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Global Reach 2018: Nitric oxide-mediated cutaneous vasodilation is reduced in chronic, but not acute, hypoxia independently of enzymatic superoxide formation. / Coombs, Geoff B; Akins, John D; Patik, Jordan C et al.
Yn: Free radical biology & medicine, Cyfrol 172, 20.08.2021, t. 451-458.

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HarvardHarvard

Coombs, GB, Akins, JD, Patik, JC, Vizcardo-Galindo, GA, Figueroa-Mujica, R, Tymko, MM, Stacey, BS, Iannetelli, A, Bailey, DM, Villafuerte, FC, Ainslie, PN & Brothers, RM 2021, 'Global Reach 2018: Nitric oxide-mediated cutaneous vasodilation is reduced in chronic, but not acute, hypoxia independently of enzymatic superoxide formation', Free radical biology & medicine, cyfrol. 172, tt. 451-458. https://doi.org/10.1016/j.freeradbiomed.2021.06.005

APA

Coombs, G. B., Akins, J. D., Patik, J. C., Vizcardo-Galindo, G. A., Figueroa-Mujica, R., Tymko, M. M., Stacey, B. S., Iannetelli, A., Bailey, D. M., Villafuerte, F. C., Ainslie, P. N., & Brothers, R. M. (2021). Global Reach 2018: Nitric oxide-mediated cutaneous vasodilation is reduced in chronic, but not acute, hypoxia independently of enzymatic superoxide formation. Free radical biology & medicine, 172, 451-458. https://doi.org/10.1016/j.freeradbiomed.2021.06.005

CBE

Coombs GB, Akins JD, Patik JC, Vizcardo-Galindo GA, Figueroa-Mujica R, Tymko MM, Stacey BS, Iannetelli A, Bailey DM, Villafuerte FC, et al. 2021. Global Reach 2018: Nitric oxide-mediated cutaneous vasodilation is reduced in chronic, but not acute, hypoxia independently of enzymatic superoxide formation. Free radical biology & medicine. 172:451-458. https://doi.org/10.1016/j.freeradbiomed.2021.06.005

MLA

VancouverVancouver

Coombs GB, Akins JD, Patik JC, Vizcardo-Galindo GA, Figueroa-Mujica R, Tymko MM et al. Global Reach 2018: Nitric oxide-mediated cutaneous vasodilation is reduced in chronic, but not acute, hypoxia independently of enzymatic superoxide formation. Free radical biology & medicine. 2021 Awst 20;172:451-458. doi: 10.1016/j.freeradbiomed.2021.06.005

Author

RIS

TY - JOUR

T1 - Global Reach 2018

T2 - Nitric oxide-mediated cutaneous vasodilation is reduced in chronic, but not acute, hypoxia independently of enzymatic superoxide formation

AU - Coombs, Geoff B

AU - Akins, John D

AU - Patik, Jordan C

AU - Vizcardo-Galindo, Gustavo A

AU - Figueroa-Mujica, Romulo

AU - Tymko, Michael M

AU - Stacey, Benjamin S

AU - Iannetelli, Angelo

AU - Bailey, Damian M

AU - Villafuerte, Francisco C

AU - Ainslie, Philip N

AU - Brothers, R Matthew

N1 - Copyright © 2021 Elsevier Inc. All rights reserved.

PY - 2021/8/20

Y1 - 2021/8/20

N2 - We tested the hypotheses that 1) cutaneous microvascular function is impaired by acute normobaric and chronic hypobaric hypoxia and 2) that the superoxide free radical (via NADPH oxidase or xanthine oxidase) contributes to this impairment via nitric oxide (NO) scavenging. Local heating-induced cutaneous hyperemia (39 °C) was measured in the forearm of 11 male lowlanders at sea level (SL) and following 14-18 days at high altitude (HA; 4340 m in Cerro de Pasco, Peru), and compared to 11 highlanders residing permanently at this elevation. Cutaneous vascular conductance (CVC; laser-Doppler flux/mean arterial pressure) was not different during 39 °C [control site: 73 (19) vs. 71 (18)%max; P = 0.68] between normoxia and acute normobaric hypoxia (FIO2 = 0.125; equivalent to HA), respectively. At HA, CVC was reduced during 39 °C in lowlanders compared to SL [control site: 54 (14) vs. 73 (19)%max; P < 0.01] and was lower in Andean highlanders compared to lowlanders at HA [control site: 50 (24) vs. 54 (14)%max; P = 0.02]. The NO contribution to vasodilation during 39 °C (i.e., effect of NO synthase inhibition) was reduced in lowlanders at HA compared to SL [control site: 41 (11) vs 49 (10)%max; P = 0.04] and in Andean highlanders compared to lowlanders at HA [control site: 32 (21) vs. 41 (11)%max; P = 0.01]. Intradermal administration (cutaneous microdialysis) of the superoxide mimetic Tempol, inhibition of xanthine oxidase (via allopurinol), or NADPH oxidase (via apocynin) had no influence on cutaneous endothelium-dependent dilation during any of the conditions (all main effects of drug P > 0.05). These results suggest that time at HA impairs NO-mediated cutaneous vasodilation independent of enzymatic superoxide formation.

AB - We tested the hypotheses that 1) cutaneous microvascular function is impaired by acute normobaric and chronic hypobaric hypoxia and 2) that the superoxide free radical (via NADPH oxidase or xanthine oxidase) contributes to this impairment via nitric oxide (NO) scavenging. Local heating-induced cutaneous hyperemia (39 °C) was measured in the forearm of 11 male lowlanders at sea level (SL) and following 14-18 days at high altitude (HA; 4340 m in Cerro de Pasco, Peru), and compared to 11 highlanders residing permanently at this elevation. Cutaneous vascular conductance (CVC; laser-Doppler flux/mean arterial pressure) was not different during 39 °C [control site: 73 (19) vs. 71 (18)%max; P = 0.68] between normoxia and acute normobaric hypoxia (FIO2 = 0.125; equivalent to HA), respectively. At HA, CVC was reduced during 39 °C in lowlanders compared to SL [control site: 54 (14) vs. 73 (19)%max; P < 0.01] and was lower in Andean highlanders compared to lowlanders at HA [control site: 50 (24) vs. 54 (14)%max; P = 0.02]. The NO contribution to vasodilation during 39 °C (i.e., effect of NO synthase inhibition) was reduced in lowlanders at HA compared to SL [control site: 41 (11) vs 49 (10)%max; P = 0.04] and in Andean highlanders compared to lowlanders at HA [control site: 32 (21) vs. 41 (11)%max; P = 0.01]. Intradermal administration (cutaneous microdialysis) of the superoxide mimetic Tempol, inhibition of xanthine oxidase (via allopurinol), or NADPH oxidase (via apocynin) had no influence on cutaneous endothelium-dependent dilation during any of the conditions (all main effects of drug P > 0.05). These results suggest that time at HA impairs NO-mediated cutaneous vasodilation independent of enzymatic superoxide formation.

KW - Humans

KW - Hypoxia

KW - Male

KW - Nitric Oxide

KW - Regional Blood Flow

KW - Skin

KW - Superoxides

KW - Vasodilation

U2 - 10.1016/j.freeradbiomed.2021.06.005

DO - 10.1016/j.freeradbiomed.2021.06.005

M3 - Article

C2 - 34129928

VL - 172

SP - 451

EP - 458

JO - Free radical biology & medicine

JF - Free radical biology & medicine

SN - 0891-5849

ER -