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王翀, 段链, 顾雯, 阮鸿洁. 体外微核试验与基因突变试验比较[J]. 中国公共卫生, 2019, 35(11): 1510-1514. DOI: 10.11847/zgggws1120630
引用本文: 王翀, 段链, 顾雯, 阮鸿洁. 体外微核试验与基因突变试验比较[J]. 中国公共卫生, 2019, 35(11): 1510-1514. DOI: 10.11847/zgggws1120630
Chong WANG, Lian DUAN, Wen GU, . Application of in vitro mammalian cell micronucleus test and mammalian cell gene mutation test in genetic toxicity detection of hair dyes: a comparison study[J]. Chinese Journal of Public Health, 2019, 35(11): 1510-1514. DOI: 10.11847/zgggws1120630
Citation: Chong WANG, Lian DUAN, Wen GU, . Application of in vitro mammalian cell micronucleus test and mammalian cell gene mutation test in genetic toxicity detection of hair dyes: a comparison study[J]. Chinese Journal of Public Health, 2019, 35(11): 1510-1514. DOI: 10.11847/zgggws1120630

体外微核试验与基因突变试验比较

Application of in vitro mammalian cell micronucleus test and mammalian cell gene mutation test in genetic toxicity detection of hair dyes: a comparison study

  • 摘要:
      目的  通过2种方法检测3种市售染发剂,评价染发剂的遗传毒性并对最终结果进行比较。
      方法  选用小鼠淋巴瘤细胞(L5178Y)为细胞系进行体外微核(MNvit)试验和TK基因突变试验(MLA),MNvit试验经过细胞制片、染色、显微镜观察计数进行结果分析,TK MLA通过计算突变频率(MF)分析受试物是否具有遗传毒性。
      结果  MNvit试验结果显示,3种染发剂的实验组微核率与阴性对照组比较均有显著性差异(P < 0.05),确定MNvit试验为阳性。TK MLA结果显示3种染发剂与对照组比较差异具有显著性(P < 0.05)。样品3的MNvit试验结果虽最终判定为阳性,但在活化系统存在时却没有出现阳性结果。
      结论  通过对3种染发剂的检测,无论MNvit试验还是TK MLA,试验判定结果具有高度一致性。TK MLA耗时长,成本高,操作麻烦,可以考虑将MNvit试验作为遗传毒性另一种方法。但3种样品的体内微核试验结果却均为阴性,体外或体内微核试验用于检测染发剂的遗传毒性出现不同结果,有必要进一步探讨遗传毒性的测试组合。

     

    Abstract:
      Objective  To determine genetic toxicity of three market-available hair dyes with in vitro micronucleus test (MNvit) and thymidinekinase mouse lymphoma assay (TK MLA) and to compare detection results of the two methods.
      Methods  Mouse L5178Y cell line was used in the detections. In MNvit test, micronucleus rate was calculated by microscopic counting of the specimens after smearing and staining. In MLA, mutation frequency (MF) was calculated for the determination of genetic toxicity.
      Results  Significant differences in micronucleus rate were observed between experiment group and negative control group for all the 3 hair dyes in MNvit (P < 0.05 for all), indicating that all the 3 hair dyes are genetic toxicity positive. The MF of the experimental groups were significantly higher than that of the control group for all the 3 hair dyes in TK MLA (all P < 0.05). The sample of No. 3 hair dye was genetic toxicity positive in MNvit test only under the absence of S9 activation system.
      Conclusion  The genetic toxicity results of in vitro micronucleus test and TK gene mutation test are highly consistent for the 3 hair dyes detected. Due to TK gene mutation test being time and cost consuming and complicated in operation, micronucleus test in vitro can be considered as another genetic toxicity test. However, further studies are needed for combined genetic toxicity test because of the inconsistency between the genetic toxicity results of in vivo and in vitro micronucleus test.

     

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