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

Abstract 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 (SWR...

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Main Authors: Yu Liu, Samuel S. McAfee, Detlef H. Heck
Format: Article
Language:English
Published: Nature Publishing Group 2017-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-09511-8
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spelling doaj-0e5661aaeff947f8a90f1ea8f84edcd52020-12-08T02:11:31ZengNature Publishing GroupScientific Reports2045-23222017-08-01711910.1038/s41598-017-09511-8Hippocampal sharp-wave ripples in awake mice are entrained by respirationYu Liu0Samuel S. McAfee1Detlef H. Heck2Department of Anatomy and Neurobiology, University of Tennessee HSCDepartment of Anatomy and Neurobiology, University of Tennessee HSCDepartment of Anatomy and Neurobiology, University of Tennessee HSCAbstract 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.https://doi.org/10.1038/s41598-017-09511-8
collection DOAJ
language English
format Article
sources DOAJ
author Yu Liu
Samuel S. McAfee
Detlef H. Heck
spellingShingle Yu Liu
Samuel S. McAfee
Detlef H. Heck
Hippocampal sharp-wave ripples in awake mice are entrained by respiration
Scientific Reports
author_facet Yu Liu
Samuel S. McAfee
Detlef H. Heck
author_sort Yu Liu
title 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_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_sort hippocampal sharp-wave ripples in awake mice are entrained by respiration
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-08-01
description Abstract 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.
url https://doi.org/10.1038/s41598-017-09511-8
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AT samuelsmcafee hippocampalsharpwaveripplesinawakemiceareentrainedbyrespiration
AT detlefhheck hippocampalsharpwaveripplesinawakemiceareentrainedbyrespiration
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