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Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states

Whilst the brain is assumed to exert homeostatic functions to keep the cellular energy status constant under physiological conditions, this has not been experimentally proven. Here, we conducted in vivo optical recordings of intracellular concentration of adenosine 5’-triphosphate (ATP), the major c...

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Autores principales: Natsubori, Akiyo, Tsunematsu, Tomomi, Karashima, Akihiro, Imamura, Hiromi, Kabe, Naoya, Trevisiol, Andrea, Hirrlinger, Johannes, Kodama, Tohru, Sanagi, Tomomi, Masamoto, Kazuto, Takata, Norio, Nave, Klaus-Armin, Matsui, Ko, Tanaka, Kenji F., Honda, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477120/
https://www.ncbi.nlm.nih.gov/pubmed/32895482
http://dx.doi.org/10.1038/s42003-020-01215-6
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author Natsubori, Akiyo
Tsunematsu, Tomomi
Karashima, Akihiro
Imamura, Hiromi
Kabe, Naoya
Trevisiol, Andrea
Hirrlinger, Johannes
Kodama, Tohru
Sanagi, Tomomi
Masamoto, Kazuto
Takata, Norio
Nave, Klaus-Armin
Matsui, Ko
Tanaka, Kenji F.
Honda, Makoto
author_facet Natsubori, Akiyo
Tsunematsu, Tomomi
Karashima, Akihiro
Imamura, Hiromi
Kabe, Naoya
Trevisiol, Andrea
Hirrlinger, Johannes
Kodama, Tohru
Sanagi, Tomomi
Masamoto, Kazuto
Takata, Norio
Nave, Klaus-Armin
Matsui, Ko
Tanaka, Kenji F.
Honda, Makoto
author_sort Natsubori, Akiyo
collection PubMed
description Whilst the brain is assumed to exert homeostatic functions to keep the cellular energy status constant under physiological conditions, this has not been experimentally proven. Here, we conducted in vivo optical recordings of intracellular concentration of adenosine 5’-triphosphate (ATP), the major cellular energy metabolite, using a genetically encoded sensor in the mouse brain. We demonstrate that intracellular ATP levels in cortical excitatory neurons fluctuate in a cortex-wide manner depending on the sleep-wake states, correlating with arousal. Interestingly, ATP levels profoundly decreased during rapid eye movement sleep, suggesting a negative energy balance in neurons despite a simultaneous increase in cerebral hemodynamics for energy supply. The reduction in intracellular ATP was also observed in response to local electrical stimulation for neuronal activation, whereas the hemodynamics were simultaneously enhanced. These observations indicate that cerebral energy metabolism may not always meet neuronal energy demands, consequently resulting in physiological fluctuations of intracellular ATP levels in neurons.
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spelling pubmed-74771202020-09-21 Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states Natsubori, Akiyo Tsunematsu, Tomomi Karashima, Akihiro Imamura, Hiromi Kabe, Naoya Trevisiol, Andrea Hirrlinger, Johannes Kodama, Tohru Sanagi, Tomomi Masamoto, Kazuto Takata, Norio Nave, Klaus-Armin Matsui, Ko Tanaka, Kenji F. Honda, Makoto Commun Biol Article Whilst the brain is assumed to exert homeostatic functions to keep the cellular energy status constant under physiological conditions, this has not been experimentally proven. Here, we conducted in vivo optical recordings of intracellular concentration of adenosine 5’-triphosphate (ATP), the major cellular energy metabolite, using a genetically encoded sensor in the mouse brain. We demonstrate that intracellular ATP levels in cortical excitatory neurons fluctuate in a cortex-wide manner depending on the sleep-wake states, correlating with arousal. Interestingly, ATP levels profoundly decreased during rapid eye movement sleep, suggesting a negative energy balance in neurons despite a simultaneous increase in cerebral hemodynamics for energy supply. The reduction in intracellular ATP was also observed in response to local electrical stimulation for neuronal activation, whereas the hemodynamics were simultaneously enhanced. These observations indicate that cerebral energy metabolism may not always meet neuronal energy demands, consequently resulting in physiological fluctuations of intracellular ATP levels in neurons. Nature Publishing Group UK 2020-09-07 /pmc/articles/PMC7477120/ /pubmed/32895482 http://dx.doi.org/10.1038/s42003-020-01215-6 Text en © The Author(s) 2020 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
Natsubori, Akiyo
Tsunematsu, Tomomi
Karashima, Akihiro
Imamura, Hiromi
Kabe, Naoya
Trevisiol, Andrea
Hirrlinger, Johannes
Kodama, Tohru
Sanagi, Tomomi
Masamoto, Kazuto
Takata, Norio
Nave, Klaus-Armin
Matsui, Ko
Tanaka, Kenji F.
Honda, Makoto
Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states
title Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states
title_full Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states
title_fullStr Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states
title_full_unstemmed Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states
title_short Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states
title_sort intracellular atp levels in mouse cortical excitatory neurons varies with sleep–wake states
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477120/
https://www.ncbi.nlm.nih.gov/pubmed/32895482
http://dx.doi.org/10.1038/s42003-020-01215-6
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