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Asymmetric neural dynamics characterize loss and recovery of consciousness()

Anesthetics are known to disrupt neural interactions in cortical and subcortical brain circuits. While the effect of anesthetic drugs on consciousness is reversible, the neural mechanism mediating induction and recovery may be different. Insight into these distinct mechanisms can be gained from a sy...

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Autores principales: Huang, Zirui, Tarnal, Vijay, Vlisides, Phillip E., Janke, Ellen L., McKinney, Amy M., Picton, Paul, Mashour, George A., Hudetz, Anthony G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310457/
https://www.ncbi.nlm.nih.gov/pubmed/33848623
http://dx.doi.org/10.1016/j.neuroimage.2021.118042
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author Huang, Zirui
Tarnal, Vijay
Vlisides, Phillip E.
Janke, Ellen L.
McKinney, Amy M.
Picton, Paul
Mashour, George A.
Hudetz, Anthony G.
author_facet Huang, Zirui
Tarnal, Vijay
Vlisides, Phillip E.
Janke, Ellen L.
McKinney, Amy M.
Picton, Paul
Mashour, George A.
Hudetz, Anthony G.
author_sort Huang, Zirui
collection PubMed
description Anesthetics are known to disrupt neural interactions in cortical and subcortical brain circuits. While the effect of anesthetic drugs on consciousness is reversible, the neural mechanism mediating induction and recovery may be different. Insight into these distinct mechanisms can be gained from a systematic comparison of neural dynamics during slow induction of and emergence from anesthesia. To this end, we used functional magnetic resonance imaging (fMRI) data obtained in healthy volunteers before, during, and after the administration of propofol at incrementally adjusted target concentrations. We analyzed functional connectivity of corticocortical and subcorticocortical networks and the temporal autocorrelation of fMRI signal as an index of neural processing timescales. We found that en route to unconsciousness, temporal autocorrelation across the entire brain gradually increased, whereas functional connectivity gradually decreased. In contrast, regaining consciousness was associated with an abrupt restoration of cortical but not subcortical temporal autocorrelation and an abrupt boost of subcorticocortical functional connectivity. Pharmacokinetic effects could not account for the difference in neural dynamics between induction and emergence. We conclude that the induction and recovery phases of anesthesia follow asymmetric neural dynamics. A rapid increase in the speed of cortical neural processing and subcorticocortical neural interactions may be a mechanism that reboots consciousness.
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spelling pubmed-83104572021-08-01 Asymmetric neural dynamics characterize loss and recovery of consciousness() Huang, Zirui Tarnal, Vijay Vlisides, Phillip E. Janke, Ellen L. McKinney, Amy M. Picton, Paul Mashour, George A. Hudetz, Anthony G. Neuroimage Article Anesthetics are known to disrupt neural interactions in cortical and subcortical brain circuits. While the effect of anesthetic drugs on consciousness is reversible, the neural mechanism mediating induction and recovery may be different. Insight into these distinct mechanisms can be gained from a systematic comparison of neural dynamics during slow induction of and emergence from anesthesia. To this end, we used functional magnetic resonance imaging (fMRI) data obtained in healthy volunteers before, during, and after the administration of propofol at incrementally adjusted target concentrations. We analyzed functional connectivity of corticocortical and subcorticocortical networks and the temporal autocorrelation of fMRI signal as an index of neural processing timescales. We found that en route to unconsciousness, temporal autocorrelation across the entire brain gradually increased, whereas functional connectivity gradually decreased. In contrast, regaining consciousness was associated with an abrupt restoration of cortical but not subcortical temporal autocorrelation and an abrupt boost of subcorticocortical functional connectivity. Pharmacokinetic effects could not account for the difference in neural dynamics between induction and emergence. We conclude that the induction and recovery phases of anesthesia follow asymmetric neural dynamics. A rapid increase in the speed of cortical neural processing and subcorticocortical neural interactions may be a mechanism that reboots consciousness. 2021-04-10 2021-08-01 /pmc/articles/PMC8310457/ /pubmed/33848623 http://dx.doi.org/10.1016/j.neuroimage.2021.118042 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
Huang, Zirui
Tarnal, Vijay
Vlisides, Phillip E.
Janke, Ellen L.
McKinney, Amy M.
Picton, Paul
Mashour, George A.
Hudetz, Anthony G.
Asymmetric neural dynamics characterize loss and recovery of consciousness()
title Asymmetric neural dynamics characterize loss and recovery of consciousness()
title_full Asymmetric neural dynamics characterize loss and recovery of consciousness()
title_fullStr Asymmetric neural dynamics characterize loss and recovery of consciousness()
title_full_unstemmed Asymmetric neural dynamics characterize loss and recovery of consciousness()
title_short Asymmetric neural dynamics characterize loss and recovery of consciousness()
title_sort asymmetric neural dynamics characterize loss and recovery of consciousness()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310457/
https://www.ncbi.nlm.nih.gov/pubmed/33848623
http://dx.doi.org/10.1016/j.neuroimage.2021.118042
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