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Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training

PURPOSE: The endurance training (ET)-induced increases in peak oxygen uptake ([Formula: see text] O(2peak)) and cardiac output ([Formula: see text] (peak)) during upright cycling are reversed to pre-ET levels after removing the training-induced increase in blood volume (BV). We hypothesised that ET-...

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Autores principales: Skattebo, Øyvind, Bjerring, Anders Wold, Auensen, Marius, Sarvari, Sebastian Imre, Cumming, Kristoffer Toldnes, Capelli, Carlo, Hallén, Jostein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181565/
https://www.ncbi.nlm.nih.gov/pubmed/32172291
http://dx.doi.org/10.1007/s00421-020-04336-2
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author Skattebo, Øyvind
Bjerring, Anders Wold
Auensen, Marius
Sarvari, Sebastian Imre
Cumming, Kristoffer Toldnes
Capelli, Carlo
Hallén, Jostein
author_facet Skattebo, Øyvind
Bjerring, Anders Wold
Auensen, Marius
Sarvari, Sebastian Imre
Cumming, Kristoffer Toldnes
Capelli, Carlo
Hallén, Jostein
author_sort Skattebo, Øyvind
collection PubMed
description PURPOSE: The endurance training (ET)-induced increases in peak oxygen uptake ([Formula: see text] O(2peak)) and cardiac output ([Formula: see text] (peak)) during upright cycling are reversed to pre-ET levels after removing the training-induced increase in blood volume (BV). We hypothesised that ET-induced improvements in [Formula: see text] O(2peak) and [Formula: see text] (peak) are preserved following phlebotomy of the BV gained with ET during supine but not during upright cycling. Arteriovenous O(2) difference (a-[Formula: see text] O(2)diff; [Formula: see text] O(2)/[Formula: see text] ), cardiac dimensions and muscle morphology were studied to assess their role for the [Formula: see text] O(2peak) improvement. METHODS: Twelve untrained subjects ([Formula: see text] O(2peak): 44 ± 6 ml kg(−1) min(−1)) completed 10 weeks of supervised ET (3 sessions/week). Echocardiography, muscle biopsies, haemoglobin mass (Hb(mass)) and BV were assessed pre- and post-ET. [Formula: see text] O(2peak) and [Formula: see text] (peak) during upright and supine cycling were measured pre-ET, post-ET and immediately after Hb(mass) was reversed to the individual pre-ET level by phlebotomy. RESULTS: ET increased the Hb(mass) (3.3 ± 2.9%; P = 0.005), BV (3.7 ± 5.6%; P = 0.044) and [Formula: see text] O(2peak) during upright and supine cycling (11 ± 6% and 10 ± 8%, respectively; P ≤ 0.003). After phlebotomy, improvements in [Formula: see text] O(2peak) compared with pre-ET were preserved in both postures (11 ± 4% and 11 ± 9%; P ≤ 0.005), as was [Formula: see text] (peak) (9 ± 14% and 9 ± 10%; P ≤ 0.081). The increased [Formula: see text] (peak) and a-[Formula: see text] O(2)diff accounted for 70% and 30% of the [Formula: see text] O(2peak) improvements, respectively. Markers of mitochondrial density (CS and COX-IV; P ≤ 0.007) and left ventricular mass (P = 0.027) increased. CONCLUSION: The ET-induced increase in [Formula: see text] O(2peak) was preserved despite removing the increases in Hb(mass) and BV by phlebotomy, independent of posture. [Formula: see text] O(2peak) increased primarily through elevated [Formula: see text] (peak) but also through a widened a-[Formula: see text] O(2)diff, potentially mediated by cardiac remodelling and mitochondrial biogenesis.
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spelling pubmed-71815652020-04-29 Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training Skattebo, Øyvind Bjerring, Anders Wold Auensen, Marius Sarvari, Sebastian Imre Cumming, Kristoffer Toldnes Capelli, Carlo Hallén, Jostein Eur J Appl Physiol Original Article PURPOSE: The endurance training (ET)-induced increases in peak oxygen uptake ([Formula: see text] O(2peak)) and cardiac output ([Formula: see text] (peak)) during upright cycling are reversed to pre-ET levels after removing the training-induced increase in blood volume (BV). We hypothesised that ET-induced improvements in [Formula: see text] O(2peak) and [Formula: see text] (peak) are preserved following phlebotomy of the BV gained with ET during supine but not during upright cycling. Arteriovenous O(2) difference (a-[Formula: see text] O(2)diff; [Formula: see text] O(2)/[Formula: see text] ), cardiac dimensions and muscle morphology were studied to assess their role for the [Formula: see text] O(2peak) improvement. METHODS: Twelve untrained subjects ([Formula: see text] O(2peak): 44 ± 6 ml kg(−1) min(−1)) completed 10 weeks of supervised ET (3 sessions/week). Echocardiography, muscle biopsies, haemoglobin mass (Hb(mass)) and BV were assessed pre- and post-ET. [Formula: see text] O(2peak) and [Formula: see text] (peak) during upright and supine cycling were measured pre-ET, post-ET and immediately after Hb(mass) was reversed to the individual pre-ET level by phlebotomy. RESULTS: ET increased the Hb(mass) (3.3 ± 2.9%; P = 0.005), BV (3.7 ± 5.6%; P = 0.044) and [Formula: see text] O(2peak) during upright and supine cycling (11 ± 6% and 10 ± 8%, respectively; P ≤ 0.003). After phlebotomy, improvements in [Formula: see text] O(2peak) compared with pre-ET were preserved in both postures (11 ± 4% and 11 ± 9%; P ≤ 0.005), as was [Formula: see text] (peak) (9 ± 14% and 9 ± 10%; P ≤ 0.081). The increased [Formula: see text] (peak) and a-[Formula: see text] O(2)diff accounted for 70% and 30% of the [Formula: see text] O(2peak) improvements, respectively. Markers of mitochondrial density (CS and COX-IV; P ≤ 0.007) and left ventricular mass (P = 0.027) increased. CONCLUSION: The ET-induced increase in [Formula: see text] O(2peak) was preserved despite removing the increases in Hb(mass) and BV by phlebotomy, independent of posture. [Formula: see text] O(2peak) increased primarily through elevated [Formula: see text] (peak) but also through a widened a-[Formula: see text] O(2)diff, potentially mediated by cardiac remodelling and mitochondrial biogenesis. Springer Berlin Heidelberg 2020-03-14 2020 /pmc/articles/PMC7181565/ /pubmed/32172291 http://dx.doi.org/10.1007/s00421-020-04336-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Skattebo, Øyvind
Bjerring, Anders Wold
Auensen, Marius
Sarvari, Sebastian Imre
Cumming, Kristoffer Toldnes
Capelli, Carlo
Hallén, Jostein
Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training
title Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training
title_full Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training
title_fullStr Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training
title_full_unstemmed Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training
title_short Blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training
title_sort blood volume expansion does not explain the increase in peak oxygen uptake induced by 10 weeks of endurance training
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181565/
https://www.ncbi.nlm.nih.gov/pubmed/32172291
http://dx.doi.org/10.1007/s00421-020-04336-2
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