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Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy
A critical component of anesthesia is the loss sensory perception. Propofol is the most widely used drug for general anesthesia, but the neural mechanisms of how and when it disrupts sensory processing are not fully understood. We analyzed local field potential (LFP) and spiking recorded from Utah a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327085/ https://www.ncbi.nlm.nih.gov/pubmed/37425684 http://dx.doi.org/10.1101/2023.06.25.546463 |
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author | Tauber, John M. Brincat, Scott L. Stephen, Emily P. Donaghue, Jacob A. Kozachkov, Leo Brown, Emery N. Miller, Earl K. |
author_facet | Tauber, John M. Brincat, Scott L. Stephen, Emily P. Donaghue, Jacob A. Kozachkov, Leo Brown, Emery N. Miller, Earl K. |
author_sort | Tauber, John M. |
collection | PubMed |
description | A critical component of anesthesia is the loss sensory perception. Propofol is the most widely used drug for general anesthesia, but the neural mechanisms of how and when it disrupts sensory processing are not fully understood. We analyzed local field potential (LFP) and spiking recorded from Utah arrays in auditory cortex, associative cortex, and cognitive cortex of non-human primates before and during propofol mediated unconsciousness. Sensory stimuli elicited robust and decodable stimulus responses and triggered periods of stimulus-induced coherence between brain areas in the LFP of awake animals. By contrast, propofol mediated unconsciousness eliminated stimulus-induced coherence and drastically weakened stimulus responses and information in all brain areas except for auditory cortex, where responses and information persisted. However, we found stimuli occurring during spiking Up states triggered weaker spiking responses than in awake animals in auditory cortex, and little or no spiking responses in higher order areas. These results suggest that propofol’s effect on sensory processing is not just due to asynchronous down states. Rather, both Down states and Up states reflect disrupted dynamics. |
format | Online Article Text |
id | pubmed-10327085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103270852023-07-08 Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy Tauber, John M. Brincat, Scott L. Stephen, Emily P. Donaghue, Jacob A. Kozachkov, Leo Brown, Emery N. Miller, Earl K. bioRxiv Article A critical component of anesthesia is the loss sensory perception. Propofol is the most widely used drug for general anesthesia, but the neural mechanisms of how and when it disrupts sensory processing are not fully understood. We analyzed local field potential (LFP) and spiking recorded from Utah arrays in auditory cortex, associative cortex, and cognitive cortex of non-human primates before and during propofol mediated unconsciousness. Sensory stimuli elicited robust and decodable stimulus responses and triggered periods of stimulus-induced coherence between brain areas in the LFP of awake animals. By contrast, propofol mediated unconsciousness eliminated stimulus-induced coherence and drastically weakened stimulus responses and information in all brain areas except for auditory cortex, where responses and information persisted. However, we found stimuli occurring during spiking Up states triggered weaker spiking responses than in awake animals in auditory cortex, and little or no spiking responses in higher order areas. These results suggest that propofol’s effect on sensory processing is not just due to asynchronous down states. Rather, both Down states and Up states reflect disrupted dynamics. Cold Spring Harbor Laboratory 2023-06-29 /pmc/articles/PMC10327085/ /pubmed/37425684 http://dx.doi.org/10.1101/2023.06.25.546463 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Tauber, John M. Brincat, Scott L. Stephen, Emily P. Donaghue, Jacob A. Kozachkov, Leo Brown, Emery N. Miller, Earl K. Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy |
title | Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy |
title_full | Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy |
title_fullStr | Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy |
title_full_unstemmed | Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy |
title_short | Propofol Mediated Unconsciousness Disrupts Progression of Sensory Signals through the Cortical Hierarchy |
title_sort | propofol mediated unconsciousness disrupts progression of sensory signals through the cortical hierarchy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327085/ https://www.ncbi.nlm.nih.gov/pubmed/37425684 http://dx.doi.org/10.1101/2023.06.25.546463 |
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