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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Nature Portfolio
2017
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oai:doaj.org-article:0e5661aaeff947f8a90f1ea8f84edcd52021-12-02T12:32:54ZHippocampal sharp-wave ripples in awake mice are entrained by respiration10.1038/s41598-017-09511-82045-2322https://doaj.org/article/0e5661aaeff947f8a90f1ea8f84edcd52017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-09511-8https://doaj.org/toc/2045-2322Abstract 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.Yu LiuSamuel S. McAfeeDetlef H. HeckNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017) |
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Medicine R Science Q Yu Liu Samuel S. McAfee Detlef H. Heck Hippocampal sharp-wave ripples in awake mice are entrained by respiration |
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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. |
format |
article |
author |
Yu Liu Samuel S. McAfee Detlef H. Heck |
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 Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/0e5661aaeff947f8a90f1ea8f84edcd5 |
work_keys_str_mv |
AT yuliu hippocampalsharpwaveripplesinawakemiceareentrainedbyrespiration AT samuelsmcafee hippocampalsharpwaveripplesinawakemiceareentrainedbyrespiration AT detlefhheck hippocampalsharpwaveripplesinawakemiceareentrainedbyrespiration |
_version_ |
1718393900627918848 |