AUTHOR=Watanabe Hironori , Saito Shotaro , Washio Takuro , Bailey Damian Miles , Ogoh Shigehiko 

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

JOURNAL=Frontiers in Physiology

VOLUME=12

YEAR=2022

URL=https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2021.749255

DOI=10.3389/fphys.2021.749255

ISSN=1664-042X

ABSTRACT=<p>Cerebrovascular reactivity (CVR) to changes in the partial pressure of arterial carbon dioxide (PaCO<sub>2</sub>) is an important mechanism that maintains CO<sub>2</sub> 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<sub>E</sub>) and anterior middle (MCA) and posterior (PCA) cerebral artery mean blood velocity (V<sub>mean</sub>) responses to acute hypercapnia (5% CO<sub>2</sub>) 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<sub>2</sub>-response delay (<italic>t</italic><sub>0</sub>)] and time constant (<italic>τ</italic>). Onset response of V̇<sub>E</sub> and PCA V<sub>mean</sub> to changes in CO<sub>2</sub> was unchanged during 50° HUT compared with supine (<italic>τ</italic>: V̇<sub>E</sub>, <italic>p</italic> = 0.707; PCA V<sub>mean</sub>, <italic>p</italic> = 0.071 vs. supine) but the MCA V<sub>mean</sub> onset response was faster during supine than during 50° HUT (<italic>τ</italic>: <italic>p</italic> = 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.</p>