Hemoglobin and cerebral hypoxic vasodilation in humans: evidence for nitric oxide-dependent and S-nitrosothiol mediated signal transduction

Ryan L. Hoiland*, David B. MacLeod, Benjamin Stacey, Hannah G. Caldwell, Connor A. Howe, Daniela Nowak-Flück, Jay M.R.J. Carr, Michael M. Tymko, Geoff B. Coombs, Alexander Patrician, Joshua C. Tremblay, Michelle Van Mierlo, Christopher Gasho, Michael Stembridge, Mypinder S. Sekhon, Damian Bailey, Philip Ainslie

*Awdur cyfatebol y gwaith hwn

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

14 Wedi eu Llwytho i Lawr (Pure)

Crynodeb

Cerebral hypoxic vasodilation is poorly understood in humans, which undermines the development of therapeutics to optimize cerebral oxygen delivery. Across four investigations (total n = 195) we investigated the role of nitric oxide (NO) and hemoglobin-based S-nitrosothiol (RSNO) and nitrite (NO−2) signaling in the regulation of cerebral hypoxic vasodilation. We conducted hemodilution (n = 10) and NO synthase inhibition experiments (n = 11) as well as hemoglobin oxygen desaturation protocols, wherein we measured cerebral blood flow (CBF), intra-arterial blood pressure, and in subsets of participants trans-cerebral release/uptake of RSNO and NO−2. Higher CBF during hypoxia was associated with greater trans-cerebral RSNO release but not NO−2, while NO synthase inhibition reduced cerebral hypoxic vasodilation. Hemodilution increased the magnitude of cerebral hypoxic vasodilation following acute hemodilution, while in 134 participants tested under normal conditions, hypoxic cerebral vasodilation was inversely correlated to arterial hemoglobin concentration. These studies were replicated in a sample of polycythemic high-altitude native Andeans suffering from excessive erythrocytosis (n = 40), where cerebral hypoxic vasodilation was inversely correlated to hemoglobin concentration, and improved with hemodilution (n = 6). Collectively, our data indicate that cerebral hypoxic vasodilation is partially NO-dependent, associated with trans-cerebral RSNO release, and place hemoglobin-based NO signaling as a central mechanism of cerebral hypoxic vasodilation in humans.
Iaith wreiddiolSaesneg
Tudalennau (o-i)1519-1531
Nifer y tudalennau13
CyfnodolynJournal of Cerebral Blood Flow and Metabolism
Cyfrol43
Rhif cyhoeddi9
Dyddiad ar-lein cynnar12 Ebr 2023
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - Medi 2023

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