首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Ethylene glycol dimethacrylate and diethylene glycol dimethacrylate exhibits cytotoxic and genotoxic effect on human gingival fibroblasts via induction of reactive oxygen species
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Ethylene glycol dimethacrylate and diethylene glycol dimethacrylate exhibits cytotoxic and genotoxic effect on human gingival fibroblasts via induction of reactive oxygen species

机译:乙二醇二甲基丙烯酸酯和二甘醇二甲基丙烯酸酯通过诱导反应性氧物种对人体牙龈成纤维细胞进行细胞毒性和遗传毒性作用

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摘要

Although methacrylic acid derivatives in their polymeric form are considered to be safe, insufficient polymerization and the release of monomers due to either mechanical or enzymatical factors can lead to their reaching millimolar concentrations in local tissue. The present study evaluates the effect of two methacrylate monomers - ethylene glycol dimethacrylate (EGDMA) and diethylene glycol dimethacrylate (DEGDMA)- on human gingival fibroblasts (HGFs). Both monomers were found to reduce cells viability in MIT assay, increase apoptosis and cause cell cycle arrest in G1/G0 phase. They also increased intracellular reactive oxygen species (ROS) production as measured by DCFH-DA and DHE probes and increased expression of GPx4 and SOD2. Both monomers increased DNA damage in comet assay. Moreover, HGFs were not able to repair those lesions within 120 min of repair incubation. However, the monomers were not found to have any effect on the integrity of isolated plasmids. We postulate that EGDMA and DEGDMA exhibit their cytotoxic and genotoxic properties via increased production of ROS, which cause DNA damage, affect apoptosis, viability and cell cycle. Further studies are needed to better understand the properties of methacrylic acid monomers and to evaluate the risk that they cause for patients, dentists and dental technicians.
机译:尽管其聚合物形式的甲基丙烯酸衍生物被认为是安全的,聚合不足,并且由于机械或酶促因子引起的单体的释放可以导致它们在局部组织中达到毫米浓度。本研究评估了两种甲基丙烯酸酯单体 - 乙二醇二甲基丙烯酸酯(EGDMA)和二甘醇二甲基丙烯酸二丙烯酸二丙烯酸酯(DEGDMA) - 对人牙龈成纤维细胞(HGF)的影响。发现两种单体在麻省理工学院测定中降低细胞活力,增加凋亡,并导致G1 / G0相中的细胞周期停滞。它们还增加了通过DCFH-DA和DHE探针测量的细胞内反应性氧物质(ROS)产生和GPX4和SOD2的表达增加。两种单体在彗星测定中增加了DNA损伤。此外,HGF不能在修复孵化的120分钟内修复这些病变。然而,未发现单体对分离的质粒的完整性产生任何影响。我们假设EGDMA和DEGDMA通过增加ROS的产量表现出它们的细胞毒性和遗传毒性特性,这导致DNA损伤,影响凋亡,活力和细胞周期。需要进一步研究以更好地了解甲基丙烯酸单体的性质,并评估它们导致患者,牙医和牙科技师的风险。

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