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Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity

Mounting evidence demonstrates that the central nervous system (CNS) orchestrates glucose homeostasis by sensing glucose and modulating peripheral metabolism. Glucose responsive neuronal populations have been identified in the hypothalamus and several corticolimbic regions. However, how these CNS gl...

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Autores principales: Huang, Yuhao, Wang, Jeffrey B., Parker, Jonathon J., Shivacharan, Rajat, Lal, Rayhan A., Halpern, Casey H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174612/
https://www.ncbi.nlm.nih.gov/pubmed/37169738
http://dx.doi.org/10.1038/s41467-023-38253-7
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author Huang, Yuhao
Wang, Jeffrey B.
Parker, Jonathon J.
Shivacharan, Rajat
Lal, Rayhan A.
Halpern, Casey H.
author_facet Huang, Yuhao
Wang, Jeffrey B.
Parker, Jonathon J.
Shivacharan, Rajat
Lal, Rayhan A.
Halpern, Casey H.
author_sort Huang, Yuhao
collection PubMed
description Mounting evidence demonstrates that the central nervous system (CNS) orchestrates glucose homeostasis by sensing glucose and modulating peripheral metabolism. Glucose responsive neuronal populations have been identified in the hypothalamus and several corticolimbic regions. However, how these CNS gluco-regulatory regions modulate peripheral glucose levels is not well understood. To better understand this process, we simultaneously measured interstitial glucose concentrations and local field potentials in 3 human subjects from cortical and subcortical regions, including the hypothalamus in one subject. Correlations between high frequency activity (HFA, 70–170 Hz) and peripheral glucose levels are found across multiple brain regions, notably in the hypothalamus, with correlation magnitude modulated by sleep-wake cycles, circadian coupling, and hypothalamic connectivity. Correlations are further present between non-circadian (ultradian) HFA and glucose levels which are higher during awake periods. Spectro-spatial features of neural activity enable decoding of peripheral glucose levels both in the present and up to hours in the future. Our findings demonstrate proactive encoding of homeostatic glucose dynamics by the CNS.
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spelling pubmed-101746122023-05-13 Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity Huang, Yuhao Wang, Jeffrey B. Parker, Jonathon J. Shivacharan, Rajat Lal, Rayhan A. Halpern, Casey H. Nat Commun Article Mounting evidence demonstrates that the central nervous system (CNS) orchestrates glucose homeostasis by sensing glucose and modulating peripheral metabolism. Glucose responsive neuronal populations have been identified in the hypothalamus and several corticolimbic regions. However, how these CNS gluco-regulatory regions modulate peripheral glucose levels is not well understood. To better understand this process, we simultaneously measured interstitial glucose concentrations and local field potentials in 3 human subjects from cortical and subcortical regions, including the hypothalamus in one subject. Correlations between high frequency activity (HFA, 70–170 Hz) and peripheral glucose levels are found across multiple brain regions, notably in the hypothalamus, with correlation magnitude modulated by sleep-wake cycles, circadian coupling, and hypothalamic connectivity. Correlations are further present between non-circadian (ultradian) HFA and glucose levels which are higher during awake periods. Spectro-spatial features of neural activity enable decoding of peripheral glucose levels both in the present and up to hours in the future. Our findings demonstrate proactive encoding of homeostatic glucose dynamics by the CNS. Nature Publishing Group UK 2023-05-11 /pmc/articles/PMC10174612/ /pubmed/37169738 http://dx.doi.org/10.1038/s41467-023-38253-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huang, Yuhao
Wang, Jeffrey B.
Parker, Jonathon J.
Shivacharan, Rajat
Lal, Rayhan A.
Halpern, Casey H.
Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity
title Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity
title_full Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity
title_fullStr Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity
title_full_unstemmed Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity
title_short Spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity
title_sort spectro-spatial features in distributed human intracranial activity proactively encode peripheral metabolic activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174612/
https://www.ncbi.nlm.nih.gov/pubmed/37169738
http://dx.doi.org/10.1038/s41467-023-38253-7
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