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Acute changes in forearm vascular compliance during transient sympatho‐excitation

The study of vascular regulation often omits important information about the elastic properties of arteries under conditions of pulsatile flow. The purpose of this study was to examine the relationship between muscle sympathetic nerve activity (MSNA), vascular bed compliance, and peripheral blood fl...

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Autores principales: Olver, T. Dylan, Badrov, Mark B., Allen, Matti D., Coverdale, Nicole S., Shoemaker, J. Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017978/
https://www.ncbi.nlm.nih.gov/pubmed/35439367
http://dx.doi.org/10.14814/phy2.15256
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author Olver, T. Dylan
Badrov, Mark B.
Allen, Matti D.
Coverdale, Nicole S.
Shoemaker, J. Kevin
author_facet Olver, T. Dylan
Badrov, Mark B.
Allen, Matti D.
Coverdale, Nicole S.
Shoemaker, J. Kevin
author_sort Olver, T. Dylan
collection PubMed
description The study of vascular regulation often omits important information about the elastic properties of arteries under conditions of pulsatile flow. The purpose of this study was to examine the relationship between muscle sympathetic nerve activity (MSNA), vascular bed compliance, and peripheral blood flow responses in humans. We hypothesized that increases in MSNA would correlate with reductions in vascular compliance, and that changes in compliance would correspond with changes in peripheral blood flow during sympatho‐excitation. MSNA (microneurography), blood pressure (Finopres), and brachial artery blood flow (Doppler ultrasound), were monitored in six healthy males at baseline and during the last 15 s of voluntary end‐inspiratory, expiratory apneas and 5 min of static handgrip exercise (SHG; 20% maximum voluntary contraction) and 3 min of post‐exercise circulatory occlusion (SHG + PECO; measured in the non‐exercising arm). A lumped Windkessel model was employed to examine vascular bed compliance. During apnea, indices of MSNA were inversely related with vascular compliance, and reductions in compliance correlated with decreased brachial blood flow rate. During SHG, despite increased MSNA, compliance also increased, but was unrelated to increases in blood flow. Neither during SHG nor PECO did indices of MSNA correlate with forearm vascular compliance nor did vascular compliance correlate with brachial flow. However, during PECO, a linear combination of blood pressure and total MSNA was correlated with vascular compliance. These data indicate the elastic components of the forearm vasculature are regulated by adrenergic and myogenic mechanisms during sympatho‐excitation, but in a reflex‐dependent manner.
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spelling pubmed-90179782022-04-21 Acute changes in forearm vascular compliance during transient sympatho‐excitation Olver, T. Dylan Badrov, Mark B. Allen, Matti D. Coverdale, Nicole S. Shoemaker, J. Kevin Physiol Rep Original Articles The study of vascular regulation often omits important information about the elastic properties of arteries under conditions of pulsatile flow. The purpose of this study was to examine the relationship between muscle sympathetic nerve activity (MSNA), vascular bed compliance, and peripheral blood flow responses in humans. We hypothesized that increases in MSNA would correlate with reductions in vascular compliance, and that changes in compliance would correspond with changes in peripheral blood flow during sympatho‐excitation. MSNA (microneurography), blood pressure (Finopres), and brachial artery blood flow (Doppler ultrasound), were monitored in six healthy males at baseline and during the last 15 s of voluntary end‐inspiratory, expiratory apneas and 5 min of static handgrip exercise (SHG; 20% maximum voluntary contraction) and 3 min of post‐exercise circulatory occlusion (SHG + PECO; measured in the non‐exercising arm). A lumped Windkessel model was employed to examine vascular bed compliance. During apnea, indices of MSNA were inversely related with vascular compliance, and reductions in compliance correlated with decreased brachial blood flow rate. During SHG, despite increased MSNA, compliance also increased, but was unrelated to increases in blood flow. Neither during SHG nor PECO did indices of MSNA correlate with forearm vascular compliance nor did vascular compliance correlate with brachial flow. However, during PECO, a linear combination of blood pressure and total MSNA was correlated with vascular compliance. These data indicate the elastic components of the forearm vasculature are regulated by adrenergic and myogenic mechanisms during sympatho‐excitation, but in a reflex‐dependent manner. John Wiley and Sons Inc. 2022-04-19 /pmc/articles/PMC9017978/ /pubmed/35439367 http://dx.doi.org/10.14814/phy2.15256 Text en © 2022 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Articles
Olver, T. Dylan
Badrov, Mark B.
Allen, Matti D.
Coverdale, Nicole S.
Shoemaker, J. Kevin
Acute changes in forearm vascular compliance during transient sympatho‐excitation
title Acute changes in forearm vascular compliance during transient sympatho‐excitation
title_full Acute changes in forearm vascular compliance during transient sympatho‐excitation
title_fullStr Acute changes in forearm vascular compliance during transient sympatho‐excitation
title_full_unstemmed Acute changes in forearm vascular compliance during transient sympatho‐excitation
title_short Acute changes in forearm vascular compliance during transient sympatho‐excitation
title_sort acute changes in forearm vascular compliance during transient sympatho‐excitation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017978/
https://www.ncbi.nlm.nih.gov/pubmed/35439367
http://dx.doi.org/10.14814/phy2.15256
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