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Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses
BACKGROUND: The study aims to compare how work-to-rest ratio (W:R) influences insulin sensitivity (S(i)) and inflammatory responses following one session of sprint interval training (SIT). METHODS: Thirteen men and two women completed a cross-over comparison of two SIT interventions—Tabata (TAB), 10...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773496/ https://www.ncbi.nlm.nih.gov/pubmed/27034919 http://dx.doi.org/10.1186/s40798-016-0044-1 |
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author | Harnish, Christopher R. Sabo, Roy T. |
author_facet | Harnish, Christopher R. Sabo, Roy T. |
author_sort | Harnish, Christopher R. |
collection | PubMed |
description | BACKGROUND: The study aims to compare how work-to-rest ratio (W:R) influences insulin sensitivity (S(i)) and inflammatory responses following one session of sprint interval training (SIT). METHODS: Thirteen men and two women completed a cross-over comparison of two SIT interventions—Tabata (TAB), 10 × 20-s sprints/10-s rest, and Wingate (WIN), 5 × 30-s sprints with 270-s rest. IL-6, IL-10, and TNF-α were assessed at baseline, immediately following, and 1 h after SIT, as well as prior to the 24-h post-exercise oral glucose tolerance tests (OGTTs). RESULTS: Participants were 23.8 (±3.5) years old and 180.0 (±10.2) cm tall, weighed 78.5 (13.0) kg, and had 16.9 (±6.5) % body fat, with a mean VO(2Peak) of 42.0 (±7.9) ml kg(−1) min(−1). There were no differences in total work (kJ) between TAB (64.7 ± 12.0) and WIN (68.0 ± 15.0). Mean (±95 % CI) S(i) 24 h changed −2.8 (−5.1, −0.5) from baseline after TAB and −3.9 (−6.9, −0.9) after WIN. Cytokines were measured in pg ml(−1) and expressed as mean change (±95 % CI). IL-6 increased significantly immediately following SIT for TAB 0.70 (0.23, 1.17), and WIN 1.11 (0.60, 1.62), and remained elevated 1 h post SIT for TAB 1.10 (0.37, 1.83), and WIN 0.95 (0.26, 1.65). IL-10 showed a significant positive change immediately following exercise for TAB 1.53 (0.77, 2.29) and WIN 1.59 (0.58, 2.59). TNF-α also increased immediately both TAB 3.26 (1.57, 4.96) and WIN 3.05 (0.56, 5.54) and was directly proportional to IL-10 (r = 0.64, p < 0.0001). CONCLUSIONS: W:R did not alter either the inflammatory or metabolic response following SIT nor does SIT improve 24-h S(i), despite increased levels of IL-10. |
format | Online Article Text |
id | pubmed-4773496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-47734962016-03-29 Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses Harnish, Christopher R. Sabo, Roy T. Sports Med Open Original Research Article BACKGROUND: The study aims to compare how work-to-rest ratio (W:R) influences insulin sensitivity (S(i)) and inflammatory responses following one session of sprint interval training (SIT). METHODS: Thirteen men and two women completed a cross-over comparison of two SIT interventions—Tabata (TAB), 10 × 20-s sprints/10-s rest, and Wingate (WIN), 5 × 30-s sprints with 270-s rest. IL-6, IL-10, and TNF-α were assessed at baseline, immediately following, and 1 h after SIT, as well as prior to the 24-h post-exercise oral glucose tolerance tests (OGTTs). RESULTS: Participants were 23.8 (±3.5) years old and 180.0 (±10.2) cm tall, weighed 78.5 (13.0) kg, and had 16.9 (±6.5) % body fat, with a mean VO(2Peak) of 42.0 (±7.9) ml kg(−1) min(−1). There were no differences in total work (kJ) between TAB (64.7 ± 12.0) and WIN (68.0 ± 15.0). Mean (±95 % CI) S(i) 24 h changed −2.8 (−5.1, −0.5) from baseline after TAB and −3.9 (−6.9, −0.9) after WIN. Cytokines were measured in pg ml(−1) and expressed as mean change (±95 % CI). IL-6 increased significantly immediately following SIT for TAB 0.70 (0.23, 1.17), and WIN 1.11 (0.60, 1.62), and remained elevated 1 h post SIT for TAB 1.10 (0.37, 1.83), and WIN 0.95 (0.26, 1.65). IL-10 showed a significant positive change immediately following exercise for TAB 1.53 (0.77, 2.29) and WIN 1.59 (0.58, 2.59). TNF-α also increased immediately both TAB 3.26 (1.57, 4.96) and WIN 3.05 (0.56, 5.54) and was directly proportional to IL-10 (r = 0.64, p < 0.0001). CONCLUSIONS: W:R did not alter either the inflammatory or metabolic response following SIT nor does SIT improve 24-h S(i), despite increased levels of IL-10. Springer International Publishing 2016-03-01 /pmc/articles/PMC4773496/ /pubmed/27034919 http://dx.doi.org/10.1186/s40798-016-0044-1 Text en © Harnish and Sabo. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Article Harnish, Christopher R. Sabo, Roy T. Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses |
title | Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses |
title_full | Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses |
title_fullStr | Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses |
title_full_unstemmed | Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses |
title_short | Comparison of Two Different Sprint Interval Training Work-to-Rest Ratios on Acute Inflammatory Responses |
title_sort | comparison of two different sprint interval training work-to-rest ratios on acute inflammatory responses |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773496/ https://www.ncbi.nlm.nih.gov/pubmed/27034919 http://dx.doi.org/10.1186/s40798-016-0044-1 |
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