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Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner

Sleep is essential but places animals at risk. Filtering acoustic information according to its relevance, a process generally known as sensory gating, is crucial during sleep to ensure a balance between rest and danger detection. The mechanisms of this sensory gating and its specificity are not unde...

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Autores principales: van Kronenberg, Philipp, Milinski, Linus, Kruschke, Zoë, de Hoz, Livia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001723/
https://www.ncbi.nlm.nih.gov/pubmed/35410339
http://dx.doi.org/10.1038/s41598-022-09457-6
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author van Kronenberg, Philipp
Milinski, Linus
Kruschke, Zoë
de Hoz, Livia
author_facet van Kronenberg, Philipp
Milinski, Linus
Kruschke, Zoë
de Hoz, Livia
author_sort van Kronenberg, Philipp
collection PubMed
description Sleep is essential but places animals at risk. Filtering acoustic information according to its relevance, a process generally known as sensory gating, is crucial during sleep to ensure a balance between rest and danger detection. The mechanisms of this sensory gating and its specificity are not understood. Here, we tested the effect that sounds of different meaning have on sleep-associated ongoing oscillations. We recorded EEG and EMG from mice during REM and NREM sleep while presenting sounds with or without behavioural relevance. We found that sound presentation per se, in the form of a neutral sound, elicited a weak or no change in the power of sleep-state-dependent EEG during REM and NREM sleep. In contrast, the presentation of a sound previously conditioned in an aversive task, elicited a clear and fast decrease in the EEG power during both sleep phases, suggesting a transition to lighter sleep without awakening. The observed changes generally weakened over training days and were not present in animals that failed to learn. Interestingly, the effect could be generalized to unfamiliar neutral sounds if presented following conditioned training, an effect that depended on sleep phase and sound type. The data demonstrate that sounds are differentially gated during sleep depending on their meaning and that this process is reflected in disruption of sleep-associated brain oscillations without behavioural arousal.
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spelling pubmed-90017232022-04-13 Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner van Kronenberg, Philipp Milinski, Linus Kruschke, Zoë de Hoz, Livia Sci Rep Article Sleep is essential but places animals at risk. Filtering acoustic information according to its relevance, a process generally known as sensory gating, is crucial during sleep to ensure a balance between rest and danger detection. The mechanisms of this sensory gating and its specificity are not understood. Here, we tested the effect that sounds of different meaning have on sleep-associated ongoing oscillations. We recorded EEG and EMG from mice during REM and NREM sleep while presenting sounds with or without behavioural relevance. We found that sound presentation per se, in the form of a neutral sound, elicited a weak or no change in the power of sleep-state-dependent EEG during REM and NREM sleep. In contrast, the presentation of a sound previously conditioned in an aversive task, elicited a clear and fast decrease in the EEG power during both sleep phases, suggesting a transition to lighter sleep without awakening. The observed changes generally weakened over training days and were not present in animals that failed to learn. Interestingly, the effect could be generalized to unfamiliar neutral sounds if presented following conditioned training, an effect that depended on sleep phase and sound type. The data demonstrate that sounds are differentially gated during sleep depending on their meaning and that this process is reflected in disruption of sleep-associated brain oscillations without behavioural arousal. Nature Publishing Group UK 2022-04-11 /pmc/articles/PMC9001723/ /pubmed/35410339 http://dx.doi.org/10.1038/s41598-022-09457-6 Text en © The Author(s) 2022 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
van Kronenberg, Philipp
Milinski, Linus
Kruschke, Zoë
de Hoz, Livia
Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner
title Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner
title_full Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner
title_fullStr Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner
title_full_unstemmed Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner
title_short Sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner
title_sort sound disrupts sleep-associated brain oscillations in rodents in a meaning-dependent manner
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001723/
https://www.ncbi.nlm.nih.gov/pubmed/35410339
http://dx.doi.org/10.1038/s41598-022-09457-6
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