首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Hydrogen Indirectly Suppresses Increases in Hydrogen Peroxide in Cytoplasmic Hydroxyl Radical-Induced Cells and Suppresses Cellular Senescence
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Hydrogen Indirectly Suppresses Increases in Hydrogen Peroxide in Cytoplasmic Hydroxyl Radical-Induced Cells and Suppresses Cellular Senescence

机译:氢间接抑制细胞质羟自由基诱导细胞中过氧化氢的增加并抑制细胞衰老

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摘要

Bacteria inhabiting the human gut metabolize microbiota-accessible carbohydrates (MAC) contained in plant fibers and subsequently release metabolic products. Gut bacteria produce hydrogen (H2), which scavenges the hydroxyl radical (•OH). Because H2 diffuses within the cell, it is hypothesized that H2 scavenges cytoplasmic •OH (cyto •OH) and suppresses cellular senescence. However, the mechanisms of cyto •OH-induced cellular senescence and the physiological role of gut bacteria-secreted H2 have not been elucidated. Based on the pyocyanin-stimulated cyto •OH-induced cellular senescence model, the mechanism by which cyto •OH causes cellular senescence was investigated by adding a supersaturated concentration of H2 into the cell culture medium. Cyto •OH-generated lipid peroxide caused glutathione (GSH) and heme shortage, increased hydrogen peroxide (H2O2), and induced cellular senescence via the phosphorylation of ataxia telangiectasia mutated kinase serine 1981 (p-ATMser1981)/p53 serine 15 (p-p53ser15)/p21 and phosphorylation of heme-regulated inhibitor (p-HRI)/phospho-eukaryotic translation initiation factor 2 subunit alpha serine 51 (p-eIF2α)/activating transcription factor 4 (ATF4)/p16 pathways. Further, H2 suppressed increased H2O2 by suppressing cyto •OH-mediated lipid peroxide formation and cellular senescence induction via two pathways. H2 produced by gut bacteria diffuses throughout the body to scavenge cyto •OH in cells. Therefore, it is highly likely that gut bacteria-produced H2 is involved in intracellular maintenance of the redox state, thereby suppressing cellular senescence and individual aging. Hence, H2 produced by intestinal bacteria may be involved in the suppression of aging.
机译:居住在人体肠道中的细菌代谢植物纤维中所含的微生物可及的碳水化合物(MAC),随后释放出代谢产物。肠道细菌会产生氢(H2),它会清除羟基(•OH)。由于H2在细胞内扩散,因此可以推测H2清除了细胞质•OH(细胞•OH)并抑制了细胞衰老。但是,尚未阐明细胞•OH诱导的细胞衰老的机制以及肠道细菌分泌的H2的生理作用。根据花青素刺激的细胞•OH诱导的细胞衰老模型,通过向细胞培养基中添加过饱和浓度的H2,研究了细胞•OH引起细胞衰老的机制。细胞•OH产生的脂质过氧化物导致谷胱甘肽(GSH)和血红素短缺,过氧化氢(H2O2)增加,并通过共济失调毛细血管扩张突变型激酶丝氨酸1981(p-ATM ser1981 )的磷酸化诱导细胞衰老。 / p53丝氨酸15(p-p53 ser15 )/ p21和血红素调节抑制剂(p-HRI)/磷酸化真核翻译起始因子2亚基α丝氨酸51(p-eIF2α)的磷酸化/激活转录因子4(ATF4)/ p16途径。此外,H2通过抑制细胞•OH介导的脂质过氧化物的形成和通过两种途径诱导细胞衰老来抑制H2O2的增加。肠道细菌产生的H2扩散到全身,清除细胞中的细胞•OH。因此,很有可能肠道细菌产生的H2参与了氧化还原状态的细胞内维持,从而抑制了细胞衰老和个体衰老。因此,肠细菌产生的H2可能参与了衰老的抑制。

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