Cargando…

Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences

Previous studies in animal models showed that exercise-induced metabolites accumulation may sensitize the mechanoreflex-induced response. The aim of this study was to assess whether the magnitude of the central hemodynamic and ventilatory adjustments evoked by isolated stimulation of the mechanorece...

Descripción completa

Detalles Bibliográficos
Autores principales: Laginestra, Fabio Giuseppe, Favaretto, Thomas, Giuriato, Gaia, Martignon, Camilla, Barbi, Chiara, Pedrinolla, Anna, Cavicchia, Alessandro, Venturelli, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363078/
https://www.ncbi.nlm.nih.gov/pubmed/37014452
http://dx.doi.org/10.1007/s00421-023-05186-4
_version_ 1785076563198345216
author Laginestra, Fabio Giuseppe
Favaretto, Thomas
Giuriato, Gaia
Martignon, Camilla
Barbi, Chiara
Pedrinolla, Anna
Cavicchia, Alessandro
Venturelli, Massimo
author_facet Laginestra, Fabio Giuseppe
Favaretto, Thomas
Giuriato, Gaia
Martignon, Camilla
Barbi, Chiara
Pedrinolla, Anna
Cavicchia, Alessandro
Venturelli, Massimo
author_sort Laginestra, Fabio Giuseppe
collection PubMed
description Previous studies in animal models showed that exercise-induced metabolites accumulation may sensitize the mechanoreflex-induced response. The aim of this study was to assess whether the magnitude of the central hemodynamic and ventilatory adjustments evoked by isolated stimulation of the mechanoreceptors in humans are influenced by the prior accumulation of metabolic byproducts in the muscle. 10 males and 10 females performed two exercise bouts consisting of 5-min of intermittent isometric knee-extensions performed 10% above the previously determined critical force. Post-exercise, the subjects recovered for 5 min either with a suprasystolic circulatory occlusion applied to the exercised quadriceps (PECO) or under freely-perfused conditions (CON). Afterwards, 1-min of continuous passive leg movement was performed. Central hemodynamics, pulmonary data, and electromyography from exercising/passively-moved leg were recorded throughout the trial. Root mean square of successive differences (RMSSD, index of vagal tone) was also calculated. Δpeak responses of heart rate (ΔHR) and ventilation ([Formula: see text] ) to passive leg movement were higher in PECO compared to CON (ΔHR: 6 ± 5 vs 2 ± 4 bpm, p = 0.01; 3.9 ± 3.4 vs 1.9 ± 1.7 L min(−1), p = 0.02). Δpeak of mean arterial pressure (ΔMAP) was significantly different between conditions (5 ± 3 vs  − 3 ± 3 mmHg, p < 0.01). Changes in RMSSD with passive leg movement were different between PECO and CON (p < 0.01), with a decrease only in the former (39 ± 18 to 32 ± 15 ms, p = 0.04). No difference was found in all the other measured variables between conditions (p > 0.05). These findings suggest that mechanoreflex-mediated increases in HR and [Formula: see text] are sensitized by metabolites accumulation. These responses were not influenced by biological sex.
format Online
Article
Text
id pubmed-10363078
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-103630782023-07-24 Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences Laginestra, Fabio Giuseppe Favaretto, Thomas Giuriato, Gaia Martignon, Camilla Barbi, Chiara Pedrinolla, Anna Cavicchia, Alessandro Venturelli, Massimo Eur J Appl Physiol Original Article Previous studies in animal models showed that exercise-induced metabolites accumulation may sensitize the mechanoreflex-induced response. The aim of this study was to assess whether the magnitude of the central hemodynamic and ventilatory adjustments evoked by isolated stimulation of the mechanoreceptors in humans are influenced by the prior accumulation of metabolic byproducts in the muscle. 10 males and 10 females performed two exercise bouts consisting of 5-min of intermittent isometric knee-extensions performed 10% above the previously determined critical force. Post-exercise, the subjects recovered for 5 min either with a suprasystolic circulatory occlusion applied to the exercised quadriceps (PECO) or under freely-perfused conditions (CON). Afterwards, 1-min of continuous passive leg movement was performed. Central hemodynamics, pulmonary data, and electromyography from exercising/passively-moved leg were recorded throughout the trial. Root mean square of successive differences (RMSSD, index of vagal tone) was also calculated. Δpeak responses of heart rate (ΔHR) and ventilation ([Formula: see text] ) to passive leg movement were higher in PECO compared to CON (ΔHR: 6 ± 5 vs 2 ± 4 bpm, p = 0.01; 3.9 ± 3.4 vs 1.9 ± 1.7 L min(−1), p = 0.02). Δpeak of mean arterial pressure (ΔMAP) was significantly different between conditions (5 ± 3 vs  − 3 ± 3 mmHg, p < 0.01). Changes in RMSSD with passive leg movement were different between PECO and CON (p < 0.01), with a decrease only in the former (39 ± 18 to 32 ± 15 ms, p = 0.04). No difference was found in all the other measured variables between conditions (p > 0.05). These findings suggest that mechanoreflex-mediated increases in HR and [Formula: see text] are sensitized by metabolites accumulation. These responses were not influenced by biological sex. Springer Berlin Heidelberg 2023-04-04 2023 /pmc/articles/PMC10363078/ /pubmed/37014452 http://dx.doi.org/10.1007/s00421-023-05186-4 Text en © The Author(s) 2023, corrected publication 2023 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 Original Article
Laginestra, Fabio Giuseppe
Favaretto, Thomas
Giuriato, Gaia
Martignon, Camilla
Barbi, Chiara
Pedrinolla, Anna
Cavicchia, Alessandro
Venturelli, Massimo
Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences
title Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences
title_full Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences
title_fullStr Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences
title_full_unstemmed Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences
title_short Concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences
title_sort concurrent metaboreflex activation increases chronotropic and ventilatory responses to passive leg movement without sex-related differences
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363078/
https://www.ncbi.nlm.nih.gov/pubmed/37014452
http://dx.doi.org/10.1007/s00421-023-05186-4
work_keys_str_mv AT laginestrafabiogiuseppe concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences
AT favarettothomas concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences
AT giuriatogaia concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences
AT martignoncamilla concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences
AT barbichiara concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences
AT pedrinollaanna concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences
AT cavicchiaalessandro concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences
AT venturellimassimo concurrentmetaboreflexactivationincreaseschronotropicandventilatoryresponsestopassivelegmovementwithoutsexrelateddifferences