Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1785128556934725632 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10611774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT munnbrandonr neuronalconnectedburstcascadesbridgemacroscaleadaptivesignaturesacrossarousalstates AT mullerelij neuronalconnectedburstcascadesbridgemacroscaleadaptivesignaturesacrossarousalstates AT medelvicente neuronalconnectedburstcascadesbridgemacroscaleadaptivesignaturesacrossarousalstates AT naismithsharonl neuronalconnectedburstcascadesbridgemacroscaleadaptivesignaturesacrossarousalstates AT lizierjosepht neuronalconnectedburstcascadesbridgemacroscaleadaptivesignaturesacrossarousalstates AT sandersrobertd neuronalconnectedburstcascadesbridgemacroscaleadaptivesignaturesacrossarousalstates AT shinejamesm neuronalconnectedburstcascadesbridgemacroscaleadaptivesignaturesacrossarousalstates |