Melatonin intake before intradialytic exercise reverses oxidative stress and improves antioxidant status in hemodialysis patients

Author:

Marzougui Houssem12ORCID,Turki Mouna13,Ben Dhia Imen24,Maaloul Rami12,Chaker Hanen56,Makhlouf Rihab13,Agrebi Ikram56,Kammoun Khawla56,Jamoussi Kamel7,Ayadi Fatma13,Ben Hmida Mohamed56,Hammouda Omar18

Affiliation:

1. Research Laboratory, Molecular Bases of Human Pathology, LR19ES13, Faculty of Medicine, University of Sfax, Sfax, Tunisia

2. High Institute of Sport and Physical Education of Sfax, University of Sfax, Sfax, Tunisia

3. Biochemistry Department, CHU Habib Bourguiba, University of Sfax, Sfax, Tunisia

4. Research Laboratory: Evaluation and Management of Musculoskeletal System Pathologies, LR20ES09, Faculty of Medicine, University of Sfax, Sfax, Tunisia

5. Nephrology Department, CHU Hedi Chaker, University of Sfax, Sfax, Tunisia

6. Research Laboratory of Renal Pathology, LR19ES11, Faculty of Medicine, University of Sfax, Sfax,Tunisia

7. Biochemistry Department, CHU Hedi Chaker, University of Sfax, Sfax, Tunisia

8. Interdisciplinary Laboratory in Neurosciences, Physiology and Psychology: Physical Activity, Health and Learning (LINP2), UFR STAPS, UPL, Paris Nanterre University, Nanterre, France

Abstract

Purpose: The present study aimed to investigate for the first time the effects of melatonin (MEL) intake on oxidative stress and cellular damage during intradialytic exercise (IEX). Methods: Thirteen hemodialysis (HD) patients volunteered to participate in the current randomized crossover trial. Participants performed four HD sessions in four different conditions: (Exercise (EX)-MEL), (EX-Placebo (PLA)), (Control (C)-MEL), and (C-PLA). 3 mg of MEL or PLA were taken 60 min before starting exercise, or at the equivalent time in the C conditions. Blood samples were taken before HD (T0), immediately after the end of IEX (T1), 60 min after IEX (T2), or at the corresponding times in the C conditions to measure free radicals damage, antioxidant biomarkers, as well as biomarkers of muscle and liver damage. Results: Malondialdehyde and Advanced Oxidation Protein Products decreased in (C-MEL) ( p < 0.05, d = 2.19; p < 0.01, d = 0.99, respectively) at T2 compared to T0. Catalase and total thiol levels increased in (C-MEL) ( p < 0.01, d = 1.51; p < 0.01, d = 1.56, respectively) and in (EX-MEL) ( p = 0.01, d = 1.28; p < 0.01, d = 1.52, respectively) at T1 compared to T0. Total bilirubin levels increased in (EX-MEL) and (C-MEL) at T2 compared to T0 ( p < 0.001, d = 2.77; p < 0.001, d = 1.36, respectively), but only at T2 compared to T1 in (EX-MEL) ( p < 0.001, d = 1.67). In all conditions, uric acid levels decreased at T1 compared to T0 and at T2 compared to T1, while biomarkers of muscle and liver damage remained unchanged. Conclusion: This pilot study is the first to show that MEL ingestion, alone or combined with IEX, could improve oxidant-antioxidant balance during HD.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,General Medicine,Medicine (miscellaneous),Bioengineering

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