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Original Article

Effect of antioxidant supplementation on leucocyte expression of reactive oxygen species in athletes

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Pages 526-533 | Received 23 May 2007, Accepted 11 Dec 2007, Published online: 08 Jul 2009
 

Abstract

Objective. Previous studies have shown that leucocytes, in particular granulocytes, have an enormous capacity for reactive oxygen species (ROS) production, and that this can be influenced by the physical activity of the individual. Theoretically, endurance‐trained athletes could profit by increasing their intake of antioxidants, thus neutralizing increased ROS production. The aim of the present investigation was to study the effect of dietary antioxidant supplementation on leucocyte ROS expression and total plasma antioxidant status (TAS) in endurance‐trained athletes over the course of 4 weeks. Methods. Eighteen athletes were recruited for the study. A randomized, double‐blinded, placebo‐controlled crossover study of 4 weeks of antioxidant supplementation (BiO‐Antioxidant 2.1 (400 mg vitamin C and 180 mg vitamin E d−1) and BiO‐Quinon Q10 (200 mg d−1)) was performed. Flow cytometry was applied to examine the leucocyte expression of ROS using the ROS‐sensitive probes dihydroethidium and dihydrorhodamine 123. The Randox Total Antioxidant Status kit was used to measure the plasma TAS of the athletes. Results. After 4 weeks of antioxidant supplementation, we observed no significant differences in ROS levels in granulocytes and monocytes either basally or after in vitro stimulation with phorbol myristate acetate. Plasma TAS did not change significantly during the intervention period. Conclusions. We observed no influence of 4 weeks of dietary antioxidant supplementation on oxidative stress status. Based on these findings, there is no rationale advising athletes to ingest antioxidant supplements in addition to their regular diet if that includes daily recommended doses of vitamins.

Acknowledgement

We thank Anne Lise Reiss, Lisbeth Saetre and Hanne Kleven for excellent technical and practical assistance.

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