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Independent and combined cytotoxicity and genotoxicity of triethylene glycol dimethacrylate and urethane dimethacrylate

机译:三乙二醇二甲基丙烯酸酯和尿烷二甲基丙烯酸酯的独立和联合细胞毒性和遗传毒性

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摘要

Dental composite materials contain polymers of methacrylates, which, due to mechanical abrasion and enzymatic action of saliva, may release their monomers into oral cavity and the pulp. Moreover, polymerization is always incomplete and leaves usually considerable fraction of free monomers. Mechanisms of the genotoxicity of methacrylate monomers have been rarely explored. As the polymerization of a monomer is catalyzed by a co-monomer, their combined action should be considered. In the present work, we investigated cytotoxic and genotoxic effects of urethane dimethacrylate (UDMA), often used as a monomer, at 1 mM, and triethylene glycol dimethacrylate (TEGDMA), a typical co-monomer, at 5 mM singly and in combination. Experiments were conducted on Chinese hamster ovary cells. Cell viability, apoptosis and cell cycle were assessed by flow cytometry, whereas DNA damage was evaluated by plasmid conformation test and comet assay. Both compounds decreased the viability of the cells, but did not induce strand breaks in an isolated plasmid DNA. However, both substances, either singly or in combination, damaged DNA in CHO cells as evaluated by comet assay. Both compounds induced apoptosis, but a combined action of them led to a decrease in the number of apoptotic cells. The combined action of UDMA and TEGDMA in the disturbance of cell cycle was lesser compared to the action of each compound individually. Individually, though UDMA and TEGDMA may induce cytotoxic and genotoxic, however, a combination of both does not produce a significant increase in these effects.
机译:牙科复合材料包含甲基丙烯酸酯聚合物,由于机械磨损和唾液的酶促作用,它们可能会将其单体释放到口腔和牙髓中。而且,聚合反应总是不完全的,通常会留下相当一部分游离单体。很少研究甲基丙烯酸酯单体的遗传毒性机理。由于单体的聚合是由共聚单体催化的,因此应考虑它们的联合作用。在目前的工作中,我们分别研究了氨基甲酸乙酯二甲基丙烯酸酯(UDMA)(通常用作单体)在1 mM时和典型的共聚单体三乙二醇二甲基丙烯酸酯(TEGDMA)在5 mM时的细胞毒性和遗传毒性作用。在中国仓鼠卵巢细胞上进行了实验。通过流式细胞术评估细胞活力,凋亡和细胞周期,而通过质粒构象测试和彗星试验评估DNA损伤。两种化合物均降低了细胞的活力,但未在分离的质粒DNA中诱导链断裂。然而,通过彗星分析评估,两种物质(单独或组合)均会破坏CHO细胞中的DNA。两种化合物均诱导凋亡,但它们的联合作用导致凋亡细胞数量减少。与每种化合物单独作用相比,UDMA和TEGDMA在细胞周期紊乱中的联合作用较小。单独地,尽管UDMA和TEGDMA可能会诱导细胞毒性和基因毒性,但是,两者的组合不会在这些作用中产生明显的增加。

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