Cargando…

State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states

The brainstem plays a crucial role in sleep-wake regulation. However, the ensemble dynamics underlying sleep regulation remain poorly understood. Here, we show slow, state-predictive brainstem ensemble dynamics and state-dependent interactions between the brainstem and the hippocampus in mice. On a...

Descripción completa

Detalles Bibliográficos
Autores principales: Tsunematsu, Tomomi, Patel, Amisha A, Onken, Arno, Sakata, Shuzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996931/
https://www.ncbi.nlm.nih.gov/pubmed/31934862
http://dx.doi.org/10.7554/eLife.52244
_version_ 1783493594963771392
author Tsunematsu, Tomomi
Patel, Amisha A
Onken, Arno
Sakata, Shuzo
author_facet Tsunematsu, Tomomi
Patel, Amisha A
Onken, Arno
Sakata, Shuzo
author_sort Tsunematsu, Tomomi
collection PubMed
description The brainstem plays a crucial role in sleep-wake regulation. However, the ensemble dynamics underlying sleep regulation remain poorly understood. Here, we show slow, state-predictive brainstem ensemble dynamics and state-dependent interactions between the brainstem and the hippocampus in mice. On a timescale of seconds to minutes, brainstem populations can predict pupil dilation and vigilance states and exhibit longer prediction power than hippocampal CA1 neurons. On a timescale of sub-seconds, pontine waves (P-waves) are accompanied by synchronous firing of brainstem neurons during both rapid eye movement (REM) and non-REM (NREM) sleep. Crucially, P-waves functionally interact with CA1 activity in a state-dependent manner: during NREM sleep, hippocampal sharp wave-ripples (SWRs) precede P-waves. On the other hand, P-waves during REM sleep are phase-locked with ongoing theta oscillations and are followed by burst firing of CA1 neurons. This state-dependent global coordination between the brainstem and hippocampus implicates distinct functional roles of sleep.
format Online
Article
Text
id pubmed-6996931
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-69969312020-02-05 State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states Tsunematsu, Tomomi Patel, Amisha A Onken, Arno Sakata, Shuzo eLife Neuroscience The brainstem plays a crucial role in sleep-wake regulation. However, the ensemble dynamics underlying sleep regulation remain poorly understood. Here, we show slow, state-predictive brainstem ensemble dynamics and state-dependent interactions between the brainstem and the hippocampus in mice. On a timescale of seconds to minutes, brainstem populations can predict pupil dilation and vigilance states and exhibit longer prediction power than hippocampal CA1 neurons. On a timescale of sub-seconds, pontine waves (P-waves) are accompanied by synchronous firing of brainstem neurons during both rapid eye movement (REM) and non-REM (NREM) sleep. Crucially, P-waves functionally interact with CA1 activity in a state-dependent manner: during NREM sleep, hippocampal sharp wave-ripples (SWRs) precede P-waves. On the other hand, P-waves during REM sleep are phase-locked with ongoing theta oscillations and are followed by burst firing of CA1 neurons. This state-dependent global coordination between the brainstem and hippocampus implicates distinct functional roles of sleep. eLife Sciences Publications, Ltd 2020-01-14 /pmc/articles/PMC6996931/ /pubmed/31934862 http://dx.doi.org/10.7554/eLife.52244 Text en © 2020, Tsunematsu et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Tsunematsu, Tomomi
Patel, Amisha A
Onken, Arno
Sakata, Shuzo
State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states
title State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states
title_full State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states
title_fullStr State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states
title_full_unstemmed State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states
title_short State-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states
title_sort state-dependent brainstem ensemble dynamics and their interactions with hippocampus across sleep states
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996931/
https://www.ncbi.nlm.nih.gov/pubmed/31934862
http://dx.doi.org/10.7554/eLife.52244
work_keys_str_mv AT tsunematsutomomi statedependentbrainstemensembledynamicsandtheirinteractionswithhippocampusacrosssleepstates
AT patelamishaa statedependentbrainstemensembledynamicsandtheirinteractionswithhippocampusacrosssleepstates
AT onkenarno statedependentbrainstemensembledynamicsandtheirinteractionswithhippocampusacrosssleepstates
AT sakatashuzo statedependentbrainstemensembledynamicsandtheirinteractionswithhippocampusacrosssleepstates