Soares Diana Gabriela, Ribeiro Ana Paula Dias, Lima Adriano Fonseca, Sacono Nancy Tomoko, Hebling Josimeri, de Souza Costa Carlos Alberto
Department of Dental Materials and Prosthodontics, Araraquara Dental School, UNESP - Univ Estadual Paulista, Araraquara, SP, Brazil.
Braz Dent J. 2013;24(2):121-7. doi: 10.1590/0103-6440201302161.
The aim of this study was to evaluate the possibility of fluoride solutions applied to enamel to protect pulp cells against the trans-enamel and transdentinal cytotoxicity of a 16% carbamide peroxide (CP) bleaching gel. The CP gel was applied to enamel/dentin discs adapted to aicial pulp chambers (8 h/day) during 1, 7 or 14 days, followed by fluoride (0.05% or 0.2%) application for 1 min. The extracts (culture medium in contact with dentin) were applied to MDPC-23 cells for 1 h, and cell metabolism (MTT assay), alkaline phosphatase (ALP) activity and cell membrane damage (flow cytometry) were analyzed. Knoop microhardness of enamel was also evaluated. Data were analyzed statistically by ANOVA and Kruskal-Wallis tests (α=0.05). For the MTT assay and ALP activity, significant reductions between the control and the bleached groups were observed (p<0.05). No statistically significant difference occurred among bleached groups (p>0.05), regardless of fluoride application or treatment days. Flow cytometry analysis demonstrated 30% of cell membrane damage in all bleached groups. After 14 days of treatment, the fluoride-treated enamel presented significantly higher microhardness values than the bleached-only group (p<0.05). It was concluded that, regardless of the increase in enamel hardness due to the application of fluoride solutions, the treated enamel surface did not prevent the toxic effects caused by the 16% CP gel to odontoblast-like cells.
本研究的目的是评估将氟溶液应用于牙釉质,以保护牙髓细胞免受16%过氧化脲(CP)漂白凝胶经牙釉质和牙本质的细胞毒性作用的可能性。将CP凝胶应用于适配人工牙髓腔的牙釉质/牙本质圆盘(每天8小时),持续1、7或14天,随后应用氟(0.05%或0.2%)1分钟。将提取物(与牙本质接触的培养基)应用于MDPC-23细胞1小时,并分析细胞代谢(MTT法)、碱性磷酸酶(ALP)活性和细胞膜损伤(流式细胞术)。还评估了牙釉质的努氏显微硬度。数据采用方差分析和克鲁斯卡尔-沃利斯检验进行统计学分析(α=0.05)。对于MTT法和ALP活性,观察到对照组和漂白组之间有显著降低(p<0.05)。无论是否应用氟或处理天数,漂白组之间均未出现统计学显著差异(p>0.05)。流式细胞术分析表明,所有漂白组均有30%的细胞膜损伤。处理14天后,经氟处理的牙釉质的显微硬度值显著高于仅漂白组(p<0.05)。得出的结论是,尽管应用氟溶液会使牙釉质硬度增加,但处理后的牙釉质表面并不能防止16% CP凝胶对成牙本质细胞样细胞产生的毒性作用。