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

Natsubori, A., Tsunematsu, T., Karashima, A., Imamura, H., Kabe, N., Trevisiol, A., et al. (2020). Intracellular ATP levels in mouse cortical excitatory neurons varies with sleep–wake states. Communications Biology, 3(1): 491. doi:10.1038/s42003-020-01215-6.

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 Creators:
Natsubori, A., Author
Tsunematsu, T., Author
Karashima, A., Author
Imamura, H., Author
Kabe, N., Author
Trevisiol, A.1, Author           
Hirrlinger, J.1, Author           
Kodama, T., Author
Sanagi, T., Author
Masamoto, K., Author
Takata, N., Author
Nave, K.-A.1, Author           
Matsui, K., Author
Tanaka, K.F., Author
Honda, M., Author
Affiliations:
1Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173664              

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Free keywords: Homeostasis; Sleep
 Abstract: 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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Language(s): eng - English
 Dates: 2020-09-07
 Publication Status: Published online
 Pages: 11
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1038/s42003-020-01215-6
 Degree: -

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Project name : This work was supported by a Grant for Research Fellow of the Japan Society for the Promotion of Science to A.N. (18K14756) and a Grant-in-Aids from Japan Foundation for Neuroscience and Mental Health, Narishige Neuroscience Research Foundation and Meiji Yasuda Life Foundation of Health and Welfare to A.N, PRESTO from JST (JPMJPR1887) to T.T, YoungGlia (Glial Assembly in Japan and Glial Heterogeneity in Germany) to A.N. and A.T.
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Title: Communications Biology
Source Genre: Journal
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Publ. Info: London : Springer Nature
Pages: 11 Volume / Issue: 3 (1) Sequence Number: 491 Start / End Page: - Identifier: ISSN: 2399-3642
CoNE: https://pure.mpg.de/cone/journals/resource/2399-3642