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Auditory inputs modulate intrinsic neuronal timescales during sleep

Functional magnetic resonance imaging (fMRI) studies have demonstrated that intrinsic neuronal timescales (INT) undergo modulation by external stimulation during consciousness. It remains unclear if INT keep the ability for significant stimulus-induced modulation during primary unconscious states, s...

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Autores principales: Klar, Philipp, Çatal, Yasir, Fogel, Stuart, Jocham, Gerhard, Langner, Robert, Owen, Adrian M., Northoff, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661171/
https://www.ncbi.nlm.nih.gov/pubmed/37985812
http://dx.doi.org/10.1038/s42003-023-05566-8
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author Klar, Philipp
Çatal, Yasir
Fogel, Stuart
Jocham, Gerhard
Langner, Robert
Owen, Adrian M.
Northoff, Georg
author_facet Klar, Philipp
Çatal, Yasir
Fogel, Stuart
Jocham, Gerhard
Langner, Robert
Owen, Adrian M.
Northoff, Georg
author_sort Klar, Philipp
collection PubMed
description Functional magnetic resonance imaging (fMRI) studies have demonstrated that intrinsic neuronal timescales (INT) undergo modulation by external stimulation during consciousness. It remains unclear if INT keep the ability for significant stimulus-induced modulation during primary unconscious states, such as sleep. This fMRI analysis addresses this question via a dataset that comprises an awake resting-state plus rest and stimulus states during sleep. We analyzed INT measured via temporal autocorrelation supported by median frequency (MF) in the frequency-domain. Our results were replicated using a biophysical model. There were two main findings: (1) INT prolonged while MF decreased from the awake resting-state to the N2 resting-state, and (2) INT shortened while MF increased during the auditory stimulus in sleep. The biophysical model supported these results by demonstrating prolonged INT in slowed neuronal populations that simulate the sleep resting-state compared to an awake state. Conversely, under sine wave input simulating the stimulus state during sleep, the model’s regions yielded shortened INT that returned to the awake resting-state level. Our results highlight that INT preserve reactivity to stimuli in states of unconsciousness like sleep, enhancing our understanding of unconscious brain dynamics and their reactivity to stimuli.
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spelling pubmed-106611712023-11-20 Auditory inputs modulate intrinsic neuronal timescales during sleep Klar, Philipp Çatal, Yasir Fogel, Stuart Jocham, Gerhard Langner, Robert Owen, Adrian M. Northoff, Georg Commun Biol Article Functional magnetic resonance imaging (fMRI) studies have demonstrated that intrinsic neuronal timescales (INT) undergo modulation by external stimulation during consciousness. It remains unclear if INT keep the ability for significant stimulus-induced modulation during primary unconscious states, such as sleep. This fMRI analysis addresses this question via a dataset that comprises an awake resting-state plus rest and stimulus states during sleep. We analyzed INT measured via temporal autocorrelation supported by median frequency (MF) in the frequency-domain. Our results were replicated using a biophysical model. There were two main findings: (1) INT prolonged while MF decreased from the awake resting-state to the N2 resting-state, and (2) INT shortened while MF increased during the auditory stimulus in sleep. The biophysical model supported these results by demonstrating prolonged INT in slowed neuronal populations that simulate the sleep resting-state compared to an awake state. Conversely, under sine wave input simulating the stimulus state during sleep, the model’s regions yielded shortened INT that returned to the awake resting-state level. Our results highlight that INT preserve reactivity to stimuli in states of unconsciousness like sleep, enhancing our understanding of unconscious brain dynamics and their reactivity to stimuli. Nature Publishing Group UK 2023-11-20 /pmc/articles/PMC10661171/ /pubmed/37985812 http://dx.doi.org/10.1038/s42003-023-05566-8 Text en © The Author(s) 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Klar, Philipp
Çatal, Yasir
Fogel, Stuart
Jocham, Gerhard
Langner, Robert
Owen, Adrian M.
Northoff, Georg
Auditory inputs modulate intrinsic neuronal timescales during sleep
title Auditory inputs modulate intrinsic neuronal timescales during sleep
title_full Auditory inputs modulate intrinsic neuronal timescales during sleep
title_fullStr Auditory inputs modulate intrinsic neuronal timescales during sleep
title_full_unstemmed Auditory inputs modulate intrinsic neuronal timescales during sleep
title_short Auditory inputs modulate intrinsic neuronal timescales during sleep
title_sort auditory inputs modulate intrinsic neuronal timescales during sleep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661171/
https://www.ncbi.nlm.nih.gov/pubmed/37985812
http://dx.doi.org/10.1038/s42003-023-05566-8
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