Acute effects of strength exercises and effects of regular strength training on cell free DNA concentrations in blood plasma

被引:16
|
作者
Tug, Suzan [1 ]
Tross, Anna-Katharina [1 ]
Hegen, Patrick [2 ]
Neuberger, Elmo Wanja Immanuel [1 ]
Helmig, Susanne [1 ]
Schoellhorn, Wolfgang [2 ]
Simon, Perikles [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Sports Med Dis Prevent & Rehabil, Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Training & Movement Sci, Mainz, Germany
来源
PLOS ONE | 2017年 / 12卷 / 09期
关键词
INFLAMMATION; MARKERS; TRAPS;
D O I
10.1371/journal.pone.0184668
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Creatine kinase (CK) is a marker for muscle cell damage with limited potential as marker for training load in strength training. Recent exercise studies identified cell free DNA (cfDNA) as a marker for aseptic inflammation and cell damage. Here we overserved in a pilot study the acute effects during strength exercise and chronic effects of regular strength training on cfDNA concentrations over a period of four weeks in three training groups applying conservation training (CT) at 60% of the 1 repetition maximum, high intensity-low repetition training (HT) at 90% of the 1 repetition maximum and differential training (DT) at 60% of the 1 repetition maximum. EDTA-plasma samples were collected before every training session, and on the first and last training day repeatedly after every set of exercises. CfDNA increased significantly by 1.62-fold (mean (+/- SD) before first exercise: 8.31 (2.84) ng/ml, after last exercise 13.48 (4.12) ng/ml) across all groups within a single training session (p < 0.001). The increase was 1.77-fold higher (mean (+/- SD) before first exercise: 12.23 (6.29) ng/ml, after last exercise 17.73 (11.24) ng/ml) in HT compared to CT (mean (+/- SD) before first exercise: 6.79 (1.28) ng/ml, after last exercise 10.05 (2.89) ng/ml) (p = 0.01). DNA size analysis suggested predominant release of short, mononucleosomal DNA-fragments in the acute exercise setting, while we detected an increase of mostly longer, polynucleosomal cfDNA-fragments at rest before the training session only at day two with a subsequent return to baseline (p < 0.001). In contrast, training procedures did not cause any alterations in CK. Our results suggest that during strength exercise short-fragmented cfDNA is released, reflecting a fast, aseptic inflammatory response, while elevation of longer fragments at baseline on day two seemed to reflect mild cellular damage due to a novel training regime. We critically discuss the implications of our findings for future evaluations of cfDNA as a marker for training load in strength training.
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页数:12
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