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Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice

Non-invasive stimulation technologies are emerging as potential treatment options for a range of neurodegenerative disorders. Experimental evidence suggests that stimuli-evoked changes in slow brain rhythms may mitigate or even prevent neuropathological and behavioral impairments. Slow wave activity...

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Autores principales: Thankachan, Stephen, Yang, Chun, Kastanenka, Ksenia V., Bacskai, Brian J., Gerashchenko, Dmitry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296645/
https://www.ncbi.nlm.nih.gov/pubmed/35853986
http://dx.doi.org/10.1038/s41598-022-16478-8
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author Thankachan, Stephen
Yang, Chun
Kastanenka, Ksenia V.
Bacskai, Brian J.
Gerashchenko, Dmitry
author_facet Thankachan, Stephen
Yang, Chun
Kastanenka, Ksenia V.
Bacskai, Brian J.
Gerashchenko, Dmitry
author_sort Thankachan, Stephen
collection PubMed
description Non-invasive stimulation technologies are emerging as potential treatment options for a range of neurodegenerative disorders. Experimental evidence suggests that stimuli-evoked changes in slow brain rhythms may mitigate or even prevent neuropathological and behavioral impairments. Slow wave activity is prevalent during sleep and can be triggered non-invasively by sensory stimulation targeting the visual system or directly via activation of neurons locally using optogenetics. Here, we developed new tools for delivering visual stimulation using light-emitting diodes in freely moving mice while awake and during sleep. We compared these tools to traditional optogenetic approaches used for local stimulation of neurons in the cerebral cortex. We then used these tools to compare the effects of low-frequency visual versus optogenetic stimulations on the slow wave activity and sleep pattern in mice. Visual stimulation effectively enhanced slow wave activity without disrupting the sleep pattern. Optogenetic stimulation of cortical GABAergic neurons increased NREM sleep. These results suggest that visual stimulation can be effective at boosting slow wave activity without having adverse effects on sleep and thus holds great potential as a non-invasive stimulation treatment strategy.
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spelling pubmed-92966452022-07-21 Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice Thankachan, Stephen Yang, Chun Kastanenka, Ksenia V. Bacskai, Brian J. Gerashchenko, Dmitry Sci Rep Article Non-invasive stimulation technologies are emerging as potential treatment options for a range of neurodegenerative disorders. Experimental evidence suggests that stimuli-evoked changes in slow brain rhythms may mitigate or even prevent neuropathological and behavioral impairments. Slow wave activity is prevalent during sleep and can be triggered non-invasively by sensory stimulation targeting the visual system or directly via activation of neurons locally using optogenetics. Here, we developed new tools for delivering visual stimulation using light-emitting diodes in freely moving mice while awake and during sleep. We compared these tools to traditional optogenetic approaches used for local stimulation of neurons in the cerebral cortex. We then used these tools to compare the effects of low-frequency visual versus optogenetic stimulations on the slow wave activity and sleep pattern in mice. Visual stimulation effectively enhanced slow wave activity without disrupting the sleep pattern. Optogenetic stimulation of cortical GABAergic neurons increased NREM sleep. These results suggest that visual stimulation can be effective at boosting slow wave activity without having adverse effects on sleep and thus holds great potential as a non-invasive stimulation treatment strategy. Nature Publishing Group UK 2022-07-19 /pmc/articles/PMC9296645/ /pubmed/35853986 http://dx.doi.org/10.1038/s41598-022-16478-8 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
Thankachan, Stephen
Yang, Chun
Kastanenka, Ksenia V.
Bacskai, Brian J.
Gerashchenko, Dmitry
Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice
title Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice
title_full Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice
title_fullStr Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice
title_full_unstemmed Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice
title_short Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice
title_sort low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296645/
https://www.ncbi.nlm.nih.gov/pubmed/35853986
http://dx.doi.org/10.1038/s41598-022-16478-8
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