Cargando…

Decoding Brain Responses to Names and Voices across Different Vigilance States

Past research has demonstrated differential responses of the brain during sleep in response especially to variations in paralinguistic properties of auditory stimuli, suggesting they can still be processed “offline”. However, the nature of the underlying mechanisms remains unclear. Here, we therefor...

Descripción completa

Detalles Bibliográficos
Autores principales: Wielek, Tomasz, Blume, Christine, Wislowska, Malgorzata, del Giudice, Renata, Schabus, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152754/
https://www.ncbi.nlm.nih.gov/pubmed/34068077
http://dx.doi.org/10.3390/s21103393
_version_ 1783698661777080320
author Wielek, Tomasz
Blume, Christine
Wislowska, Malgorzata
del Giudice, Renata
Schabus, Manuel
author_facet Wielek, Tomasz
Blume, Christine
Wislowska, Malgorzata
del Giudice, Renata
Schabus, Manuel
author_sort Wielek, Tomasz
collection PubMed
description Past research has demonstrated differential responses of the brain during sleep in response especially to variations in paralinguistic properties of auditory stimuli, suggesting they can still be processed “offline”. However, the nature of the underlying mechanisms remains unclear. Here, we therefore used multivariate pattern analyses to directly test the similarities in brain activity among different sleep stages (non-rapid eye movement stages N1-N3, as well as rapid-eye movement sleep REM, and wake). We varied stimulus salience by manipulating subjective (own vs. unfamiliar name) and paralinguistic (familiar vs. unfamiliar voice) salience in 16 healthy sleepers during an 8-h sleep opportunity. Paralinguistic salience (i.e., familiar vs. unfamiliar voice) was reliably decoded from EEG response patterns during both N2 and N3 sleep. Importantly, the classifiers trained on N2 and N3 data generalized to N3 and N2, respectively, suggesting similar processing mode in these states. Moreover, projecting the classifiers’ weights using a forward model revealed similar fronto-central topographical patterns in NREM stages N2 and N3. Finally, we found no generalization from wake to any sleep stage (and vice versa) suggesting that “processing modes” or the overall processing architecture with respect to relevant oscillations and/or networks substantially change from wake to sleep. However, the results point to a single and rather uniform NREM-specific mechanism that is involved in (auditory) salience detection during sleep.
format Online
Article
Text
id pubmed-8152754
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-81527542021-05-27 Decoding Brain Responses to Names and Voices across Different Vigilance States Wielek, Tomasz Blume, Christine Wislowska, Malgorzata del Giudice, Renata Schabus, Manuel Sensors (Basel) Communication Past research has demonstrated differential responses of the brain during sleep in response especially to variations in paralinguistic properties of auditory stimuli, suggesting they can still be processed “offline”. However, the nature of the underlying mechanisms remains unclear. Here, we therefore used multivariate pattern analyses to directly test the similarities in brain activity among different sleep stages (non-rapid eye movement stages N1-N3, as well as rapid-eye movement sleep REM, and wake). We varied stimulus salience by manipulating subjective (own vs. unfamiliar name) and paralinguistic (familiar vs. unfamiliar voice) salience in 16 healthy sleepers during an 8-h sleep opportunity. Paralinguistic salience (i.e., familiar vs. unfamiliar voice) was reliably decoded from EEG response patterns during both N2 and N3 sleep. Importantly, the classifiers trained on N2 and N3 data generalized to N3 and N2, respectively, suggesting similar processing mode in these states. Moreover, projecting the classifiers’ weights using a forward model revealed similar fronto-central topographical patterns in NREM stages N2 and N3. Finally, we found no generalization from wake to any sleep stage (and vice versa) suggesting that “processing modes” or the overall processing architecture with respect to relevant oscillations and/or networks substantially change from wake to sleep. However, the results point to a single and rather uniform NREM-specific mechanism that is involved in (auditory) salience detection during sleep. MDPI 2021-05-13 /pmc/articles/PMC8152754/ /pubmed/34068077 http://dx.doi.org/10.3390/s21103393 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Wielek, Tomasz
Blume, Christine
Wislowska, Malgorzata
del Giudice, Renata
Schabus, Manuel
Decoding Brain Responses to Names and Voices across Different Vigilance States
title Decoding Brain Responses to Names and Voices across Different Vigilance States
title_full Decoding Brain Responses to Names and Voices across Different Vigilance States
title_fullStr Decoding Brain Responses to Names and Voices across Different Vigilance States
title_full_unstemmed Decoding Brain Responses to Names and Voices across Different Vigilance States
title_short Decoding Brain Responses to Names and Voices across Different Vigilance States
title_sort decoding brain responses to names and voices across different vigilance states
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152754/
https://www.ncbi.nlm.nih.gov/pubmed/34068077
http://dx.doi.org/10.3390/s21103393
work_keys_str_mv AT wielektomasz decodingbrainresponsestonamesandvoicesacrossdifferentvigilancestates
AT blumechristine decodingbrainresponsestonamesandvoicesacrossdifferentvigilancestates
AT wislowskamalgorzata decodingbrainresponsestonamesandvoicesacrossdifferentvigilancestates
AT delgiudicerenata decodingbrainresponsestonamesandvoicesacrossdifferentvigilancestates
AT schabusmanuel decodingbrainresponsestonamesandvoicesacrossdifferentvigilancestates