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Hippocampal sharp-wave ripples in awake mice are entrained by respiration

Several recent studies have shown that respiration modulates oscillatory neuronal activity in the neocortex and hippocampus on a cycle-by-cycle basis. It was suggested that this respiratory influence on neuronal activity affects cognitive functions, including memory. Sharp-wave ripples (SWRs) are hi...

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Detalles Bibliográficos
Autores principales: Liu, Yu, McAfee, Samuel S., Heck, Detlef H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566471/
https://www.ncbi.nlm.nih.gov/pubmed/28827599
http://dx.doi.org/10.1038/s41598-017-09511-8
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author Liu, Yu
McAfee, Samuel S.
Heck, Detlef H.
author_facet Liu, Yu
McAfee, Samuel S.
Heck, Detlef H.
author_sort Liu, Yu
collection PubMed
description Several recent studies have shown that respiration modulates oscillatory neuronal activity in the neocortex and hippocampus on a cycle-by-cycle basis. It was suggested that this respiratory influence on neuronal activity affects cognitive functions, including memory. Sharp-wave ripples (SWRs) are high-frequency local field potential activity patterns characteristic for the hippocampus and implicated in memory consolidation and recall. Here we show that the timing of SWR events is modulated by the respiratory cycle, with a significantly increased probability of SWRs during the early expiration phase. This influence of respiration on SWR occurrence was eliminated when olfactory bulb activity was inhibited. Our findings represent a possible neuronal mechanism for a direct influence of the respiratory cycle on memory function.
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spelling pubmed-55664712017-08-23 Hippocampal sharp-wave ripples in awake mice are entrained by respiration Liu, Yu McAfee, Samuel S. Heck, Detlef H. Sci Rep Article Several recent studies have shown that respiration modulates oscillatory neuronal activity in the neocortex and hippocampus on a cycle-by-cycle basis. It was suggested that this respiratory influence on neuronal activity affects cognitive functions, including memory. Sharp-wave ripples (SWRs) are high-frequency local field potential activity patterns characteristic for the hippocampus and implicated in memory consolidation and recall. Here we show that the timing of SWR events is modulated by the respiratory cycle, with a significantly increased probability of SWRs during the early expiration phase. This influence of respiration on SWR occurrence was eliminated when olfactory bulb activity was inhibited. Our findings represent a possible neuronal mechanism for a direct influence of the respiratory cycle on memory function. Nature Publishing Group UK 2017-08-21 /pmc/articles/PMC5566471/ /pubmed/28827599 http://dx.doi.org/10.1038/s41598-017-09511-8 Text en © The Author(s) 2017 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
Liu, Yu
McAfee, Samuel S.
Heck, Detlef H.
Hippocampal sharp-wave ripples in awake mice are entrained by respiration
title Hippocampal sharp-wave ripples in awake mice are entrained by respiration
title_full Hippocampal sharp-wave ripples in awake mice are entrained by respiration
title_fullStr Hippocampal sharp-wave ripples in awake mice are entrained by respiration
title_full_unstemmed Hippocampal sharp-wave ripples in awake mice are entrained by respiration
title_short Hippocampal sharp-wave ripples in awake mice are entrained by respiration
title_sort hippocampal sharp-wave ripples in awake mice are entrained by respiration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566471/
https://www.ncbi.nlm.nih.gov/pubmed/28827599
http://dx.doi.org/10.1038/s41598-017-09511-8
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