Cargando…

The modulation of brain network integration and arousal during exploration

There is growing interest in how neuromodulators shape brain networks. Recent neuroimaging studies provide evidence that brainstem arousal systems, such as the locus coeruleus-norepinephrine system (LC-NE), influence functional connectivity and brain network topology, suggesting they have a role in...

Descripción completa

Detalles Bibliográficos
Autores principales: Tardiff, Nathan, Medaglia, John D., Bassett, Danielle S., Thompson-Schill, Sharon L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507424/
https://www.ncbi.nlm.nih.gov/pubmed/34242784
http://dx.doi.org/10.1016/j.neuroimage.2021.118369
_version_ 1784581852446588928
author Tardiff, Nathan
Medaglia, John D.
Bassett, Danielle S.
Thompson-Schill, Sharon L.
author_facet Tardiff, Nathan
Medaglia, John D.
Bassett, Danielle S.
Thompson-Schill, Sharon L.
author_sort Tardiff, Nathan
collection PubMed
description There is growing interest in how neuromodulators shape brain networks. Recent neuroimaging studies provide evidence that brainstem arousal systems, such as the locus coeruleus-norepinephrine system (LC-NE), influence functional connectivity and brain network topology, suggesting they have a role in flexibly reconfiguring brain networks in order to adapt behavior and cognition to environmental demands. To date, however, the relationship between brainstem arousal systems and functional connectivity has not been assessed within the context of a task with an established relationship between arousal and behavior, with most prior studies relying on incidental variations in arousal or pharmacological manipulation and static brain networks constructed over long periods of time. These factors have likely contributed to a heterogeneity of effects across studies. To address these issues, we took advantage of the association between LC-NE-linked arousal and exploration to probe the relationships between exploratory choice, arousal—as measured indirectly via pupil diameter—and brain network dynamics. Exploration in a bandit task was associated with a shift toward fewer, more weakly connected modules that were more segregated in terms of connectivity and topology but more integrated with respect to the diversity of cognitive systems represented in each module. Functional connectivity strength decreased, and changes in connectivity were correlated with changes in pupil diameter, in line with the hypothesis that brainstem arousal systems influence the dynamic reorganization of brain networks. More broadly, we argue that carefully aligning dynamic network analyses with task designs can increase the temporal resolution at which behaviorally- and cognitively-relevant modulations can be identified, and offer these results as a proof of concept of this approach.
format Online
Article
Text
id pubmed-8507424
institution National Center for Biotechnology Information
language English
publishDate 2021
record_format MEDLINE/PubMed
spelling pubmed-85074242021-10-15 The modulation of brain network integration and arousal during exploration Tardiff, Nathan Medaglia, John D. Bassett, Danielle S. Thompson-Schill, Sharon L. Neuroimage Article There is growing interest in how neuromodulators shape brain networks. Recent neuroimaging studies provide evidence that brainstem arousal systems, such as the locus coeruleus-norepinephrine system (LC-NE), influence functional connectivity and brain network topology, suggesting they have a role in flexibly reconfiguring brain networks in order to adapt behavior and cognition to environmental demands. To date, however, the relationship between brainstem arousal systems and functional connectivity has not been assessed within the context of a task with an established relationship between arousal and behavior, with most prior studies relying on incidental variations in arousal or pharmacological manipulation and static brain networks constructed over long periods of time. These factors have likely contributed to a heterogeneity of effects across studies. To address these issues, we took advantage of the association between LC-NE-linked arousal and exploration to probe the relationships between exploratory choice, arousal—as measured indirectly via pupil diameter—and brain network dynamics. Exploration in a bandit task was associated with a shift toward fewer, more weakly connected modules that were more segregated in terms of connectivity and topology but more integrated with respect to the diversity of cognitive systems represented in each module. Functional connectivity strength decreased, and changes in connectivity were correlated with changes in pupil diameter, in line with the hypothesis that brainstem arousal systems influence the dynamic reorganization of brain networks. More broadly, we argue that carefully aligning dynamic network analyses with task designs can increase the temporal resolution at which behaviorally- and cognitively-relevant modulations can be identified, and offer these results as a proof of concept of this approach. 2021-07-06 2021-10-15 /pmc/articles/PMC8507424/ /pubmed/34242784 http://dx.doi.org/10.1016/j.neuroimage.2021.118369 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Article
Tardiff, Nathan
Medaglia, John D.
Bassett, Danielle S.
Thompson-Schill, Sharon L.
The modulation of brain network integration and arousal during exploration
title The modulation of brain network integration and arousal during exploration
title_full The modulation of brain network integration and arousal during exploration
title_fullStr The modulation of brain network integration and arousal during exploration
title_full_unstemmed The modulation of brain network integration and arousal during exploration
title_short The modulation of brain network integration and arousal during exploration
title_sort modulation of brain network integration and arousal during exploration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507424/
https://www.ncbi.nlm.nih.gov/pubmed/34242784
http://dx.doi.org/10.1016/j.neuroimage.2021.118369
work_keys_str_mv AT tardiffnathan themodulationofbrainnetworkintegrationandarousalduringexploration
AT medagliajohnd themodulationofbrainnetworkintegrationandarousalduringexploration
AT bassettdanielles themodulationofbrainnetworkintegrationandarousalduringexploration
AT thompsonschillsharonl themodulationofbrainnetworkintegrationandarousalduringexploration
AT tardiffnathan modulationofbrainnetworkintegrationandarousalduringexploration
AT medagliajohnd modulationofbrainnetworkintegrationandarousalduringexploration
AT bassettdanielles modulationofbrainnetworkintegrationandarousalduringexploration
AT thompsonschillsharonl modulationofbrainnetworkintegrationandarousalduringexploration