Oxidative stress biomarkers responses to physical overtraining: Implications for diagnosis

被引:227
作者
Margonis, Konstantinos
Fatouros, Ioannis G. [1 ]
Jamurtas, Athanasios Z.
Nikolaidis, Michalis G.
Douroudos, Loannis
Chatzinikolaou, Athanasios
Mitrakou, Asimina
Mastorakos, George
Papassotiriou, Loannis
Taxildaris, Kiriakos
Kouretas, Dimitrios
机构
[1] Democritus Univ Thrace, Dept Phys Educ & Sport Sci, Komotini 69100, Greece
[2] Ctr Res & Technol, Inst Human Performance & Rehabil, Thessaly 42100, Trikala, Greece
[3] Univ Thessaly, Dept Phys Educ & Sport Sci, Trikala 42100, Greece
[4] Univ Thessaly, Dept Biochem & Biotechnol, Larisa 41221, Greece
[5] Henry Dunant Hosp, Dept Internal Med, Athens 11527, Greece
[6] Univ Athens, Aretaieion Hosp, Endocrine Unit, Dept Obstet & Gynecol,Sch Med, Athens 11526, Greece
[7] Aghia Sophia Childrens Hosp, Dept Clin Biochem, Athens 11527, Greece
关键词
overtraining; resistance exercise; antioxidant stains; oxidative stress bioinarkers;
D O I
10.1016/j.freeradbiomed.2007.05.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 tonesAveek: T4, 2 tonesAveek), 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. lsoprostanes 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. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:901 / 910
页数:10
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