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A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise
After a short historical account, and a discussion of Hill and Meyerhof’s theory of the energetics of muscular exercise, we analyse steady-state rest and exercise as the condition wherein coupling of respiration to metabolism is most perfect. The quantitative relationships show that the homeostatic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132876/ https://www.ncbi.nlm.nih.gov/pubmed/35217911 http://dx.doi.org/10.1007/s00421-022-04901-x |
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author | Ferretti, Guido Fagoni, Nazzareno Taboni, Anna Vinetti, Giovanni di Prampero, Pietro Enrico |
author_facet | Ferretti, Guido Fagoni, Nazzareno Taboni, Anna Vinetti, Giovanni di Prampero, Pietro Enrico |
author_sort | Ferretti, Guido |
collection | PubMed |
description | After a short historical account, and a discussion of Hill and Meyerhof’s theory of the energetics of muscular exercise, we analyse steady-state rest and exercise as the condition wherein coupling of respiration to metabolism is most perfect. The quantitative relationships show that the homeostatic equilibrium, centred around arterial pH of 7.4 and arterial carbon dioxide partial pressure of 40 mmHg, is attained when the ratio of alveolar ventilation to carbon dioxide flow ([Formula: see text] ) is − 21.6. Several combinations, exploited during exercise, of pertinent respiratory variables are compatible with this equilibrium, allowing adjustment of oxygen flow to oxygen demand without its alteration. During exercise transients, the balance is broken, but the coupling of respiration to metabolism is preserved when, as during moderate exercise, the respiratory system responds faster than the metabolic pathways. At higher exercise intensities, early blood lactate accumulation suggests that the coupling of respiration to metabolism is transiently broken, to be re-established when, at steady state, blood lactate stabilizes at higher levels than resting. In the severe exercise domain, coupling cannot be re-established, so that anaerobic lactic metabolism also contributes to sustain energy demand, lactate concentration goes up and arterial pH falls continuously. The [Formula: see text] decreases below − 21.6, because of ensuing hyperventilation, while lactate keeps being accumulated, so that exercise is rapidly interrupted. The most extreme rupture of the homeostatic equilibrium occurs during breath-holding, because oxygen flow from ambient air to mitochondria is interrupted. No coupling at all is possible between respiration and metabolism in this case. |
format | Online Article Text |
id | pubmed-9132876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-91328762022-05-27 A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise Ferretti, Guido Fagoni, Nazzareno Taboni, Anna Vinetti, Giovanni di Prampero, Pietro Enrico Eur J Appl Physiol Invited Review After a short historical account, and a discussion of Hill and Meyerhof’s theory of the energetics of muscular exercise, we analyse steady-state rest and exercise as the condition wherein coupling of respiration to metabolism is most perfect. The quantitative relationships show that the homeostatic equilibrium, centred around arterial pH of 7.4 and arterial carbon dioxide partial pressure of 40 mmHg, is attained when the ratio of alveolar ventilation to carbon dioxide flow ([Formula: see text] ) is − 21.6. Several combinations, exploited during exercise, of pertinent respiratory variables are compatible with this equilibrium, allowing adjustment of oxygen flow to oxygen demand without its alteration. During exercise transients, the balance is broken, but the coupling of respiration to metabolism is preserved when, as during moderate exercise, the respiratory system responds faster than the metabolic pathways. At higher exercise intensities, early blood lactate accumulation suggests that the coupling of respiration to metabolism is transiently broken, to be re-established when, at steady state, blood lactate stabilizes at higher levels than resting. In the severe exercise domain, coupling cannot be re-established, so that anaerobic lactic metabolism also contributes to sustain energy demand, lactate concentration goes up and arterial pH falls continuously. The [Formula: see text] decreases below − 21.6, because of ensuing hyperventilation, while lactate keeps being accumulated, so that exercise is rapidly interrupted. The most extreme rupture of the homeostatic equilibrium occurs during breath-holding, because oxygen flow from ambient air to mitochondria is interrupted. No coupling at all is possible between respiration and metabolism in this case. Springer Berlin Heidelberg 2022-02-26 2022 /pmc/articles/PMC9132876/ /pubmed/35217911 http://dx.doi.org/10.1007/s00421-022-04901-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Invited Review Ferretti, Guido Fagoni, Nazzareno Taboni, Anna Vinetti, Giovanni di Prampero, Pietro Enrico A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise |
title | A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise |
title_full | A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise |
title_fullStr | A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise |
title_full_unstemmed | A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise |
title_short | A century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise |
title_sort | century of exercise physiology: key concepts on coupling respiratory oxygen flow to muscle energy demand during exercise |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132876/ https://www.ncbi.nlm.nih.gov/pubmed/35217911 http://dx.doi.org/10.1007/s00421-022-04901-x |
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