ArticleJournal of dental sciences2025
Flammulina velutipes polysaccharides exhibit potent antioxidant and anti-pyroptotic properties in diabetes-associated periodontitis: A preliminary in vitro study.
Article in Journal of dental sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
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Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Biological activities and bioactive constituents of Flammulina velutipes: An updated systematic review.Journal of the science of food and agriculture · 2026Pooled it
- Effects of Various Drying Techniques on the Quality Attributes and Metabolite Profiles ofFoods (Basel, Switzerland) · 2026Article
- A scientometric study on research trends and characteristics of diabetes-associated periodontal disease.Journal of dental sciences · 2026Article
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Authors and funding
6 authors.
Funding
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Abstract
Background/purpose: Diabetes-associated periodontitis (DAP) is a complicated illness characterized by elevated oxidative stress and a pro-inflammatory response. There is a bidirectional relationship between diabetes and periodontitis. Although Materials and methods: Our study used HGFs treated with AGEs and LPS to mimic the in vitro environment of DAP. MTT assay was utilized to seek the various concentrations of FVP (a component of Results: Our study discovered that FVP exhibited minimal cytotoxicity to HGFs at the dosages examined. Co-treatment with AGEs and LPS dramatically reduced HGFs cell survival and migratory capacity, while considerably increasing intracellular ROS levels and expression of the cell senescence marker p16. However, the treatment of FVP restore these AGE and LPS-induced adverse effects, as evidenced by the restoration of cell survival and wound healing capacity, ROS production, and decrease the protein expression of p16. FVP inhibits AGEs and LPS-induced cell pyroptosis by lowering pyroptosis markers (apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC), NLR family pyrin domain containing 3 (NLRP3), caspase-1, gasdermin D (GSDMD), and IL-1β. Furthermore, FVP dramatically decreased proinflammatory cytokine production levels, including IL-6 and IL-8. Conclusion: The results of our study demonstrated that FVP had a significant protective effect on human gingival fibroblast damage caused by AGEs and LPS. The addition of FVP can reverse pathological processes such as cellular oxidative stress, poor wound healing, inflammaging, and pyroptosis caused by AGEs and LPS. These findings suggest that FVP could be effective as a therapeutic or adjuvant treatment for DAP.
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