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Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states

The human brain displays a rich repertoire of states that emerge from the microscopic interactions of cortical and subcortical neurons. Difficulties inherent within large-scale simultaneous neuronal recording limit our ability to link biophysical processes at the microscale to emergent macroscopic b...

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Autores principales: Munn, Brandon R., Müller, Eli J., Medel, Vicente, Naismith, Sharon L., Lizier, Joseph T., Sanders, Robert D., Shine, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10611774/
https://www.ncbi.nlm.nih.gov/pubmed/37891167
http://dx.doi.org/10.1038/s41467-023-42465-2
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author Munn, Brandon R.
Müller, Eli J.
Medel, Vicente
Naismith, Sharon L.
Lizier, Joseph T.
Sanders, Robert D.
Shine, James M.
author_facet Munn, Brandon R.
Müller, Eli J.
Medel, Vicente
Naismith, Sharon L.
Lizier, Joseph T.
Sanders, Robert D.
Shine, James M.
author_sort Munn, Brandon R.
collection PubMed
description The human brain displays a rich repertoire of states that emerge from the microscopic interactions of cortical and subcortical neurons. Difficulties inherent within large-scale simultaneous neuronal recording limit our ability to link biophysical processes at the microscale to emergent macroscopic brain states. Here we introduce a microscale biophysical network model of layer-5 pyramidal neurons that display graded coarse-sampled dynamics matching those observed in macroscale electrophysiological recordings from macaques and humans. We invert our model to identify the neuronal spike and burst dynamics that differentiate unconscious, dreaming, and awake arousal states and provide insights into their functional signatures. We further show that neuromodulatory arousal can mediate different modes of neuronal dynamics around a low-dimensional energy landscape, which in turn changes the response of the model to external stimuli. Our results highlight the promise of multiscale modelling to bridge theories of consciousness across spatiotemporal scales.
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spelling pubmed-106117742023-10-29 Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states Munn, Brandon R. Müller, Eli J. Medel, Vicente Naismith, Sharon L. Lizier, Joseph T. Sanders, Robert D. Shine, James M. Nat Commun Article The human brain displays a rich repertoire of states that emerge from the microscopic interactions of cortical and subcortical neurons. Difficulties inherent within large-scale simultaneous neuronal recording limit our ability to link biophysical processes at the microscale to emergent macroscopic brain states. Here we introduce a microscale biophysical network model of layer-5 pyramidal neurons that display graded coarse-sampled dynamics matching those observed in macroscale electrophysiological recordings from macaques and humans. We invert our model to identify the neuronal spike and burst dynamics that differentiate unconscious, dreaming, and awake arousal states and provide insights into their functional signatures. We further show that neuromodulatory arousal can mediate different modes of neuronal dynamics around a low-dimensional energy landscape, which in turn changes the response of the model to external stimuli. Our results highlight the promise of multiscale modelling to bridge theories of consciousness across spatiotemporal scales. Nature Publishing Group UK 2023-10-27 /pmc/articles/PMC10611774/ /pubmed/37891167 http://dx.doi.org/10.1038/s41467-023-42465-2 Text en © Crown 2023 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
Munn, Brandon R.
Müller, Eli J.
Medel, Vicente
Naismith, Sharon L.
Lizier, Joseph T.
Sanders, Robert D.
Shine, James M.
Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states
title Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states
title_full Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states
title_fullStr Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states
title_full_unstemmed Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states
title_short Neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states
title_sort neuronal connected burst cascades bridge macroscale adaptive signatures across arousal states
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10611774/
https://www.ncbi.nlm.nih.gov/pubmed/37891167
http://dx.doi.org/10.1038/s41467-023-42465-2
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