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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Oxidative stress biomarkers responses to physical overtraining: Implications for diagnosis

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Author
Margonis, K.; Fatouros, I. G.; Jamurtas, A. Z.; Nikolaidis, M. G.; Douroudos, I.; Chatzinikolaou, A.; Mitrakou, A.; Mastorakos, G.; Papassotiriou, I.; Taxildaris, K.; Kouretas, D.
Date
2007
DOI
10.1016/j.freeradbiomed.2007.05.022
Keyword
Antioxidant status
Overtraining
Oxidative stress biomarkers
Resistance exercise
biological marker
carbonyl derivative
catalase
glutathione
glutathione disulfide
glutathione peroxidase
isoprostane
thiobarbituric acid reactive substance
adult
article
controlled study
correlational study
diagnostic procedure
human
human experiment
leukocytosis
male
muscle injury
overtraining syndrome
oxidative stress
priority journal
Antioxidants
Biological Markers
Humans
Leukocyte Count
Muscle Fatigue
Muscle, Skeletal
Physical Endurance
Metadata display
Abstract
Overtraining syndrome is characterized by declining performance and transient inflammation following periods of severe training with major health implications for the athletes. Currently, there is no single diagnostic marker for overtraining. The present investigation examined the responses of oxidative stress biomarkers to a resistance training protocol of progressively increased and decreased volume/intensity. Twelve males (21.3 ± 2.3 years) participated in a 12-week resistance training consisting of five 3-week periods (T1, 2 tones/week; T2, 8 tones/week; T3, 14 tones/week; T4, 2 tones/week), followed by a 3-week period of complete rest. Blood/urine samples were collected at baseline and 96 h following the last training session of each period. Performance (strength, power, jumping ability) increased after T2 and declined thereafter, indicating an overtraining response. Overtraining (T3) induced sustained leukocytosis, an increase of urinary isoprostanes (7-fold), TBARS (56%), protein carbonyls (73%), catalase (96%), glutathione peroxidase, and oxidized glutathione (GSSG) (25%) and a decline of reduced glutathione (GSH) (31%), GSH/GSSG (56%), and total antioxidant capacity. Isoprostanes and GSH/GSSG were highly (r = 0.764-0.911) correlated with performance drop and training volume increase. In conclusion, overtraining induces a marked response of oxidative stress biomarkers which, in some cases, was proportional to training load, suggesting that they may serve as a tool for overtraining diagnosis. © 2007 Elsevier Inc. All rights reserved.
URI
http://hdl.handle.net/11615/30722
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