Molecular hydrogen suppresses Porphyromonas gingivalis lipopolysaccharide‑induced increases in interleukin‑1 alpha and interleukin‑6 secretion in human gingival cells
Yasukazu Saitoh, Nene Yonekura, Daigo Matsuoka, Akira Matsumoto
Molecular and Cellular Biochemistry · 2022 · 477(1) · 99–104
Abstract
Periodontitis is defined as a multifactorial polymicrobial infection accompanied by inflammatory reactions. Porphyromonas gingivalis (Pg) is known as a major pathogen in the initiation and progression of periodontitis, and a major virulence factor is Pg lipopolysaccharide (LPS). Molecular hydrogen (H2) has been reported to act as a gaseous antioxidant, which suppresses periodontitis progression by decreasing gingival oxidative stress. However, no human periodontitis model has examined the anti-inflammatory effects of H2. In this study, we examined the effects of H2 on Pg LPS-induced secretion of 8 types of inflammation markers in a human periodontitis model using human gingival cells with enzyme-linked immunosorbent assays. Our results demonstrated that Pg LPS increased interleukin (IL) 1 alpha (IL-1α) and IL-6 secretion, but H2 significantly suppressed the secretion of both cytokines without cytotoxicity. H2 can suppress the production of IL-1α and IL-6, which are identified as cytokines involved in inflammatory reactions in periodontal disease. Thus, H2 may provide therapeutic applications for periodontitis.
Study details
- Article type
- Original Research
- Disease / injury model
- Periodontitis (Porphyromonas gingivalis LPS-induced inflammation in human gingival cells)
- Dose-dependent effect
- No
- Outcome
- Positive
- Findings
- Molecular hydrogen (H2) significantly suppressed Porphyromonas gingivalis LPS-induced increases in interleukin-1 alpha (IL-1α) and interleukin-6 (IL-6) secretion in human gingival epithelial cells, without cytotoxicity. H2 was more effective in suppressing IL-6 than IL-1α, suggesting potential therapeutic applications for periodontitis.
Classification
- Research Topics
- Study Type
- Species
- Organs & Tissues
- Physiological Systems
- Biomarkers
- Methods of Administration
- Countries
