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Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain

Slow brain oscillations are usually coherent over long distances and thought to link distributed cell assemblies. In mice, theta (5–10 Hz) stands as one of the most studied slow rhythms. However, mice often breathe at theta frequency, and we recently reported that nasal respiration leads to local fi...

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Autores principales: Tort, Adriano B. L., Ponsel, Simon, Jessberger, Jakob, Yanovsky, Yevgenij, Brankačk, Jurij, Draguhn, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915406/
https://www.ncbi.nlm.nih.gov/pubmed/29691421
http://dx.doi.org/10.1038/s41598-018-24629-z
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author Tort, Adriano B. L.
Ponsel, Simon
Jessberger, Jakob
Yanovsky, Yevgenij
Brankačk, Jurij
Draguhn, Andreas
author_facet Tort, Adriano B. L.
Ponsel, Simon
Jessberger, Jakob
Yanovsky, Yevgenij
Brankačk, Jurij
Draguhn, Andreas
author_sort Tort, Adriano B. L.
collection PubMed
description Slow brain oscillations are usually coherent over long distances and thought to link distributed cell assemblies. In mice, theta (5–10 Hz) stands as one of the most studied slow rhythms. However, mice often breathe at theta frequency, and we recently reported that nasal respiration leads to local field potential (LFP) oscillations that are independent of theta. Namely, we showed respiration-coupled oscillations in the hippocampus, prelimbic cortex, and parietal cortex, suggesting that respiration could impose a global brain rhythm. Here we extend these findings by analyzing LFPs from 15 brain regions recorded simultaneously with respiration during exploration and REM sleep. We find that respiration-coupled oscillations can be detected in parallel with theta in several neocortical regions, from prefrontal to visual areas, and also in subcortical structures such as the thalamus, amygdala and ventral hippocampus. They might have escaped attention in previous studies due to the absence of respiration monitoring, the similarity with theta oscillations, and the highly variable peak frequency. We hypothesize that respiration-coupled oscillations constitute a global brain rhythm suited to entrain distributed networks into a common regime. However, whether their widespread presence reflects local network activity or is due to volume conduction remains to be determined.
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spelling pubmed-59154062018-04-30 Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain Tort, Adriano B. L. Ponsel, Simon Jessberger, Jakob Yanovsky, Yevgenij Brankačk, Jurij Draguhn, Andreas Sci Rep Article Slow brain oscillations are usually coherent over long distances and thought to link distributed cell assemblies. In mice, theta (5–10 Hz) stands as one of the most studied slow rhythms. However, mice often breathe at theta frequency, and we recently reported that nasal respiration leads to local field potential (LFP) oscillations that are independent of theta. Namely, we showed respiration-coupled oscillations in the hippocampus, prelimbic cortex, and parietal cortex, suggesting that respiration could impose a global brain rhythm. Here we extend these findings by analyzing LFPs from 15 brain regions recorded simultaneously with respiration during exploration and REM sleep. We find that respiration-coupled oscillations can be detected in parallel with theta in several neocortical regions, from prefrontal to visual areas, and also in subcortical structures such as the thalamus, amygdala and ventral hippocampus. They might have escaped attention in previous studies due to the absence of respiration monitoring, the similarity with theta oscillations, and the highly variable peak frequency. We hypothesize that respiration-coupled oscillations constitute a global brain rhythm suited to entrain distributed networks into a common regime. However, whether their widespread presence reflects local network activity or is due to volume conduction remains to be determined. Nature Publishing Group UK 2018-04-24 /pmc/articles/PMC5915406/ /pubmed/29691421 http://dx.doi.org/10.1038/s41598-018-24629-z Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tort, Adriano B. L.
Ponsel, Simon
Jessberger, Jakob
Yanovsky, Yevgenij
Brankačk, Jurij
Draguhn, Andreas
Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
title Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
title_full Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
title_fullStr Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
title_full_unstemmed Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
title_short Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
title_sort parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915406/
https://www.ncbi.nlm.nih.gov/pubmed/29691421
http://dx.doi.org/10.1038/s41598-018-24629-z
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