Hydrogen Indirectly Suppresses Increases in Hydrogen Peroxide in Cytoplasmic Hydroxyl Radical-Induced Cells and Suppresses Cellular Senescence

Bacteria inhabiting the human gut metabolize microbiota-accessible carbohydrates (MAC) contained in plant fibers and subsequently release metabolic products. Gut bacteria produce hydrogen (H(2)), which scavenges the hydroxyl radical (•OH). Because H(2) diffuses within the cell, it is hypothesized th...

Descripción completa

Detalles Bibliográficos
Autores principales: Sakai, Takahiro, Kurokawa, Ryosuke, Hirano, Shin-ichi, Imai, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359316/
https://www.ncbi.nlm.nih.gov/pubmed/30669692
http://dx.doi.org/10.3390/ijms20020456
Descripción
Sumario:Bacteria inhabiting the human gut metabolize microbiota-accessible carbohydrates (MAC) contained in plant fibers and subsequently release metabolic products. Gut bacteria produce hydrogen (H(2)), which scavenges the hydroxyl radical (•OH). Because H(2) diffuses within the cell, it is hypothesized that H(2) 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 H(2) 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 H(2) into the cell culture medium. Cyto •OH-generated lipid peroxide caused glutathione (GSH) and heme shortage, increased hydrogen peroxide (H(2)O(2)), and induced cellular senescence via the phosphorylation of ataxia telangiectasia mutated kinase serine 1981 (p-ATM(ser1981))/p53 serine 15 (p-p53(ser15))/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, H(2) suppressed increased H(2)O(2) by suppressing cyto •OH-mediated lipid peroxide formation and cellular senescence induction via two pathways. H(2) produced by gut bacteria diffuses throughout the body to scavenge cyto •OH in cells. Therefore, it is highly likely that gut bacteria-produced H(2) is involved in intracellular maintenance of the redox state, thereby suppressing cellular senescence and individual aging. Hence, H(2) produced by intestinal bacteria may be involved in the suppression of aging.