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Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats
Slow waves and cognitive output have been modulated in humans by phase-targeted auditory stimulation. However, to advance its technical development and further our understanding, implementation of the method in animal models is indispensable. Here, we report the successful employment of slow waves’...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530509/ https://www.ncbi.nlm.nih.gov/pubmed/34612204 http://dx.doi.org/10.7554/eLife.68043 |
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author | Moreira, Carlos G Baumann, Christian R Scandella, Maurizio Nemirovsky, Sergio I Leach, Sven Huber, Reto Noain, Daniela |
author_facet | Moreira, Carlos G Baumann, Christian R Scandella, Maurizio Nemirovsky, Sergio I Leach, Sven Huber, Reto Noain, Daniela |
author_sort | Moreira, Carlos G |
collection | PubMed |
description | Slow waves and cognitive output have been modulated in humans by phase-targeted auditory stimulation. However, to advance its technical development and further our understanding, implementation of the method in animal models is indispensable. Here, we report the successful employment of slow waves’ phase-targeted closed-loop auditory stimulation (CLAS) in rats. To validate this new tool both conceptually and functionally, we tested the effects of up- and down-phase CLAS on proportions and spectral characteristics of sleep, and on learning performance in the single-pellet reaching task, respectively. Without affecting 24 hr sleep-wake behavior, CLAS specifically altered delta (slow waves) and sigma (sleep spindles) power persistently over chronic periods of stimulation. While up-phase CLAS does not elicit a significant change in behavioral performance, down-phase CLAS exerted a detrimental effect on overall engagement and success rate in the behavioral test. Overall CLAS-dependent spectral changes were positively correlated with learning performance. Altogether, our results provide proof-of-principle evidence that phase-targeted CLAS of slow waves in rodents is efficient, safe, and stable over chronic experimental periods, enabling the use of this high-specificity tool for basic and preclinical translational sleep research. |
format | Online Article Text |
id | pubmed-8530509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-85305092021-10-25 Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats Moreira, Carlos G Baumann, Christian R Scandella, Maurizio Nemirovsky, Sergio I Leach, Sven Huber, Reto Noain, Daniela eLife Neuroscience Slow waves and cognitive output have been modulated in humans by phase-targeted auditory stimulation. However, to advance its technical development and further our understanding, implementation of the method in animal models is indispensable. Here, we report the successful employment of slow waves’ phase-targeted closed-loop auditory stimulation (CLAS) in rats. To validate this new tool both conceptually and functionally, we tested the effects of up- and down-phase CLAS on proportions and spectral characteristics of sleep, and on learning performance in the single-pellet reaching task, respectively. Without affecting 24 hr sleep-wake behavior, CLAS specifically altered delta (slow waves) and sigma (sleep spindles) power persistently over chronic periods of stimulation. While up-phase CLAS does not elicit a significant change in behavioral performance, down-phase CLAS exerted a detrimental effect on overall engagement and success rate in the behavioral test. Overall CLAS-dependent spectral changes were positively correlated with learning performance. Altogether, our results provide proof-of-principle evidence that phase-targeted CLAS of slow waves in rodents is efficient, safe, and stable over chronic experimental periods, enabling the use of this high-specificity tool for basic and preclinical translational sleep research. eLife Sciences Publications, Ltd 2021-10-06 /pmc/articles/PMC8530509/ /pubmed/34612204 http://dx.doi.org/10.7554/eLife.68043 Text en © 2021, Moreira et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Moreira, Carlos G Baumann, Christian R Scandella, Maurizio Nemirovsky, Sergio I Leach, Sven Huber, Reto Noain, Daniela Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats |
title | Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats |
title_full | Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats |
title_fullStr | Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats |
title_full_unstemmed | Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats |
title_short | Closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats |
title_sort | closed-loop auditory stimulation method to modulate sleep slow waves and motor learning performance in rats |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530509/ https://www.ncbi.nlm.nih.gov/pubmed/34612204 http://dx.doi.org/10.7554/eLife.68043 |
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