Nocca Giuseppina, Callà Cinzia, Martorana Giuseppe Ettore, Cicillini Loredana, Rengo Sandro, Lupi Alessandro, Cordaro Massimo, Luisa Gozzo Maria, Spagnuolo Gianrico
Istituto di Biochimica e Biochimica Clinica, Facoltà di Medicina e Chirurgia, Università Cattolica del Sacro Cuore, Largo Francesco Vito 1, 00168 Rome, Italy.
Laboratorio di Patologia Clinica, Ospedale M.G. Vannini, Via dell'Acqua Bullicante, 00177 Rome, Italy.
Biomed Res Int. 2014;2014:956579. doi: 10.1155/2014/956579. Epub 2014 Feb 12.
Several studies have already demonstrated that the incomplete polymerization of resin-based dental materials causes the release of monomers which might affect cell metabolism. The aim of this study was to investigate the effects of triethylene glycol dimethacrylate, 1,4-butanediol dimethacrylate, urethane dimethacrylate, and 2-hydroxyethyl methacrylate on (1) cellular energy metabolism, evaluating oxygen consumption rate, glucose consumption, glucose 6-phosphate dehydrogenase activity, and lactate production, and (2) cellular redox status, through the evaluation of glutathione concentration and of the activities of enzymes regulating glutathione metabolism.
Human pulp cells were used and oxygen consumption was measured by means of a Clark electrode. Moreover, reactive oxygen species production was quantified. Enzymatic activity and glucose and lactate concentrations were determined through a specific kit.
Triethylene glycol dimethacrylate, 1,4-butanediol dimethacrylate, and 2-hydroxyethyl methacrylate induced a decrease in oxygen consumption rate, an enhancement of glucose consumption, and lactate production, whilst glucose 6-phosphate dehydrogenase and glutathione reductase activity were not significantly modified. Moreover, the monomers induced an increase of reactive oxygen species production with a consequent increase of superoxide dismutase and catalase enzymatic activities. A depletion of both reduced and total glutathione was also observed.
The obtained results indicate that dental monomers might alter energy metabolism and glutathione redox balance in human pulp cells.
多项研究已证明,树脂基牙科材料的不完全聚合会导致单体释放,这可能会影响细胞代谢。本研究的目的是调查三乙二醇二甲基丙烯酸酯、1,4 - 丁二醇二甲基丙烯酸酯、聚氨酯二甲基丙烯酸酯和甲基丙烯酸2 - 羟乙酯对(1)细胞能量代谢的影响,评估氧消耗率、葡萄糖消耗、葡萄糖6 - 磷酸脱氢酶活性和乳酸生成,以及(2)细胞氧化还原状态,通过评估谷胱甘肽浓度和调节谷胱甘肽代谢的酶的活性。
使用人牙髓细胞,通过克拉克电极测量氧消耗。此外,对活性氧的产生进行定量。通过特定试剂盒测定酶活性以及葡萄糖和乳酸浓度。
三乙二醇二甲基丙烯酸酯、1,4 - 丁二醇二甲基丙烯酸酯和甲基丙烯酸2 - 羟乙酯导致氧消耗率降低、葡萄糖消耗增加以及乳酸生成增加,而葡萄糖6 - 磷酸脱氢酶和谷胱甘肽还原酶活性未发生显著改变。此外,这些单体导致活性氧产生增加,随之超氧化物歧化酶和过氧化氢酶的酶活性增加。还观察到还原型谷胱甘肽和总谷胱甘肽均减少。
所得结果表明,牙科单体可能会改变人牙髓细胞中的能量代谢和谷胱甘肽氧化还原平衡。