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The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening

Placing a patient in a state of anaesthesia is crucial for modern surgical practice. However, the mechanisms by which anaesthetic drugs, such as propofol, impart their effects on consciousness remain poorly understood. Propofol potentiates GABAergic transmission, which purportedly has direct actions...

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Autores principales: Lawn, Timothy, Martins, Daniel, O'Daly, Owen, Williams, Steve, Howard, Matthew, Dipasquale, Ottavia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410200/
https://www.ncbi.nlm.nih.gov/pubmed/36935083
http://dx.doi.org/10.1016/j.neuroimage.2023.120018
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author Lawn, Timothy
Martins, Daniel
O'Daly, Owen
Williams, Steve
Howard, Matthew
Dipasquale, Ottavia
author_facet Lawn, Timothy
Martins, Daniel
O'Daly, Owen
Williams, Steve
Howard, Matthew
Dipasquale, Ottavia
author_sort Lawn, Timothy
collection PubMed
description Placing a patient in a state of anaesthesia is crucial for modern surgical practice. However, the mechanisms by which anaesthetic drugs, such as propofol, impart their effects on consciousness remain poorly understood. Propofol potentiates GABAergic transmission, which purportedly has direct actions on cortex as well as indirect actions via ascending neuromodulatory systems. Functional imaging studies to date have been limited in their ability to unravel how these effects on neurotransmission impact the system-level dynamics of the brain. Here, we leveraged advances in multi-modal imaging, Receptor-Enriched Analysis of functional Connectivity by Targets (REACT), to investigate how different levels of propofol-induced sedation alter neurotransmission-related functional connectivity (FC), both at rest and when individuals are exposed to naturalistic auditory stimulation. Propofol increased GABA-A- and noradrenaline transporter-enriched FC within occipital and somatosensory regions respectively. Additionally, during auditory stimulation, the network related to the dopamine transporter showed reduced FC within bilateral regions of temporal and mid/posterior cingulate cortices, with the right temporal cluster showing an interaction between auditory stimulation and level of consciousness. In bringing together these micro- and macro-scale systems, we provide support for both direct GABAergic and indirect noradrenergic and dopaminergic-related network changes under propofol sedation. Further, we delineate a cognition-related reconfiguration of the dopaminergic network, highlighting the utility of REACT to explore the molecular substrates of consciousness and cognition.
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spelling pubmed-104102002023-08-10 The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening Lawn, Timothy Martins, Daniel O'Daly, Owen Williams, Steve Howard, Matthew Dipasquale, Ottavia Neuroimage Article Placing a patient in a state of anaesthesia is crucial for modern surgical practice. However, the mechanisms by which anaesthetic drugs, such as propofol, impart their effects on consciousness remain poorly understood. Propofol potentiates GABAergic transmission, which purportedly has direct actions on cortex as well as indirect actions via ascending neuromodulatory systems. Functional imaging studies to date have been limited in their ability to unravel how these effects on neurotransmission impact the system-level dynamics of the brain. Here, we leveraged advances in multi-modal imaging, Receptor-Enriched Analysis of functional Connectivity by Targets (REACT), to investigate how different levels of propofol-induced sedation alter neurotransmission-related functional connectivity (FC), both at rest and when individuals are exposed to naturalistic auditory stimulation. Propofol increased GABA-A- and noradrenaline transporter-enriched FC within occipital and somatosensory regions respectively. Additionally, during auditory stimulation, the network related to the dopamine transporter showed reduced FC within bilateral regions of temporal and mid/posterior cingulate cortices, with the right temporal cluster showing an interaction between auditory stimulation and level of consciousness. In bringing together these micro- and macro-scale systems, we provide support for both direct GABAergic and indirect noradrenergic and dopaminergic-related network changes under propofol sedation. Further, we delineate a cognition-related reconfiguration of the dopaminergic network, highlighting the utility of REACT to explore the molecular substrates of consciousness and cognition. Academic Press 2023-05-01 /pmc/articles/PMC10410200/ /pubmed/36935083 http://dx.doi.org/10.1016/j.neuroimage.2023.120018 Text en © 2023 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lawn, Timothy
Martins, Daniel
O'Daly, Owen
Williams, Steve
Howard, Matthew
Dipasquale, Ottavia
The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening
title The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening
title_full The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening
title_fullStr The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening
title_full_unstemmed The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening
title_short The effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening
title_sort effects of propofol anaesthesia on molecular-enriched networks during resting-state and naturalistic listening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410200/
https://www.ncbi.nlm.nih.gov/pubmed/36935083
http://dx.doi.org/10.1016/j.neuroimage.2023.120018
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