癌变·畸变·突变

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标准化Ames波动试验最佳条件的优选

陈  颖,李  莹,管  隽,王忠辉,贾玉玲,周  莉,孙祖越*   

  1. 上海市计划生育科学研究所药理毒理学研究室,中国生育调节药物毒理学检测中心,上海  200032
  • 收稿日期:2013-07-08 修回日期:2014-04-08
  • 通讯作者: 孙祖越,E-mail:sunzy64@163.com
  • 作者简介:陈 颖(1986- ),女,硕士,研究实习员,研究方向:药物遗传毒理学研究。E-mail:chyingbei @163.com
  • 基金资助:

    十二五“重大新药创制”科技重大专项(2011ZX09301-005),上海市实验动物创新行动计划项目(11140901300,11140901303), 上海市人才发展基金(2010031)

Optimization of standardized Ames fluctuation test

CHEN Ying,LI Ying,GUAN Jun,WANG Zhong-hui,JIA Yu-ling,ZHOU Li,SUN Zu-yue*   

  1. Department of Pharmacology and Toxicology, Shanghai Institute of Planned Parenthood Research, National Evaluation Center for the Toxicology of Fertility Regulation Drugs, Shanghai 200032, China
  • Received:2013-07-08 Revised:2014-04-08

摘要:

目的: 建立Ames波动试验的标准化方法,为其应用于化合物的遗传毒性检测奠定基础。方法:应用4种已知具有遗传毒性的阳性化合物敌克松(Dexon)、叠氮钠(SA)、环磷酰胺(CP)和2-氨基芴(2-AF)进行Ames波动试验。比较2种不同的增菌方法和2种指示剂,建立Ames波动试验的方法。Dexon采用0.1、1和10 μg/mL,SA采用0.01、0.1、1 μg/mL在非活化条件下与相应的溶剂对照进行试验;CP采用10、100、1 000 μg/mL,2-AF采用0.1、1和10 μg/mL在活化条件下与相应的溶剂对照进行试验;观察记录阳性孔数,根据情况调整阳性化合物的剂量,直到经统计分析后阳性孔数与溶剂对照组相比,差异有统计学意义(P<0.01)。确定各阳性化合物的剂量后,在相同剂量下重复试验3次,保证试验系统稳定可靠。结果:确定了Ames波动试验4种阳性化合物的剂量。在不加S9代谢活化系统的条件下,Dexon 3 μg/mL和SA 0.05 μg/mL,3块平行96孔板与溶剂对照组相比差异均有统计学意义(P<0.01),对TA100呈现出强致突变作用;在加入S9代谢活化系统的条件下,CP 100 μg/mL和2-AF 30 μg/mL,3块平行96孔板与溶剂对照组相比差异均有统计学意义(P<0.01),对TA100也呈现出强致突变作用。同时,在实验过程中改进了试验方法:包括对受试物剂量的标准化,改进了增菌培养的方法,并确定了指示剂。结论:建立了Ames波动试验方法,对已知阳性化合物测定结果的稳定性良好,并在研究中优化了实验条件。

关键词: Ames波动试验, 诱变试验, 标准化, 遗传毒性

Abstract:

OBJECTIVE: We developed a standard Ames fluctuation test in our laboratory and lay the foundation for its application in detecting the genetic toxicity of compounds. METHODS:We used four positive compounds in the test,Dexon,SA,CP and 2-AF. We compared two ways of enrichment culture and two indicators to eatablish the sandand percedure. We adopted 0.1,1,10 μg/mL Dexon and 0.01,0.1,1 μg/mL SA in the non-activated condition with their menstruum as negative control;10,100,1 000 μg/mL CP and 0.1,1,10 μg/mL 2-AF in the activated condition with their menstruum as negative control. We recorded the number of positive wells,adjusting the dose of the positive compounds accordingly,until there was a significant difference (P<0.01) between the positive group and the solvent compared group. After determining the dose of the positive control compounds,we repeated the test at the same dose 3 times,to ensure that the test system was stable and reliable. RESULTS:We determined the doses of the four positive compounds for the Ames fluctuation test in our laboratory,Dexon 3 μg/mL,SA 0.05 μg/mL,CP 100 μg/mL and 2-AF 30 μg/mL. In the non-activated condition 3 μg/mL Dexon and 0.05 μg/mL SA of the 3 96-well plates were significantly different from the solvent control group,exhibiting strong mutagenic effect to the TA100(P<0.01). Similarly,100 μg/mL CP and 30 μg/mL 2-AF in the activated condition of the 3 96-well plates were significantly different from the solvent control group,also showing strong mutagenic effect to the TA100(P<0.01). We also improved the test method during the experiment,including sandardizing the doses of test substance,improving enrichment culture method and determining the indicator. CONCLUSION:We established the Ames fluctuation test in our laboratory,confirmed that the known positive compounds were good and stable,and we optimized the experimental conditions in the study.

Key words: Ames fluctuation test, mutagenicity test, standardization, genetic toxicity