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Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes

The study aimed to investigate the impact of laboratory-controlled exertional and exertional-heat stress on concentrations of plasma endogenous endotoxin core antibody (EndoCAb). Forty-four (males n= 26 and females n= 18) endurance trained ( V̇ O (2max) 56.8min/kg/min) participants completed either:...

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Autores principales: Young, Pascale, Rauch, Christopher, Russo, Isabella, Gaskell, Stephanie, Davidson, Zoe, Costa, Ricardo J. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622302/
https://www.ncbi.nlm.nih.gov/pubmed/35426092
http://dx.doi.org/10.1055/a-1827-3124
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author Young, Pascale
Rauch, Christopher
Russo, Isabella
Gaskell, Stephanie
Davidson, Zoe
Costa, Ricardo J. S.
author_facet Young, Pascale
Rauch, Christopher
Russo, Isabella
Gaskell, Stephanie
Davidson, Zoe
Costa, Ricardo J. S.
author_sort Young, Pascale
collection PubMed
description The study aimed to investigate the impact of laboratory-controlled exertional and exertional-heat stress on concentrations of plasma endogenous endotoxin core antibody (EndoCAb). Forty-four (males n= 26 and females n= 18) endurance trained ( V̇ O (2max) 56.8min/kg/min) participants completed either: P1–2h high intensity interval running in 23°C ambient temperature (T (amb) ), P2–2h running at 60% V̇ O (2max) in 35°C T (amb) , or P3–3h running at 60% V̇ O (2max) in 23°C T (amb) . Blood samples were collected pre- and post-exercise to determine plasma IgM, IgA, and IgG concentrations. Overall resting pre-exercise levels for plasma Ig were 173MMU/ml, 37AMU/ml, and 79GMU/ml, respectively. Plasma IgM concentration did not substantially change pre- to post-exercise in all protocols, and the magnitude of pre- to post-exercise change for IgM was not different between protocols (p=0.135). Plasma IgA and IgG increased pre- to post-exercise in P2 only (p=0.017 and p=0.016, respectively), but remained within normative range (35–250MU/ml). P2 resulted in greater disturbances to plasma IgA (p=0.058) and IgG (p=0.037), compared with P1 and P3. No substantial differences in pre-exercise and exercise-associated change was observed for EndoCAb between biological sexes. Exertional and exertional-heat stress resulted in modest disturbances to systemic EndoCAb responses, suggesting EndoCAb biomarkers presents a low sensitivity response to controlled-laboratory experimental designs within exercise gastroenterology.
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spelling pubmed-96223022022-11-01 Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes Young, Pascale Rauch, Christopher Russo, Isabella Gaskell, Stephanie Davidson, Zoe Costa, Ricardo J. S. Int J Sports Med The study aimed to investigate the impact of laboratory-controlled exertional and exertional-heat stress on concentrations of plasma endogenous endotoxin core antibody (EndoCAb). Forty-four (males n= 26 and females n= 18) endurance trained ( V̇ O (2max) 56.8min/kg/min) participants completed either: P1–2h high intensity interval running in 23°C ambient temperature (T (amb) ), P2–2h running at 60% V̇ O (2max) in 35°C T (amb) , or P3–3h running at 60% V̇ O (2max) in 23°C T (amb) . Blood samples were collected pre- and post-exercise to determine plasma IgM, IgA, and IgG concentrations. Overall resting pre-exercise levels for plasma Ig were 173MMU/ml, 37AMU/ml, and 79GMU/ml, respectively. Plasma IgM concentration did not substantially change pre- to post-exercise in all protocols, and the magnitude of pre- to post-exercise change for IgM was not different between protocols (p=0.135). Plasma IgA and IgG increased pre- to post-exercise in P2 only (p=0.017 and p=0.016, respectively), but remained within normative range (35–250MU/ml). P2 resulted in greater disturbances to plasma IgA (p=0.058) and IgG (p=0.037), compared with P1 and P3. No substantial differences in pre-exercise and exercise-associated change was observed for EndoCAb between biological sexes. Exertional and exertional-heat stress resulted in modest disturbances to systemic EndoCAb responses, suggesting EndoCAb biomarkers presents a low sensitivity response to controlled-laboratory experimental designs within exercise gastroenterology. Georg Thieme Verlag KG 2022-07-22 /pmc/articles/PMC9622302/ /pubmed/35426092 http://dx.doi.org/10.1055/a-1827-3124 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Young, Pascale
Rauch, Christopher
Russo, Isabella
Gaskell, Stephanie
Davidson, Zoe
Costa, Ricardo J. S.
Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes
title Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes
title_full Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes
title_fullStr Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes
title_full_unstemmed Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes
title_short Plasma Endogenous Endotoxin Core Antibody Response to Exercise in Endurance Athletes
title_sort plasma endogenous endotoxin core antibody response to exercise in endurance athletes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622302/
https://www.ncbi.nlm.nih.gov/pubmed/35426092
http://dx.doi.org/10.1055/a-1827-3124
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