王宁, 张文众, 孙宇立, 邵乃敏, 成雪晴, 刘君丽, 丁瑜, 孙拿拿, 洪新宇. 大鼠体内肝细胞碱性彗星试验评估3种参考化学物的遗传毒性[J]. 上海预防医学, 2021, 33(7): 624-629. DOI: 10.19428/j.cnki.sjpm.2021.19610
引用本文: 王宁, 张文众, 孙宇立, 邵乃敏, 成雪晴, 刘君丽, 丁瑜, 孙拿拿, 洪新宇. 大鼠体内肝细胞碱性彗星试验评估3种参考化学物的遗传毒性[J]. 上海预防医学, 2021, 33(7): 624-629. DOI: 10.19428/j.cnki.sjpm.2021.19610
WANG Ning, ZHANG Wen-zhong, SUN Yu-li, SHAO Nai-min, CHENG Xue-qing, LIU Jun-li, DING Yu, SUN Na-na, HONG Xin-yu. Genotoxicity assessment of three reference chemicals in rat hepatocytes by alkaline comet assay[J]. Shanghai Journal of Preventive Medicine, 2021, 33(7): 624-629. DOI: 10.19428/j.cnki.sjpm.2021.19610
Citation: WANG Ning, ZHANG Wen-zhong, SUN Yu-li, SHAO Nai-min, CHENG Xue-qing, LIU Jun-li, DING Yu, SUN Na-na, HONG Xin-yu. Genotoxicity assessment of three reference chemicals in rat hepatocytes by alkaline comet assay[J]. Shanghai Journal of Preventive Medicine, 2021, 33(7): 624-629. DOI: 10.19428/j.cnki.sjpm.2021.19610

大鼠体内肝细胞碱性彗星试验评估3种参考化学物的遗传毒性

Genotoxicity assessment of three reference chemicals in rat hepatocytes by alkaline comet assay

  • 摘要:
    目的建立大鼠体内肝细胞碱性彗星试验方法,检测3种参考化学物的遗传毒性。
    方法将6~10周龄的Sprague Dawley大鼠随机分为4组,每组10只,雌雄各半。以生理盐水(0.9% NaCl溶液)为阴性对照组,受试物组分为甲基磺酸乙酯(EMS)200 mg/kg组、N-甲基-N-亚硝基脲(MNU)50 mg/kg组和D-甘露醇2 000 mg/kg组。连续2次(间隔21 h)灌胃染毒,实验期间记录动物临床症状和体质量变化。末次染毒3 h后处死大鼠,称量肝脏重量,取肝脏制备单细胞悬液开展肝细胞碱性彗星试验,测定肝细胞平均尾部DNA含量百分比(DNA%)等指标。
    结果受试物EMS、MNU和D-甘露醇均未对动物整体产生严重的毒性作用。与阴性对照组大鼠肝细胞平均尾部DNA含量百分比[(2.32±1.39)%]相比,EMS和MNU组分别为(60.07±24.69)%和(41.66±22.35)%,差异有统计学意义(P<0.05);D-甘露醇组差异无统计学意义[(3.06±3.30)%,P>0.05]。
    结论本实验室初步建立了大鼠体内肝细胞碱性彗星试验方法,3种参考化学物质中,EMS和MNU有明显遗传毒性,D-甘露醇组未见遗传毒性。

     

    Abstract:
    ObjectiveTo establish a comet test method for detection of genotoxicity of three reference chemicals in rat liver cells.
    Methods6-10 week old Sprague Dawley rats were randomly divided into 4 groups, with normal saline (0.9% NaCl solution) as negative control group. Animals in three test groups were treated, respectively, with ethyl methanesulfonate (EMS) 200 mg/kg, N-methyl-N-nitrosourea (MNU) 50 mg/kg, and D-mannitol 2 000 mg/kg. There were 10 animals in each group, 5 males and 5 females. The animals received two times (21 h interval) of test compounds through intragastric administration, and their clinical symptoms and body weight changes were recorded during the experiment. The rats were sacrificed 3 h after the last exposure. The liver was weighed, then used to prepare single-cell suspensions for the alkaline comet test which determines the average tail DNA content percentage (DNA%) of hepatocytes and other comet indicators.
    Results(1) D-mannitol, EMS and MNU did not show significant toxicity in the whole animal. (2) The mean values of tail DNA content percentage (DNA%) of rat hepatocytes in EMS [(60.07±24.69)%] and MNU [(41.66±22.35)%] groups were higher than that in the negative control group [(2.32±1.39)%] and the difference was statistically significant (P<0.05). The difference between D-mannitol group [(3.06±3.30)%] and the negative control group was not significant (P>0.05).
    ConclusionThis laboratory has established a comet test method using hepatocytes from treated rats. Among three testing chemicals, EMS and MNU have displayed genotoxicity by this assay, but no genotoxicity was observed in D-mannitol treated animals.

     

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