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Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex

Cerebrovascular reactivity (CVR) to changes in the partial pressure of arterial carbon dioxide (PaCO(2)) is an important mechanism that maintains CO(2) or pH homeostasis in the brain. To what extent this is influenced by gravitational stress and corresponding implications for the regulation of cereb...

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Autores principales: Watanabe, Hironori, Saito, Shotaro, Washio, Takuro, Bailey, Damian Miles, Ogoh, Shigehiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770752/
https://www.ncbi.nlm.nih.gov/pubmed/35069233
http://dx.doi.org/10.3389/fphys.2021.749255
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author Watanabe, Hironori
Saito, Shotaro
Washio, Takuro
Bailey, Damian Miles
Ogoh, Shigehiko
author_facet Watanabe, Hironori
Saito, Shotaro
Washio, Takuro
Bailey, Damian Miles
Ogoh, Shigehiko
author_sort Watanabe, Hironori
collection PubMed
description Cerebrovascular reactivity (CVR) to changes in the partial pressure of arterial carbon dioxide (PaCO(2)) is an important mechanism that maintains CO(2) or pH homeostasis in the brain. To what extent this is influenced by gravitational stress and corresponding implications for the regulation of cerebral blood flow (CBF) remain unclear. The present study examined the onset responses of pulmonary ventilation (V̇(E)) and anterior middle (MCA) and posterior (PCA) cerebral artery mean blood velocity (V(mean)) responses to acute hypercapnia (5% CO(2)) to infer dynamic changes in the central respiratory chemoreflex and cerebrovascular reactivity (CVR), in supine and 50° head-up tilt (HUT) positions. Each onset response was evaluated using a single-exponential regression model consisting of the response time latency [CO(2)-response delay (t(0))] and time constant (τ). Onset response of V̇(E) and PCA V(mean) to changes in CO(2) was unchanged during 50° HUT compared with supine (τ: V̇(E), p = 0.707; PCA V(mean), p = 0.071 vs. supine) but the MCA V(mean) onset response was faster during supine than during 50° HUT (τ: p = 0.003 vs. supine). These data indicate that gravitational stress selectively impaired dynamic CVR in the anterior cerebral circulation, whereas the posterior circulation was preserved, independent of any changes to the central respiratory chemoreflex. Collectively, our findings highlight the regional heterogeneity underlying CBF regulation that may have translational implications for the microgravity (and hypercapnia) associated with deep-space flight notwithstanding terrestrial orthostatic diseases that have been linked to accelerated cognitive decline and neurodegeneration.
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spelling pubmed-87707522022-01-21 Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex Watanabe, Hironori Saito, Shotaro Washio, Takuro Bailey, Damian Miles Ogoh, Shigehiko Front Physiol Physiology Cerebrovascular reactivity (CVR) to changes in the partial pressure of arterial carbon dioxide (PaCO(2)) is an important mechanism that maintains CO(2) or pH homeostasis in the brain. To what extent this is influenced by gravitational stress and corresponding implications for the regulation of cerebral blood flow (CBF) remain unclear. The present study examined the onset responses of pulmonary ventilation (V̇(E)) and anterior middle (MCA) and posterior (PCA) cerebral artery mean blood velocity (V(mean)) responses to acute hypercapnia (5% CO(2)) to infer dynamic changes in the central respiratory chemoreflex and cerebrovascular reactivity (CVR), in supine and 50° head-up tilt (HUT) positions. Each onset response was evaluated using a single-exponential regression model consisting of the response time latency [CO(2)-response delay (t(0))] and time constant (τ). Onset response of V̇(E) and PCA V(mean) to changes in CO(2) was unchanged during 50° HUT compared with supine (τ: V̇(E), p = 0.707; PCA V(mean), p = 0.071 vs. supine) but the MCA V(mean) onset response was faster during supine than during 50° HUT (τ: p = 0.003 vs. supine). These data indicate that gravitational stress selectively impaired dynamic CVR in the anterior cerebral circulation, whereas the posterior circulation was preserved, independent of any changes to the central respiratory chemoreflex. Collectively, our findings highlight the regional heterogeneity underlying CBF regulation that may have translational implications for the microgravity (and hypercapnia) associated with deep-space flight notwithstanding terrestrial orthostatic diseases that have been linked to accelerated cognitive decline and neurodegeneration. Frontiers Media S.A. 2022-01-06 /pmc/articles/PMC8770752/ /pubmed/35069233 http://dx.doi.org/10.3389/fphys.2021.749255 Text en Copyright © 2022 Watanabe, Saito, Washio, Bailey and Ogoh. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Watanabe, Hironori
Saito, Shotaro
Washio, Takuro
Bailey, Damian Miles
Ogoh, Shigehiko
Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex
title Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex
title_full Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex
title_fullStr Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex
title_full_unstemmed Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex
title_short Acute Gravitational Stress Selectively Impairs Dynamic Cerebrovascular Reactivity in the Anterior Circulation Independent of Changes to the Central Respiratory Chemoreflex
title_sort acute gravitational stress selectively impairs dynamic cerebrovascular reactivity in the anterior circulation independent of changes to the central respiratory chemoreflex
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770752/
https://www.ncbi.nlm.nih.gov/pubmed/35069233
http://dx.doi.org/10.3389/fphys.2021.749255
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