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Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure

We tested the hypothesis during the combined challenges of altered inspired O(2) fraction (F(I)O(2)) and posture changes at lower power output regardless of body position that the vascular conductance (VC) recruitment to the exercising muscle would not limit muscle perfusion and estimated O(2) deliv...

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Autores principales: Villar, Rodrigo, Hughson, Richard L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350166/
https://www.ncbi.nlm.nih.gov/pubmed/28292884
http://dx.doi.org/10.14814/phy2.13144
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author Villar, Rodrigo
Hughson, Richard L.
author_facet Villar, Rodrigo
Hughson, Richard L.
author_sort Villar, Rodrigo
collection PubMed
description We tested the hypothesis during the combined challenges of altered inspired O(2) fraction (F(I)O(2)) and posture changes at lower power output regardless of body position that the vascular conductance (VC) recruitment to the exercising muscle would not limit muscle perfusion and estimated O(2) delivery (DO(2est)). However, in head‐down tilt at the higher power output exercise in hypoxia, the recruitment of VC would have a functional limitation which would restrict muscle blood flow (MBF) leading to a limitation in DO(2est) with consequent increases in metabolic stress. Ten healthy volunteers repeated plantar flexion contractions at 20% (low power output = LPO) and 30% (higher power output = HPO) of their maximal voluntary contraction in horizontal (HOR), 35° head‐down‐tilt (HDT) and 45° head‐up‐tilt (HUT). Popliteal diameter and muscle blood flow velocity were measured by ultrasound determining MBF. VC was estimated by dividing MBF flow by MPP, and DO(2est) was estimated by MBF times saturation. LPO(HUT) in hypoxia was associated with no changes in VC and MBF leading to reduced DO(2est). In LPO(HDT) under hypoxia, despite no apparent functional limitation in the VC recruitment, rise in MBF to maintain DO(2est) was associated with marked increase in muscle electromyographic activity, indicating greater metabolic stress. In HPO(HDT) under hypoxia, a functional limitation for the recruitment of VC constrained MBF and DO(2est). Elevated muscle electromyographic signal in HPO(HDT) under hypoxia was consistent with challenged aerobic metabolisms which contributed to a greater increase in the relative stress of the exercise challenge and advance the onset of muscle fatigue.
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spelling pubmed-53501662017-03-17 Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure Villar, Rodrigo Hughson, Richard L. Physiol Rep Original Research We tested the hypothesis during the combined challenges of altered inspired O(2) fraction (F(I)O(2)) and posture changes at lower power output regardless of body position that the vascular conductance (VC) recruitment to the exercising muscle would not limit muscle perfusion and estimated O(2) delivery (DO(2est)). However, in head‐down tilt at the higher power output exercise in hypoxia, the recruitment of VC would have a functional limitation which would restrict muscle blood flow (MBF) leading to a limitation in DO(2est) with consequent increases in metabolic stress. Ten healthy volunteers repeated plantar flexion contractions at 20% (low power output = LPO) and 30% (higher power output = HPO) of their maximal voluntary contraction in horizontal (HOR), 35° head‐down‐tilt (HDT) and 45° head‐up‐tilt (HUT). Popliteal diameter and muscle blood flow velocity were measured by ultrasound determining MBF. VC was estimated by dividing MBF flow by MPP, and DO(2est) was estimated by MBF times saturation. LPO(HUT) in hypoxia was associated with no changes in VC and MBF leading to reduced DO(2est). In LPO(HDT) under hypoxia, despite no apparent functional limitation in the VC recruitment, rise in MBF to maintain DO(2est) was associated with marked increase in muscle electromyographic activity, indicating greater metabolic stress. In HPO(HDT) under hypoxia, a functional limitation for the recruitment of VC constrained MBF and DO(2est). Elevated muscle electromyographic signal in HPO(HDT) under hypoxia was consistent with challenged aerobic metabolisms which contributed to a greater increase in the relative stress of the exercise challenge and advance the onset of muscle fatigue. John Wiley and Sons Inc. 2017-03-14 /pmc/articles/PMC5350166/ /pubmed/28292884 http://dx.doi.org/10.14814/phy2.13144 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Villar, Rodrigo
Hughson, Richard L.
Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure
title Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure
title_full Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure
title_fullStr Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure
title_full_unstemmed Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure
title_short Vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure
title_sort vascular conductance and muscle blood flow during exercise are altered by inspired oxygen fraction and arterial perfusion pressure
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350166/
https://www.ncbi.nlm.nih.gov/pubmed/28292884
http://dx.doi.org/10.14814/phy2.13144
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