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Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men

The aim of this study was to investigate the effect of a single dose of prednisolone on (A) high-intensity interval cycling performance and (B) post-exercise metabolic, hormonal and haematological responses. Nine young men participated in this double-blind, randomised, cross-over study. The particip...

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Autores principales: Tacey, Alexander, Parker, Lewan, Yeap, Bu B, Joseph, John, Lim, Ee M, Garnham, Andrew, Hare, David L, Brennan-Speranza, Tara, Levinger, Itamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373622/
https://www.ncbi.nlm.nih.gov/pubmed/30673629
http://dx.doi.org/10.1530/EC-18-0473
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author Tacey, Alexander
Parker, Lewan
Yeap, Bu B
Joseph, John
Lim, Ee M
Garnham, Andrew
Hare, David L
Brennan-Speranza, Tara
Levinger, Itamar
author_facet Tacey, Alexander
Parker, Lewan
Yeap, Bu B
Joseph, John
Lim, Ee M
Garnham, Andrew
Hare, David L
Brennan-Speranza, Tara
Levinger, Itamar
author_sort Tacey, Alexander
collection PubMed
description The aim of this study was to investigate the effect of a single dose of prednisolone on (A) high-intensity interval cycling performance and (B) post-exercise metabolic, hormonal and haematological responses. Nine young men participated in this double-blind, randomised, cross-over study. The participants completed exercise sessions (4 × 4 min cycling bouts at 90–95% of peak heart rate), 12 h after ingesting prednisolone (20 mg) or placebo. Work load was adjusted to maintain the same relative heart rate between the sessions. Exercise performance was measured as total work performed. Blood samples were taken at rest, immediately post exercise and up to 3 h post exercise. Prednisolone ingestion decreased total work performed by 5% (P < 0.05). Baseline blood glucose was elevated following prednisolone compared to placebo (P < 0.001). Three hours post exercise, blood glucose in the prednisolone trial was reduced to a level equivalent to the baseline concentration in the placebo trial (P > 0.05). Prednisolone suppressed the increase in blood lactate immediately post exercise (P < 0.05). Total white blood cell count was elevated at all time-points with prednisolone (P < 0.01). Androgens and sex hormone-binding globulin were elevated immediately after exercise, irrespective of prednisolone or placebo. In contrast, prednisolone significantly reduced the ratio of testosterone/luteinizing hormone (P < 0.01). Acute prednisolone treatment impairs high-intensity interval cycling performance and alters metabolic and haematological parameters in healthy young men. Exercise may be an effective tool to minimise the effect of prednisolone on blood glucose levels.
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spelling pubmed-63736222019-02-20 Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men Tacey, Alexander Parker, Lewan Yeap, Bu B Joseph, John Lim, Ee M Garnham, Andrew Hare, David L Brennan-Speranza, Tara Levinger, Itamar Endocr Connect Research The aim of this study was to investigate the effect of a single dose of prednisolone on (A) high-intensity interval cycling performance and (B) post-exercise metabolic, hormonal and haematological responses. Nine young men participated in this double-blind, randomised, cross-over study. The participants completed exercise sessions (4 × 4 min cycling bouts at 90–95% of peak heart rate), 12 h after ingesting prednisolone (20 mg) or placebo. Work load was adjusted to maintain the same relative heart rate between the sessions. Exercise performance was measured as total work performed. Blood samples were taken at rest, immediately post exercise and up to 3 h post exercise. Prednisolone ingestion decreased total work performed by 5% (P < 0.05). Baseline blood glucose was elevated following prednisolone compared to placebo (P < 0.001). Three hours post exercise, blood glucose in the prednisolone trial was reduced to a level equivalent to the baseline concentration in the placebo trial (P > 0.05). Prednisolone suppressed the increase in blood lactate immediately post exercise (P < 0.05). Total white blood cell count was elevated at all time-points with prednisolone (P < 0.01). Androgens and sex hormone-binding globulin were elevated immediately after exercise, irrespective of prednisolone or placebo. In contrast, prednisolone significantly reduced the ratio of testosterone/luteinizing hormone (P < 0.01). Acute prednisolone treatment impairs high-intensity interval cycling performance and alters metabolic and haematological parameters in healthy young men. Exercise may be an effective tool to minimise the effect of prednisolone on blood glucose levels. Bioscientifica Ltd 2019-01-23 /pmc/articles/PMC6373622/ /pubmed/30673629 http://dx.doi.org/10.1530/EC-18-0473 Text en © 2019 The authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Research
Tacey, Alexander
Parker, Lewan
Yeap, Bu B
Joseph, John
Lim, Ee M
Garnham, Andrew
Hare, David L
Brennan-Speranza, Tara
Levinger, Itamar
Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men
title Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men
title_full Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men
title_fullStr Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men
title_full_unstemmed Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men
title_short Single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men
title_sort single-dose prednisolone alters endocrine and haematologic responses and exercise performance in men
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373622/
https://www.ncbi.nlm.nih.gov/pubmed/30673629
http://dx.doi.org/10.1530/EC-18-0473
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