Ribeiro Daniel A, Matsumoto Mariza A, Marques Mariângela E A, Salvadori Daisy M F
Department of Health Sciences, Federal University of São Paulo, Botucatu, Brazil.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 May;103(5):e106-9. doi: 10.1016/j.tripleo.2006.11.024. Epub 2007 Feb 22.
Taking into consideration that DNA damage and cellular death play important roles during carcinogenesis, the purpose of the present study was to evaluate in vitro genotoxic or cytotoxic effects of chloroform and eucalyptol by single cell gel (comet) assay and trypan blue exclusion test, respectively.
Chloroform and eucalyptol were exposed to Chinese hamster ovary cells in culture directly for 3 hours at 37 degrees C at final concentrations ranging from 1.25 to 10 microL/mL. The negative control group was treated with vehicle control (phosphate-buffered solution), and the positive control group was treated with methyl metasulfonate (MMS, at 1 microg/mL concentration). All data were analyzed by the Kruskal-Wallis nonparametric test followed by the Dunn test.
The results showed that both gutta-percha solvents were cytotoxic at concentrations of 2.5, 5, and 10 microL/mL (P < .05). On the other hand, both solvents did not induce DNA breakage at 1.25 microL/mL concentration.
These results suggest that both chloroform or eucalyptol are strong cytotoxicants, but they may not be a factor that increases the level of DNA lesions in mammalian cells.
鉴于DNA损伤和细胞死亡在致癌过程中发挥重要作用,本研究的目的是分别通过单细胞凝胶(彗星)试验和台盼蓝排斥试验评估氯仿和桉叶油醇的体外遗传毒性或细胞毒性作用。
将氯仿和桉叶油醇在37℃下直接与培养的中国仓鼠卵巢细胞接触3小时,最终浓度范围为1.25至10微升/毫升。阴性对照组用载体对照(磷酸盐缓冲溶液)处理,阳性对照组用甲基磺酸甲酯(MMS,浓度为1微克/毫升)处理。所有数据通过Kruskal-Wallis非参数检验,随后进行Dunn检验进行分析。
结果表明,两种牙胶溶剂在浓度为2.5、5和10微升/毫升时具有细胞毒性(P <.05)。另一方面,两种溶剂在1.25微升/毫升浓度下均未诱导DNA断裂。
这些结果表明,氯仿或桉叶油醇都是强细胞毒性剂,但它们可能不是增加哺乳动物细胞中DNA损伤水平的因素。