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Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice

In the adult sensory cortex, increases in neural activity elicited by sensory stimulation usually drive vasodilation mediated by neurovascular coupling. However, whether neurovascular coupling is the same in neonatal animals as adults is controversial, as both canonical and inverted responses have b...

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Autores principales: Gheres, Kyle W., Ünsal, Hayreddin S., Han, Xu, Zhang, Qingguang, Turner, Kevin L., Zhang, Nanyin, Drew, Patrick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352318/
https://www.ncbi.nlm.nih.gov/pubmed/37460780
http://dx.doi.org/10.1038/s42003-023-05121-5
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author Gheres, Kyle W.
Ünsal, Hayreddin S.
Han, Xu
Zhang, Qingguang
Turner, Kevin L.
Zhang, Nanyin
Drew, Patrick J.
author_facet Gheres, Kyle W.
Ünsal, Hayreddin S.
Han, Xu
Zhang, Qingguang
Turner, Kevin L.
Zhang, Nanyin
Drew, Patrick J.
author_sort Gheres, Kyle W.
collection PubMed
description In the adult sensory cortex, increases in neural activity elicited by sensory stimulation usually drive vasodilation mediated by neurovascular coupling. However, whether neurovascular coupling is the same in neonatal animals as adults is controversial, as both canonical and inverted responses have been observed. We investigated the nature of neurovascular coupling in unanesthetized neonatal mice using optical imaging, electrophysiology, and BOLD fMRI. We find in neonatal (postnatal day 15, P15) mice, sensory stimulation induces a small increase in blood volume/BOLD signal, often followed by a large decrease in blood volume. An examination of arousal state of the mice revealed that neonatal mice were asleep a substantial fraction of the time, and that stimulation caused the animal to awaken. As cortical blood volume is much higher during REM and NREM sleep than the awake state, awakening occludes any sensory-evoked neurovascular coupling. When neonatal mice are stimulated during an awake period, they showed relatively normal (but slowed) neurovascular coupling, showing that that the typically observed constriction is due to arousal state changes. These result show that sleep-related vascular changes dominate over any sensory-evoked changes, and hemodynamic measures need to be considered in the context of arousal state changes.
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spelling pubmed-103523182023-07-19 Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice Gheres, Kyle W. Ünsal, Hayreddin S. Han, Xu Zhang, Qingguang Turner, Kevin L. Zhang, Nanyin Drew, Patrick J. Commun Biol Article In the adult sensory cortex, increases in neural activity elicited by sensory stimulation usually drive vasodilation mediated by neurovascular coupling. However, whether neurovascular coupling is the same in neonatal animals as adults is controversial, as both canonical and inverted responses have been observed. We investigated the nature of neurovascular coupling in unanesthetized neonatal mice using optical imaging, electrophysiology, and BOLD fMRI. We find in neonatal (postnatal day 15, P15) mice, sensory stimulation induces a small increase in blood volume/BOLD signal, often followed by a large decrease in blood volume. An examination of arousal state of the mice revealed that neonatal mice were asleep a substantial fraction of the time, and that stimulation caused the animal to awaken. As cortical blood volume is much higher during REM and NREM sleep than the awake state, awakening occludes any sensory-evoked neurovascular coupling. When neonatal mice are stimulated during an awake period, they showed relatively normal (but slowed) neurovascular coupling, showing that that the typically observed constriction is due to arousal state changes. These result show that sleep-related vascular changes dominate over any sensory-evoked changes, and hemodynamic measures need to be considered in the context of arousal state changes. Nature Publishing Group UK 2023-07-17 /pmc/articles/PMC10352318/ /pubmed/37460780 http://dx.doi.org/10.1038/s42003-023-05121-5 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
Gheres, Kyle W.
Ünsal, Hayreddin S.
Han, Xu
Zhang, Qingguang
Turner, Kevin L.
Zhang, Nanyin
Drew, Patrick J.
Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice
title Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice
title_full Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice
title_fullStr Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice
title_full_unstemmed Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice
title_short Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice
title_sort arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352318/
https://www.ncbi.nlm.nih.gov/pubmed/37460780
http://dx.doi.org/10.1038/s42003-023-05121-5
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