H2S-Scavenging Hydrogel Alleviating Mitochondria Damage to Control Periodontitis

牙周炎 化学 牙周纤维 促炎细胞因子 炎症 氧化应激 透明质酸 生物膜 微生物学 细胞生物学 药理学 牙科 细菌 生物化学 免疫学 医学 生物 解剖 遗传学
作者
Chan Xie,Qing Zhang,Alberto Bianco,Shaohua Ge,Bo Ma
出处
期刊:Journal of Dental Research [SAGE]
标识
DOI:10.1177/00220345241291540
摘要

H 2 S, as a typical metabolite of periodontal pathogens, exhibits a clear positive correlation with the occurrence and development of periodontitis. H 2 S at physiological concentrations can regulate many biological processes. However, excess H 2 S in the periodontal pocket can trigger secretion of proinflammatory cytokines, cause oxidative stress, and result in mitochondrial damage and cell death in human gingival fibroblasts, exacerbating periodontitis development and periodontal tissue destruction. Worse, H 2 S facilitates bacteria survival and proliferation by maintaining bacterial redox balance and enhancing antibiotic resistance. Unfortunately, scavenging H 2 S during periodontitis treatment is usually ignored. Herein, a kind of hyaluronic acid methacryloyl/ZnO (HMZ) composite hydrogel with an H 2 S-scavenging ability was prepared to enhance periodontitis treatment. The HMZ hydrogel possessed good injectability and cytocompatibility and was able to remove H 2 S by a reaction with ZnO. As a result, the HMZ hydrogel was able to increase cell viability from 13% to 120% for human gingival fibroblasts and 22% to 94% for human periodontal ligament fibroblasts at 48 h, restore mitochondrial homeostasis, and alleviate cGAS-STING signaling pathway–mediated inflammation. Meanwhile, the HMZ hydrogel showed satisfactory antibacterial properties and efficiency of plaque biofilm removal. The in vivo results further confirmed that HMZ hydrogel decreased the concentration of H 2 S within the periodontal pocket from 0.7 to 0.8 mM to the normal level (0.3 to 0.4 mM), killed the bacteria in the periodontal tissues, inhibited osteoclast activity, relieved excess inflammation, and decreased the vertical distance between the cementoenamel junction and the alveolar bone crest from 1,175 µm to 798 µm on the 7th day and from 1,075 µm to 693 µm on the 14th day, achieving efficient periodontal bone regeneration. In brief, an H 2 S scavenging-based promising strategy was developed to enhance the therapeutic efficiency of periodontitis.
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