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Acute responses of circulating microRNAs to low-volume sprint interval cycling

Low-volume high-intensity interval training is an efficient and practical method of inducing physiological responses in various tissues to develop physical fitness and may also change the expression of circulating microRNAs (miRNAs). The purpose of the present study was to examine whether miRNAs for...

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Autores principales: Cui, Shu Fang, Li, Wei, Niu, Jie, Zhang, Chen Yu, Chen, Xi, Ma, Ji Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626635/
https://www.ncbi.nlm.nih.gov/pubmed/26578983
http://dx.doi.org/10.3389/fphys.2015.00311
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author Cui, Shu Fang
Li, Wei
Niu, Jie
Zhang, Chen Yu
Chen, Xi
Ma, Ji Zheng
author_facet Cui, Shu Fang
Li, Wei
Niu, Jie
Zhang, Chen Yu
Chen, Xi
Ma, Ji Zheng
author_sort Cui, Shu Fang
collection PubMed
description Low-volume high-intensity interval training is an efficient and practical method of inducing physiological responses in various tissues to develop physical fitness and may also change the expression of circulating microRNAs (miRNAs). The purpose of the present study was to examine whether miRNAs for muscle, heart, somatic tissue and metabolism were affected by 30-s intervals of intensive sprint cycling. We also examined the relationship of these miRNAs to conventional biochemical and performance indices. Eighteen healthy young males performed sprint interval cycling. Circulating miRNAs in plasma were detected using TaqMan-based quantitative PCR and normalized to Let-7d/g/i. In addition, we determined the levels of insulin-like growth factor-I, testosterone and cortisol, and anaerobic capacity. Compared to plasma levels before exercise muscle-specific miR-1 (0.12 ± 0.02 vs. 0.09 ± 0.02), miR-133a (0.46 ± 0.10 vs. 0.31 ± 0.06), and miR-133b (0.19 ± 0.02 vs. 0.10 ± 0.01) decreased (all P < 0.05), while miR-206 and miR-499 remained unchanged. The levels of metabolism related miR-122 (0.62 ± 0.07 vs. 0.34 ± 0.03) and somatic tissues related miR-16 (1.74 ± 0.27 vs. 0.94 ± 0.12) also decreased (both P < 0.05). The post-exercise IGF-1 and cortisol concentrations were significantly increased, while testosterone concentrations did not. Plasma levels of miR-133b correlated to peak power (r = 0.712, P = 0.001) and miR-122 correlated to peak power ratio (r = 0.665, P = 0.003). In conclusion sprint exercise provokes genetic changes for RNA related to specific muscle or metabolism related miRNAs suggesting that miR-133b and miR-122 may be potential useful biomarkers for actual physiological strain or anaerobic capacity. Together, our findings on the circulating miRNAs may provide new insight into the physiological responses that are being performed during exercise and delineate mechanisms by which exercise confers distinct phenotypes and improves performance.
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spelling pubmed-46266352015-11-17 Acute responses of circulating microRNAs to low-volume sprint interval cycling Cui, Shu Fang Li, Wei Niu, Jie Zhang, Chen Yu Chen, Xi Ma, Ji Zheng Front Physiol Physiology Low-volume high-intensity interval training is an efficient and practical method of inducing physiological responses in various tissues to develop physical fitness and may also change the expression of circulating microRNAs (miRNAs). The purpose of the present study was to examine whether miRNAs for muscle, heart, somatic tissue and metabolism were affected by 30-s intervals of intensive sprint cycling. We also examined the relationship of these miRNAs to conventional biochemical and performance indices. Eighteen healthy young males performed sprint interval cycling. Circulating miRNAs in plasma were detected using TaqMan-based quantitative PCR and normalized to Let-7d/g/i. In addition, we determined the levels of insulin-like growth factor-I, testosterone and cortisol, and anaerobic capacity. Compared to plasma levels before exercise muscle-specific miR-1 (0.12 ± 0.02 vs. 0.09 ± 0.02), miR-133a (0.46 ± 0.10 vs. 0.31 ± 0.06), and miR-133b (0.19 ± 0.02 vs. 0.10 ± 0.01) decreased (all P < 0.05), while miR-206 and miR-499 remained unchanged. The levels of metabolism related miR-122 (0.62 ± 0.07 vs. 0.34 ± 0.03) and somatic tissues related miR-16 (1.74 ± 0.27 vs. 0.94 ± 0.12) also decreased (both P < 0.05). The post-exercise IGF-1 and cortisol concentrations were significantly increased, while testosterone concentrations did not. Plasma levels of miR-133b correlated to peak power (r = 0.712, P = 0.001) and miR-122 correlated to peak power ratio (r = 0.665, P = 0.003). In conclusion sprint exercise provokes genetic changes for RNA related to specific muscle or metabolism related miRNAs suggesting that miR-133b and miR-122 may be potential useful biomarkers for actual physiological strain or anaerobic capacity. Together, our findings on the circulating miRNAs may provide new insight into the physiological responses that are being performed during exercise and delineate mechanisms by which exercise confers distinct phenotypes and improves performance. Frontiers Media S.A. 2015-10-30 /pmc/articles/PMC4626635/ /pubmed/26578983 http://dx.doi.org/10.3389/fphys.2015.00311 Text en Copyright © 2015 Cui, Li, Niu, Zhang, Chen and Ma. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Cui, Shu Fang
Li, Wei
Niu, Jie
Zhang, Chen Yu
Chen, Xi
Ma, Ji Zheng
Acute responses of circulating microRNAs to low-volume sprint interval cycling
title Acute responses of circulating microRNAs to low-volume sprint interval cycling
title_full Acute responses of circulating microRNAs to low-volume sprint interval cycling
title_fullStr Acute responses of circulating microRNAs to low-volume sprint interval cycling
title_full_unstemmed Acute responses of circulating microRNAs to low-volume sprint interval cycling
title_short Acute responses of circulating microRNAs to low-volume sprint interval cycling
title_sort acute responses of circulating micrornas to low-volume sprint interval cycling
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626635/
https://www.ncbi.nlm.nih.gov/pubmed/26578983
http://dx.doi.org/10.3389/fphys.2015.00311
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