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Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing
Fluctuations in arousal, controlled by subcortical neuromodulatory systems, continuously shape cortical state, with profound consequences for information processing. Yet, how arousal signals influence cortical population activity in detail has so far only been characterized for a few selected brain...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853659/ https://www.ncbi.nlm.nih.gov/pubmed/35133276 http://dx.doi.org/10.7554/eLife.71890 |
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author | Pfeffer, Thomas Keitel, Christian Kluger, Daniel S Keitel, Anne Russmann, Alena Thut, Gregor Donner, Tobias H Gross, Joachim |
author_facet | Pfeffer, Thomas Keitel, Christian Kluger, Daniel S Keitel, Anne Russmann, Alena Thut, Gregor Donner, Tobias H Gross, Joachim |
author_sort | Pfeffer, Thomas |
collection | PubMed |
description | Fluctuations in arousal, controlled by subcortical neuromodulatory systems, continuously shape cortical state, with profound consequences for information processing. Yet, how arousal signals influence cortical population activity in detail has so far only been characterized for a few selected brain regions. Traditional accounts conceptualize arousal as a homogeneous modulator of neural population activity across the cerebral cortex. Recent insights, however, point to a higher specificity of arousal effects on different components of neural activity and across cortical regions. Here, we provide a comprehensive account of the relationships between fluctuations in arousal and neuronal population activity across the human brain. Exploiting the established link between pupil size and central arousal systems, we performed concurrent magnetoencephalographic (MEG) and pupillographic recordings in a large number of participants, pooled across three laboratories. We found a cascade of effects relative to the peak timing of spontaneous pupil dilations: Decreases in low-frequency (2–8 Hz) activity in temporal and lateral frontal cortex, followed by increased high-frequency (>64 Hz) activity in mid-frontal regions, followed by monotonic and inverted U relationships with intermediate frequency-range activity (8–32 Hz) in occipito-parietal regions. Pupil-linked arousal also coincided with widespread changes in the structure of the aperiodic component of cortical population activity, indicative of changes in the excitation-inhibition balance in underlying microcircuits. Our results provide a novel basis for studying the arousal modulation of cognitive computations in cortical circuits. |
format | Online Article Text |
id | pubmed-8853659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88536592022-02-22 Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing Pfeffer, Thomas Keitel, Christian Kluger, Daniel S Keitel, Anne Russmann, Alena Thut, Gregor Donner, Tobias H Gross, Joachim eLife Neuroscience Fluctuations in arousal, controlled by subcortical neuromodulatory systems, continuously shape cortical state, with profound consequences for information processing. Yet, how arousal signals influence cortical population activity in detail has so far only been characterized for a few selected brain regions. Traditional accounts conceptualize arousal as a homogeneous modulator of neural population activity across the cerebral cortex. Recent insights, however, point to a higher specificity of arousal effects on different components of neural activity and across cortical regions. Here, we provide a comprehensive account of the relationships between fluctuations in arousal and neuronal population activity across the human brain. Exploiting the established link between pupil size and central arousal systems, we performed concurrent magnetoencephalographic (MEG) and pupillographic recordings in a large number of participants, pooled across three laboratories. We found a cascade of effects relative to the peak timing of spontaneous pupil dilations: Decreases in low-frequency (2–8 Hz) activity in temporal and lateral frontal cortex, followed by increased high-frequency (>64 Hz) activity in mid-frontal regions, followed by monotonic and inverted U relationships with intermediate frequency-range activity (8–32 Hz) in occipito-parietal regions. Pupil-linked arousal also coincided with widespread changes in the structure of the aperiodic component of cortical population activity, indicative of changes in the excitation-inhibition balance in underlying microcircuits. Our results provide a novel basis for studying the arousal modulation of cognitive computations in cortical circuits. eLife Sciences Publications, Ltd 2022-02-08 /pmc/articles/PMC8853659/ /pubmed/35133276 http://dx.doi.org/10.7554/eLife.71890 Text en © 2022, Pfeffer, Keitel et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Pfeffer, Thomas Keitel, Christian Kluger, Daniel S Keitel, Anne Russmann, Alena Thut, Gregor Donner, Tobias H Gross, Joachim Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing |
title | Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing |
title_full | Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing |
title_fullStr | Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing |
title_full_unstemmed | Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing |
title_short | Coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing |
title_sort | coupling of pupil- and neuronal population dynamics reveals diverse influences of arousal on cortical processing |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853659/ https://www.ncbi.nlm.nih.gov/pubmed/35133276 http://dx.doi.org/10.7554/eLife.71890 |
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