Department of Internal Medicine, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Dig Dis Sci. 2023 May;68(5):1824-1834. doi: 10.1007/s10620-022-07781-5. Epub 2022 Dec 7.
Nonsteroidal anti-inflammatory drug (NSAID)-induced enteropathy, the mechanism of which is involved in oxidative stress, can be lethal due to hemorrhage. Thus, we aimed to investigate the effect of hydrogen-rich water (HRW), in terms of oxidative stress, on intestinal mucosal damage as well as changes in the gut microbiome and the short-chain fatty acids (SCFAs) content in feces.
Hydrogen-rich water was orally administered for 5 days to investigate the effectiveness of indomethacin-induced enteropathy in mice. Small intestinal damage and luminal reactive oxygen species (ROS) were evaluated to investigate the ameliorating effects of hydrogen. Then, components of the gut microbiome were analyzed; fecal microbiota transplantation (FMT) was performed using the cecal contents obtained from mice drinking HRW. The cecal contents were analyzed for the SCFAs content. Finally, cells from the macrophage cell line RAW264 were co-cultured with the supernatants of cecal contents.
Hydrogen-rich water significantly ameliorated IND-induced enteropathy histologically and reduced the expression of IND-induced inflammatory cytokines. Microscopic evaluation revealed that luminal ROS was significantly reduced and that HRW did not change the gut microbiota; however, FMT from HRW-treated animals ameliorated IND-induced enteropathy. The SCFA content in the cecal contents of HRW-treated animals was significantly higher than that in control animals. The supernatant had significantly increased interleukin-10 expression in RAW264 cells in vitro.
Hydrogen-rich water ameliorated NSAID-induced enteropathy, not only via direct antioxidant effects but also via anti-inflammatory effects by increasing luminal SCFAs. These results suggest that hydrogen may have therapeutic potential in small intestinal inflammatory diseases.
非甾体抗炎药(NSAID)诱导的肠病,其机制涉及氧化应激,可因出血而致命。因此,我们旨在研究富氢水(HRW)在氧化应激方面对肠道黏膜损伤以及肠道微生物组和粪便短链脂肪酸(SCFAs)含量变化的影响。
通过口服 HRW 5 天来研究吲哚美辛诱导的肠病在小鼠中的有效性。评估小肠损伤和管腔活性氧(ROS)以研究氢的改善作用。然后,分析肠道微生物组的成分;使用来自饮用 HRW 的小鼠的盲肠内容物进行粪便微生物群移植(FMT)。分析盲肠内容物的 SCFAs 含量。最后,将巨噬细胞 RAW264 细胞与盲肠内容物的上清液共培养。
HRW 显著改善了 IND 诱导的肠病的组织学表现,并降低了 IND 诱导的炎症细胞因子的表达。显微镜评估显示管腔 ROS 显著减少,HRW 不改变肠道微生物组;然而,来自 HRW 处理动物的 FMT 改善了 IND 诱导的肠病。HRW 处理动物的盲肠内容物中的 SCFA 含量明显高于对照组。上清液在体外显著增加了 RAW264 细胞中白细胞介素 10 的表达。
HRW 通过直接抗氧化作用以及通过增加管腔 SCFAs 来发挥抗炎作用,改善了 NSAID 诱导的肠病。这些结果表明,氢在小肠炎症性疾病中可能具有治疗潜力。