Acute reductions in hematocrit increase flow-mediated dilation independent ofresting nitric oxide bioavailability in humans

Gweld/ agor
Awdur
Hoiland, Ryan
Tremblay, Joshua
Stacey, Benjamin
Coombs, Geoff
Nowak-Fluck, Daniela
Tymko, Michael M.
Patrician, Alexander
Stembridge, Mike
Howe, Connor
Bailey, Damian M.
Green, Daniel
MacLeod, David
Ainslie, Philip
Dyddiad
2020-07-08Dyddiad derbyn
2020-07-02
Date Deposited
2020-07-15
Math
Article
acceptedVersion
Cyhoeddwr
Wiley
ISSN
1469-7793
Metadata
Dangos cofnod eitem llawnCrynodeb
Hemoglobin (Hb) may impact the transduction of endothelium‐dependent and nitric oxide (NO) mediated vasodilator activity, given its contribution to shear stress stimuli and diverse biochemical reactions with NO. We hypothesized that an acute reduction in [Hb] and hematocrit (Hct) would increase brachial artery flow‐mediated dilation (FMD). In eleven healthy males (28 ± 7 years; 23 ± 2 kg m−2), FMD (Duplex ultrasound), arterial blood gases, Hct and [Hb], blood viscosity, and NO metabolites (ozone‐based chemiluminescence) were measured before and after isovolumic hemodilution, where ∼20% of whole blood was removed and replaced with 5% human serum albumin. Hemodilution reduced Hct by 18 ± 2% (P < 0.001) and whole blood viscosity by 22 ± 5% (P < 0.001). Plasma nitrite (P = 0.01), S‐nitrosothiols (P = 0.03), and total red blood cell NO (P = 0.001) were collectively reduced by ∼15–40%. Brachial artery FMD increased by ∼160% from 3.8 ± 2.1 to 9.7 ± 4.5% (P = 0.004). Statistical covariation for the shear stress stimulus did not alter FMD, indicating that the increase in FMD was not directly related to alterations in whole blood viscosity and the shear stimulus. Collectively, these findings indicate that hemoglobin scavenging of NO appears to be an important factor in the regulation of FMD under normal conditions through constraint of endothelium‐dependent NO‐mediated vasodilation in healthy humans.
Cyfnodolyn/trafodion cynhadledd
Journal of Physiology;
Dyfyniad
Hoiland, R.L., Tremblay, J.C., Stacey, B.S., Coombs, G.B., Nowak‐Flück, D., Tymko, M.M., Patrician, A., Stembridge, M., Howe, C.A., Bailey, D.M. and Green, D.J. (2020) 'Acute reductions in hematocrit increase flow‐mediated dilation independent of resting nitric oxide bioavailability in humans', The Journal of Physiology.
Dynodwr Gwrthrych Digidol (DOI)
https://doi.org/10.1113/JP280141Disgrifiad
Article published in Journal of Physiology on 08 July (online), available at: https://doi.org/10.1113/JP280141.
Nawdd
Cardiff Metropolitan University (Grant ID: Cardiff Metropolian (Internal))
Canada Research Chairs (Chaires de recherche du Canada) - P. Ainslie.
Casgliadau
- Import [796]
Eitemau perthynol
Yn dangos eitemau sy’n perthyn drwy deitl, awdur, pwnc a chrynodeb.
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