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马思佳, 霍娇, 陈锦瑶等. 大鼠体内Pig-a基因突变试验的优化及ENU时-效关系和 量-效关系评估[J]. 四川大学学报(医学版), 2017, 48(1): 127-131.
引用本文: 马思佳, 霍娇, 陈锦瑶等. 大鼠体内Pig-a基因突变试验的优化及ENU时-效关系和 量-效关系评估[J]. 四川大学学报(医学版), 2017, 48(1): 127-131.

大鼠体内Pig-a基因突变试验的优化及ENU时-效关系和 量-效关系评估

  • 摘要: 目的 对大鼠Pig-a基因突变试验方法进行优化,并初步探讨阳性诱变剂N-乙基-N-亚硝基脲(ENU)在该实验中的时-效关系和量-效关系。方法 30只雄性SD大鼠随机平均分为5组,即溶剂对照组,ENU 10 mg/kg、20 mg/kg、40 mg/kg和80 mg/kg 4个剂量组,连续3 d经口灌胃染毒。分别于实验第0、15、30、45、60、75、90天尾静脉取血,分离红细胞,经Anti-CD59-APC和SYTO 13核酸染料标记后采用流式细胞仪分析CD59表型突变为成熟红细胞(RBCCD59-)率、CD59表型突变为网织红细胞(RETCD59-)率以及RET占总红细胞百分率。结果 ENU各组大鼠在染毒后第15~90天的RBCCD59-率呈现随时间和剂量反应性地增高。RETCD59-率随时间延长,ENU各组表现为先增后基本稳定伴小幅波动趋势,但均保持在较高水平,在染毒后30 d出现最高峰,在45 d时出现下降;同时,随着ENU剂量的增加,ENU各组RETCD59-率也随之增加。随时间延长,ENU各组大鼠RET百分率有所下降,30 d后呈现较为稳定的轻微波动,5组间RET%在各时间点处差异均无统计学意义。结论 本研究改良的大鼠Pig-a基因突变试验可进行快速检测,ENU短期(3 d)染毒诱导大鼠红细胞Pig-a基因突变具有时-效关系和量-效关系。

     

    Abstract: Objective To optimize the method of Pig-a mutation assay, and to explore the time-dependent and dose-response relationship of N-ethyl-N-nitrosourea (ENU). Methods Thirty rats were randomly assigned to 5 groups: treated with PBS (control group)or different doses of ENU (10, 20, 40 and 80 mg/kg) for 3 d by oral gavage. Blood samples were collected at 0 d, 15 d, 30 d, 45 d, 60 d, 75 d and 90 d. After enrichment, erythrocytes were incubated with Anti-CD59-APC and SYTO 13 nucleic acid dye solution. Mutant phenotype erythrocytes (RBCCD59-) and mutant phenotype reticulocytes (RETCD59-) were measured by flow cytometry to analyze mutant frequencies, and the RET percentage was determined as well. Results The RBCCD59- mutation frequency in 4 ENU groups were significantly increased in a dose- and time-dependent manner. The RETCD59- mutation frequency increased to a stable high level with a slight fluctuation,and decreased at 45 d , with the peak values observed at 30 d. The RETCD59- mutation frequency showed a dose-dependent trend in 4 ENU groups. The RET percentage in all 5 groups declined at 30 d, to a stable low level thereafter, but the trends showed no significant differences by time or group. Conclusion The optimized in vivo Pig-a mutation assay could detecte the mutagen, such as ENU, induces mutation in RBC in a time- and dose-dependent manner.

     

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