Effect of Melatonin Supplementation on Antioxidant Status and DNA Damage in High Intensity Trained Athletes.
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
melatonin supplementation (20 mg/d) | increase | plasma melatonin levels | melatonin-treated group | p<0.05 | increased | #1 |
melatonin supplementation (20 mg/d) | increase | total antioxidant capacity (TAC) | melatonin-treated group (MG) | p<0.05 | higher | #2 |
melatonin supplementation (20 mg/d) | increase | glutathione peroxidase (GPx) activity | melatonin-treated group (MG) | p<0.05 | higher | #3 |
melatonin supplementation (20 mg/d) | no change | superoxide dismutase (SOD) enzyme activity | melatonin-treated group (MG) | null | no differences were found | #4 |
melatonin supplementation (20 mg/d) | decrease | DNA damage | melatonin-treated group (MG) | p<0.05 | diminished | #5 |
melatonin supplementation (20 mg/d) | increase | antioxidant status | high intensity interval training (HIIT) athletes | null | improves | #6 |
melatonin supplementation (20 mg/d) | decrease | DNA damage induced by high intensity training | high intensity interval training (HIIT) athletes | null | may prove to have beneficial effects preventing | #7 |
The aim of the study was to evaluate the effect of melatonin supplementation on antioxidant capacity and DNA damage in high intensity interval training (HIIT) athletes. A 2-week randomised, double-blinded, placebo-controlled trial with two groups was conducted. Placebo (PG) and melatonin (MG) (20 mg/d) athletes were monitored over a two-week period of HIIT and strength training. The total antioxidant capacity (TAC) and the glutathione peroxidase (GPx) and superoxide dismutase (SOD) activities were analysed in blood samples. DNA damage was measured in isolated lymphocytes by comet assay prior to and immediately after exercise. The supplementation increased plasma melatonin levels in the melatonin-treated group (p<0.05) after two weeks of intervention. Analysis of antioxidant status indicated higher (p<0.05) TAC and GPx in MG than PG post-intervention. No differences were found in SOD enzyme activity. DNA damage was diminished in MG (p<0.05) compared to PG in post-training conditions. Antioxidant status was associated with DNA damage (r=-0.679; p=0.047) in the melatonin-treated athletes. The present study suggest that melatonin supplementation improves antioxidant status and may prove to have beneficial effects preventing DNA damage induced by high intensity training.