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富氢水减轻运动性疲劳的机制:免疫反应基因1-衣康酸/核因子红细胞2相关因子2/血红素加氧酶-1途径的激活

Mechanism by which hydrogen-rich water mitigates exercise-induced fatigue: activation of the immunoresponsive gene 1-itaconate/nuclear factor erythroid 2-related factor 2/heme oxygenase-1 pathway.

作者信息

Zhang Yinyin, Ying Yajing, Zu Xianpeng, Ding Lingling, Shi Xuan, Wang Jing, Li Xiangtong, Li Chujian, Zhou Qicheng, Shen Hui, Li Hongxia, Lu Hongtao, Cheng Jin

机构信息

Department of Naval Medicine, Naval Medical University, Shanghai, China.

School of Pharmacy, Naval Medical University, Shanghai, China.

出版信息

Med Gas Res. 2026 Mar 1;16(1):26-32. doi: 10.4103/mgr.MEDGASRES-D-24-00148. Epub 2025 Jun 28.

DOI:10.4103/mgr.MEDGASRES-D-24-00148
PMID:40580185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12318582/
Abstract

JOURNAL/mgres/04.03/01612956-202603000-00005/figure1/v/2025-06-28T140100Z/r/image-tiff Exercise-induced fatigue limits athletic performance. Molecular hydrogen is an effective treatment for relieving fatigue, but the exact mechanism is not clear. In our study, a mouse model of fatigue was established to explore the molecular mechanism by which hydrogen-rich water reduces exercise-induced fatigue. The results showed that hydrogen-rich water improved the motor function of fatigue mice, reduced the levels of fatigue-related biomarkers (blood urea nitrogen, lactate, and creatine kinase), and alleviated gastrocnemius muscle injury. Furthermore, ultrahigh-performance liquid chromatography-mass spectrometry revealed that hydrogen-rich water upregulated the expression of immune response gene 1 (IRG1), increased the abnormally reduced levels of itaconic acid due to fatigue, and subsequently activated the downstream nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase 1 (HO-1) pathway. Finally, C2C12 cells exposed to an IRG1 inhibitor (IRG1-IN) or 4-octyl itaconic acid (4-OI) were treated with hydrogen-rich water, indicating that hydrogen-rich water effectively upregulated the expression of Nrf2 and HO-1 in cells. In summary, hydrogen-rich water alleviates exercise-induced fatigue by activating the IRG1-itaconic acid/Nrf2/HO-1 pathway and inhibiting oxidative stress.

摘要

《期刊》/mgres/04.03/01612956 - 202603000 - 00005/图1/v/2025 - 06 - 28T140100Z/图像 - 标签图像文件格式 运动诱导的疲劳会限制运动表现。分子氢是缓解疲劳的有效疗法,但其确切机制尚不清楚。在我们的研究中,建立了疲劳小鼠模型以探索富氢水减轻运动诱导疲劳的分子机制。结果表明,富氢水改善了疲劳小鼠的运动功能,降低了疲劳相关生物标志物(血尿素氮、乳酸和肌酸激酶)的水平,并减轻了腓肠肌损伤。此外,超高效液相色谱 - 质谱分析显示,富氢水上调了免疫反应基因1(IRG1)的表达,增加了因疲劳而异常降低的衣康酸水平,随后激活了下游核因子红细胞2相关因子2(Nrf2)/血红素加氧酶1(HO - 1)途径。最后,用富氢水处理暴露于IRG1抑制剂(IRG1 - IN)或4 - 辛基衣康酸(4 - OI)的C2C12细胞,表明富氢水有效上调了细胞中Nrf2和HO - 1的表达。总之,富氢水通过激活IRG1 - 衣康酸/Nrf2/HO - 1途径和抑制氧化应激来减轻运动诱导的疲劳。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/9f08aa009b95/MGR-16-26-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/248f3365e195/MGR-16-26-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/b9fa3f94f1ac/MGR-16-26-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/5d58a161865d/MGR-16-26-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/e3a6e58abd28/MGR-16-26-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/2715c359a318/MGR-16-26-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/9f08aa009b95/MGR-16-26-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/248f3365e195/MGR-16-26-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/b9fa3f94f1ac/MGR-16-26-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/5d58a161865d/MGR-16-26-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/e3a6e58abd28/MGR-16-26-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/2715c359a318/MGR-16-26-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/039c/12318582/9f08aa009b95/MGR-16-26-g007.jpg

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本文引用的文献

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Effects of 8 days intake of hydrogen-rich water on muscular endurance performance and fatigue recovery during resistance training.
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