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Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations

Objectives: We aimed to quantify the magnitude and time transients of capillary blood flow responses to acute changes in local oxygen concentration ([O(2)]), and carbon dioxide concentration ([CO(2)]) in skeletal muscle. Additionally, we sought to quantify the combined response to both low [O(2)] an...

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Autores principales: Russell McEvoy, Gaylene M., Wells, Brenda N., Kiley, Meghan E., Kaur, Kanika K., Fraser, Graham M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764012/
https://www.ncbi.nlm.nih.gov/pubmed/36561216
http://dx.doi.org/10.3389/fphys.2022.1052449
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author Russell McEvoy, Gaylene M.
Wells, Brenda N.
Kiley, Meghan E.
Kaur, Kanika K.
Fraser, Graham M.
author_facet Russell McEvoy, Gaylene M.
Wells, Brenda N.
Kiley, Meghan E.
Kaur, Kanika K.
Fraser, Graham M.
author_sort Russell McEvoy, Gaylene M.
collection PubMed
description Objectives: We aimed to quantify the magnitude and time transients of capillary blood flow responses to acute changes in local oxygen concentration ([O(2)]), and carbon dioxide concentration ([CO(2)]) in skeletal muscle. Additionally, we sought to quantify the combined response to both low [O(2)] and high [CO(2)] to mimic muscle microenvironment changes at the onset of exercise. Methods: 13 Sprague Dawley rats were anaesthetized, mechanically ventilated, and instrumented with indwelling catheters for systemic monitoring. The extensor digitorum longus muscle was blunt dissected, and reflected over a microfluidic gas exchange chamber in the stage of an inverted microscope. Four O(2) challenges, four CO(2) challenges, and a combined low O(2) (7–2%) and high CO(2) (5–10%) challenges were delivered to the surface with simultaneous visualization of capillary blood flow responses. Recordings were made for each challenge over a 1-min baseline period followed by a 2-min step change. The combined challenge employed a 1-min [O(2)] challenge followed by a 2-min change in [CO(2)]. Mean data for each sequence were fit using least-squared non-linear exponential models to determine the dynamics of each response. Results: 7–2% [O(2)] challenges decreased capillary RBC saturation within 2 s following the step change (46.53 ± 19.56% vs. 48.51 ± 19.02%, p < 0.0001, τ = 1.44 s), increased RBC velocity within 3 s (228.53 ± 190.39 μm/s vs. 235.74 ± 193.52 μm/s, p < 0.0003, τ = 35.54 s) with a 52% peak increase by the end of the challenge, hematocrit and supply rate show similar dynamics. 5–10% [CO(2)] challenges increased RBC velocity within 2 s following the step change (273.40 ± 218.06 μm/s vs. 276.75 ± 215.94 μm/s, p = 0.007, τ = 79.34s), with a 58% peak increase by the end of the challenge, supply rate and hematocrit show similar dynamics. Combined [O(2)] and [CO(2)] challenges resulted in additive responses to all microvascular hemodynamic measures with a 103% peak velocity increase by the end of the collection period. Data for mean responses and exponential fitting parameters are reported for all challenges. Conclusion: Microvascular level changes in muscle [O(2)] and [CO(2)] provoked capillary hemodynamic responses with differing time transients. Simulating exercise via combined [O(2)] and [CO(2)] challenges demonstrated the independent and additive nature of local blood flow responses to these agents.
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spelling pubmed-97640122022-12-21 Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations Russell McEvoy, Gaylene M. Wells, Brenda N. Kiley, Meghan E. Kaur, Kanika K. Fraser, Graham M. Front Physiol Physiology Objectives: We aimed to quantify the magnitude and time transients of capillary blood flow responses to acute changes in local oxygen concentration ([O(2)]), and carbon dioxide concentration ([CO(2)]) in skeletal muscle. Additionally, we sought to quantify the combined response to both low [O(2)] and high [CO(2)] to mimic muscle microenvironment changes at the onset of exercise. Methods: 13 Sprague Dawley rats were anaesthetized, mechanically ventilated, and instrumented with indwelling catheters for systemic monitoring. The extensor digitorum longus muscle was blunt dissected, and reflected over a microfluidic gas exchange chamber in the stage of an inverted microscope. Four O(2) challenges, four CO(2) challenges, and a combined low O(2) (7–2%) and high CO(2) (5–10%) challenges were delivered to the surface with simultaneous visualization of capillary blood flow responses. Recordings were made for each challenge over a 1-min baseline period followed by a 2-min step change. The combined challenge employed a 1-min [O(2)] challenge followed by a 2-min change in [CO(2)]. Mean data for each sequence were fit using least-squared non-linear exponential models to determine the dynamics of each response. Results: 7–2% [O(2)] challenges decreased capillary RBC saturation within 2 s following the step change (46.53 ± 19.56% vs. 48.51 ± 19.02%, p < 0.0001, τ = 1.44 s), increased RBC velocity within 3 s (228.53 ± 190.39 μm/s vs. 235.74 ± 193.52 μm/s, p < 0.0003, τ = 35.54 s) with a 52% peak increase by the end of the challenge, hematocrit and supply rate show similar dynamics. 5–10% [CO(2)] challenges increased RBC velocity within 2 s following the step change (273.40 ± 218.06 μm/s vs. 276.75 ± 215.94 μm/s, p = 0.007, τ = 79.34s), with a 58% peak increase by the end of the challenge, supply rate and hematocrit show similar dynamics. Combined [O(2)] and [CO(2)] challenges resulted in additive responses to all microvascular hemodynamic measures with a 103% peak velocity increase by the end of the collection period. Data for mean responses and exponential fitting parameters are reported for all challenges. Conclusion: Microvascular level changes in muscle [O(2)] and [CO(2)] provoked capillary hemodynamic responses with differing time transients. Simulating exercise via combined [O(2)] and [CO(2)] challenges demonstrated the independent and additive nature of local blood flow responses to these agents. Frontiers Media S.A. 2022-12-06 /pmc/articles/PMC9764012/ /pubmed/36561216 http://dx.doi.org/10.3389/fphys.2022.1052449 Text en Copyright © 2022 Russell McEvoy, Wells, Kiley, Kaur and Fraser. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Russell McEvoy, Gaylene M.
Wells, Brenda N.
Kiley, Meghan E.
Kaur, Kanika K.
Fraser, Graham M.
Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations
title Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations
title_full Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations
title_fullStr Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations
title_full_unstemmed Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations
title_short Dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations
title_sort dynamics of capillary blood flow responses to acute local changes in oxygen and carbon dioxide concentrations
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764012/
https://www.ncbi.nlm.nih.gov/pubmed/36561216
http://dx.doi.org/10.3389/fphys.2022.1052449
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