Coldebella Cármen Regina, Ribeiro Ana Paula Dias, Sacono Nancy Tomoko, Trindade Flávia Zardo, Hebling Josimeri, Costa Carlos Alberto de Souza
Department of Orthodontics and Pediatric Dentistry, Araraquara Dental School, São Paulo State University, Araraquara, SP, Brazil.
Braz Dent J. 2009;20(4):267-74. doi: 10.1590/s0103-64402009000400001.
The aim of this study was to evaluate the trans-enamel and trans-dentinal effects of a 35% hydrogen peroxide (H2O2) bleaching gel on odontoblast-like cells. Enamel/dentin discs obtained from bovine incisors were mounted in artificial pulp chambers (APCs). Three groups were formed: G1- 35% H2O2; G2- 35% H2O2 + halogen light application; G3- control. The treatments were repeated 5 times and the APCs were incubated for 12 h. Then, the extract was collected and applied for 24 h on the cells. Cell metabolism, total protein dosage and cell morphology were evaluated. Cell metabolism decreased by 62.09% and 61.83% in G1 and G2, respectively. The depression of cell metabolism was statistically significant when G1 and G2 were compared to G3. Total protein dosage decreased by 93.13% and 91.80% in G1 and G2, respectively. The cells in G1 and G2 exhibited significant morphological alterations after contact with the extracts. Regardless of halogen light application, the extracts caused significantly more intense cytopathic effects compared to the control group. After 5 consecutive applications of a 35% H2O2 bleaching agent, either catalyzed or not by halogen light, products of gel degradation were capable to diffuse through enamel and dentin causing toxic effects to the cells.
本研究的目的是评估35%过氧化氢(H₂O₂)漂白凝胶对成牙本质细胞样细胞的穿釉质和穿牙本质作用。从牛切牙获得的釉质/牙本质圆盘被安装在人工牙髓腔(APC)中。形成三组:G1 - 35% H₂O₂;G2 - 35% H₂O₂ + 卤素光照射;G3 - 对照组。处理重复5次,APC孵育12小时。然后,收集提取物并作用于细胞24小时。评估细胞代谢、总蛋白含量和细胞形态。G1组和G2组的细胞代谢分别下降了62.09%和61.83%。当G1组和G2组与G3组比较时,细胞代谢的降低具有统计学意义。G1组和G2组的总蛋白含量分别下降了93.13%和91.80%。G1组和G2组的细胞在与提取物接触后表现出明显的形态改变。无论是否应用卤素光,与对照组相比,提取物引起的细胞病变效应明显更强烈。连续5次应用35% H₂O₂漂白剂后,无论是否由卤素光催化,凝胶降解产物都能够扩散穿过釉质和牙本质,对细胞产生毒性作用。