# Redox Water Consumption Attenuates Exercise-Induced Inflammation and Oxidative Stress in Physically Active Adults: A Randomized Controlled Trial

**Authors:** Anna Stolecka-Warzecha, Tomasz Zając, Marcin Gandyk, Maciej Kostrzewa, Ewa Sadowska-Krępa

PMC · DOI: 10.3390/nu18040694 · 2026-02-21

## TL;DR

Drinking redox water may reduce inflammation and oxidative stress after intense exercise in active adults, according to a small study.

## Contribution

This study is one of the first to investigate the biochemical effects of redox water on exercise-induced inflammation and oxidative stress in humans.

## Key findings

- Redox water consumption significantly reduced interleukin-6 (IL-6) levels after exercise compared to standard water.
- Lipid peroxidation levels remained stable in redox water consumers, while increasing in controls.
- Hematological and coagulation parameters were unaffected by redox water consumption.

## Abstract

Background: Acute high-intensity exercise induces transient inflammatory and oxidative stress responses, mediated by redox-sensitive signaling pathways and reflected by elevations in interleukin-6 (IL-6) and lipid peroxidation products. Modulation of these responses through hydration-based redox interventions remains insufficiently characterized at the biochemical level. Objective: This randomized controlled trial investigated whether regular consumption of redox (alkaline) water influences exercise-induced inflammatory and oxidative stress markers in physically active adults. Methods: Forty physically active adults were randomized into an experimental group (EG; n = 20) and consumed redox water subjected to molecular-level modification, yielding alkaline hydrogen-enriched water (pH 9.2–9.4), or a control group (CG; n = 20) that consumed standard water. After eight weeks of intervention, participants performed a standardized maximal aerobic exercise test. Plasma IL-6 and malondialdehyde (MDA) concentrations were measured at baseline and immediately post-exercise. Statistical analyses included two-way repeated measures ANOVA and ANCOVA. Results: A pronounced group × time interaction was observed for IL-6 (F(1,38) = 36.89, p < 0.001). The EG exhibited a significant post-exercise reduction in IL-6, whereas the CG demonstrated a robust increase. A significant group × time interaction was also detected for MDA (F(1,38) = 4.98, p = 0.029), reflecting stable lipid peroxidation levels in the EG and increased levels in the CG; however, baseline-adjusted analyses indicated that post-exercise MDA differences were largely attributable to initial variability. Hematological and coagulation parameters remained within physiological ranges in both groups. Conclusions: Redox water intake was associated with lower immediate post-exercise IL-6 compared with controls after baseline adjustment; however, pronounced baseline imbalance limits causal interpretation and warrants confirmation in larger trials with balanced inflammatory profiles. These findings highlight a potential biochemical mechanism linking hydration redox properties with inflammatory regulation during physical stress.

## Linked entities

- **Proteins:** IL6 (interleukin 6)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CAT (catalase) [NCBI Gene 847], SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}
- **Diseases:** type 2 diabetes (MESH:D003924), muscle soreness (MESH:D063806), muscle damage (MESH:D009133), Inflammation (MESH:D007249), neurodegenerative conditions (MESH:D019636), injury to (MESH:D014947), metabolic disturbances (MESH:D024821), coagulation (MESH:D001778), cardiovascular disease (MESH:D002318)
- **Chemicals:** water (MESH:D014867), lipid (MESH:D008055), Hydroxide (MESH:C031356), resveratrol (MESH:D000077185), hydrogen (MESH:D006859), TBARS (MESH:D017392), ROS (MESH:D017382), hydroxyl radicals (MESH:D017665), Alkaline water (-), superoxide (MESH:D013481), PUFA (MESH:D005231), oxygen (MESH:D010100), lactate (MESH:D019344), MDA (MESH:D008315)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943592/full.md

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Source: https://tomesphere.com/paper/PMC12943592