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Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo

Neurovascular coupling (NVC) is a mechanism that, amongst other known and latent critical functions, ensures activated brain regions are adequately supplied with oxygen and glucose. This biological phenomenon underpins non-invasive perfusion-related neuroimaging techniques and recent reports have im...

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Autores principales: Boorman, Luke W., Harris, Samuel S., Shabir, Osman, Lee, Llywelyn, Eyre, Beth, Howarth, Clare, Berwick, Jason
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935519/
https://www.ncbi.nlm.nih.gov/pubmed/36797344
http://dx.doi.org/10.1038/s42003-023-04542-6
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author Boorman, Luke W.
Harris, Samuel S.
Shabir, Osman
Lee, Llywelyn
Eyre, Beth
Howarth, Clare
Berwick, Jason
author_facet Boorman, Luke W.
Harris, Samuel S.
Shabir, Osman
Lee, Llywelyn
Eyre, Beth
Howarth, Clare
Berwick, Jason
author_sort Boorman, Luke W.
collection PubMed
description Neurovascular coupling (NVC) is a mechanism that, amongst other known and latent critical functions, ensures activated brain regions are adequately supplied with oxygen and glucose. This biological phenomenon underpins non-invasive perfusion-related neuroimaging techniques and recent reports have implicated NVC impairment in several neurodegenerative disorders. Yet, much remains unknown regarding NVC in health and disease, and only recently has there been burgeoning recognition of a close interplay with brain thermodynamics. Accordingly, we developed a novel multi-modal approach to systematically modulate cortical temperature and interrogate the spatiotemporal dynamics of sensory-evoked NVC. We show that changes in cortical temperature profoundly and intricately modulate NVC, with low temperatures associated with diminished oxygen delivery, and high temperatures inducing a distinct vascular oscillation. These observations provide novel insights into the relationship between NVC and brain thermodynamics, with important implications for brain-temperature related therapies, functional biomarkers of elevated brain temperature, and in-vivo methods to study neurovascular coupling.
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spelling pubmed-99355192023-02-18 Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo Boorman, Luke W. Harris, Samuel S. Shabir, Osman Lee, Llywelyn Eyre, Beth Howarth, Clare Berwick, Jason Commun Biol Article Neurovascular coupling (NVC) is a mechanism that, amongst other known and latent critical functions, ensures activated brain regions are adequately supplied with oxygen and glucose. This biological phenomenon underpins non-invasive perfusion-related neuroimaging techniques and recent reports have implicated NVC impairment in several neurodegenerative disorders. Yet, much remains unknown regarding NVC in health and disease, and only recently has there been burgeoning recognition of a close interplay with brain thermodynamics. Accordingly, we developed a novel multi-modal approach to systematically modulate cortical temperature and interrogate the spatiotemporal dynamics of sensory-evoked NVC. We show that changes in cortical temperature profoundly and intricately modulate NVC, with low temperatures associated with diminished oxygen delivery, and high temperatures inducing a distinct vascular oscillation. These observations provide novel insights into the relationship between NVC and brain thermodynamics, with important implications for brain-temperature related therapies, functional biomarkers of elevated brain temperature, and in-vivo methods to study neurovascular coupling. Nature Publishing Group UK 2023-02-17 /pmc/articles/PMC9935519/ /pubmed/36797344 http://dx.doi.org/10.1038/s42003-023-04542-6 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
Boorman, Luke W.
Harris, Samuel S.
Shabir, Osman
Lee, Llywelyn
Eyre, Beth
Howarth, Clare
Berwick, Jason
Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo
title Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo
title_full Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo
title_fullStr Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo
title_full_unstemmed Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo
title_short Bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo
title_sort bidirectional alterations in brain temperature profoundly modulate spatiotemporal neurovascular responses in-vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935519/
https://www.ncbi.nlm.nih.gov/pubmed/36797344
http://dx.doi.org/10.1038/s42003-023-04542-6
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