水素水による運動誘発性疲労軽減のメカニズム:IRG1-イタコン酸/Nrf2/HO-1経路の活性化
Using a mouse model of exercise-induced fatigue, this study investigated the molecular mechanisms underlying the fatigue-reducing effects of hydrogen-rich water. Administration of hydrogen-rich water improved motor function and reduced fatigue-associated biomarkers including blood urea nitrogen, lactate, and creatine kinase, while also attenuating gastrocnemius muscle damage. Ultrahigh-performance liquid chromatography-mass spectrometry analysis revealed that hydrogen-rich water elevated immunoresponsive gene 1 (IRG1) expression, restored fatigue-suppressed itaconic acid levels, and subsequently activated the downstream Nrf2/heme oxygenase-1 (HO-1) signaling pathway. Complementary experiments in C2C12 cells using an IRG1 inhibitor or 4-octyl itaconic acid confirmed that hydrogen-rich water upregulated Nrf2 and HO-1 expression at the cellular level. Collectively, these findings indicate that the IRG1-itaconate/Nrf2/HO-1 axis mediates oxidative stress suppression as a key mechanism by which hydrogen-rich water reduces exercise-induced fatigue.
Hydrogen-rich water upregulates IRG1 expression, restoring itaconic acid levels suppressed by exercise, which in turn activates the Nrf2/HO-1 antioxidant pathway and reduces oxidative stress-driven fatigue.
Hydrogen-rich water is a low-risk delivery route, but the achievable systemic hydrogen dose is bounded. For clinical applications, inhalation is the most efficient route; inhalation, however, carries explosion risk, and concentration matters (empirical LFL of 10% applies to inhalation environments; high-concentration devices are documented in the Consumer Affairs Agency accident database and are not recommended).
See also:
https://h2-papers.org/en/papers/40580185