataset and an electroencephalographic replication dataset, we investigate the relationship between spontaneous and evoked neural activity across a range of electrophysiological variables. We observe that for high-frequency activity, high pre-stimulus amplitudes lead to greater evoked desynchronization, while for low frequencies, high pre-stimulus amplitudes induce larger degrees of event-related synchronization. We further decompose electrophysiological power into oscillatory and scale-free components, demonstrating different patterns of spontaneous-evoked correlation for each component. Finally, we find correlations between spontaneous and evoked time-domain electrophysiological signals. Overall, we demonstrate that the dynamics of multiple electrophysiological variables exhibit distinct relationships between their spontaneous and evoked activity, a result which carries implications for experimental design and analysis in non-invasive electrophysiology. Nature Publishing Group UK 2021-06-15 /pmc/articles/PMC8206204/ /pubmed/34131279 http://dx.doi.org/10.1038/s42003-021-02240-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wainio-Theberge, Soren Wolff, Annemarie Northoff, Georg Dynamic relationships between spontaneous and evoked electrophysiological activity |
title | Dynamic relationships between spontaneous and evoked electrophysiological activity |
title_full | Dynamic relationships between spontaneous and evoked electrophysiological activity |
title_fullStr | Dynamic relationships between spontaneous and evoked electrophysiological activity |
title_full_unstemmed | Dynamic relationships between spontaneous and evoked electrophysiological activity |
title_short | Dynamic relationships between spontaneous and evoked electrophysiological activity |
title_sort | dynamic relationships between spontaneous and evoked electrophysiological activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206204/ https://www.ncbi.nlm.nih.gov/pubmed/34131279 http://dx.doi.org/10.1038/s42003-021-02240-9 |
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