钮利喜, 王萍, 朱欣凯, 陆颖冲, 赵美蓉. 氯菊酯异构体对人类绒毛膜癌JEG-3细胞内分泌的选择性干扰[J]. 农药学学报, 2016, 18(4): 431-438. DOI: 10.16801/j.issn.1008-7303.2016.0060
    引用本文: 钮利喜, 王萍, 朱欣凯, 陆颖冲, 赵美蓉. 氯菊酯异构体对人类绒毛膜癌JEG-3细胞内分泌的选择性干扰[J]. 农药学学报, 2016, 18(4): 431-438. DOI: 10.16801/j.issn.1008-7303.2016.0060
    NIU Lixi, WANG Ping, ZHU Xinkai, LU Yingchong, ZHAO Meirong. Endocrine disruption effect of permethrin isomers to the chorion carcinoma JEG-3 cells[J]. Chinese Journal of Pesticide Science, 2016, 18(4): 431-438. DOI: 10.16801/j.issn.1008-7303.2016.0060
    Citation: NIU Lixi, WANG Ping, ZHU Xinkai, LU Yingchong, ZHAO Meirong. Endocrine disruption effect of permethrin isomers to the chorion carcinoma JEG-3 cells[J]. Chinese Journal of Pesticide Science, 2016, 18(4): 431-438. DOI: 10.16801/j.issn.1008-7303.2016.0060

    氯菊酯异构体对人类绒毛膜癌JEG-3细胞内分泌的选择性干扰

    Endocrine disruption effect of permethrin isomers to the chorion carcinoma JEG-3 cells

    • 摘要: 以人类绒毛膜癌JEG-3细胞为模型,通过考察拟除虫菊酯类农药氯菊酯(permethrin,PM)及其异构体对JEG-3细胞内分泌相关基因的干扰情况,探讨了氯菊酯及其异构体暴露对产妇胎儿健康的潜在风险。通过高效液相色谱拆分得到氯菊酯的4个异构体,采用实时荧光定量反转录聚合酶链式反应(reverse transcription polymerase chain reaction,RT-PCR)法检测目的基因的相对表达水平,发现氯菊酯异构体对JEG-3细胞促性腺激素释放激素(GnRHI,GnRHⅡ)及其受体(GnRHR)、胆甾醇类雌激素合成关键基因以及胚胎免疫耐受相关基因(HLA-G)在mRNA水平的相对表达量均呈现选择性干扰,其中1R-cis-PM和1S-trans-PM对滋养层细胞内分泌相关基因表达量的影响大于其他2个异构体。

       

      Abstract: The endocrine disruption effect of four permethrin isomers to the chorion carcinoma JEG-3 cells was investigated. JEG-3 cell lines was employed as the in vitro model and the potential risks of these compounds to maternal-fetal health were also evaluated. Four permethrin isomers were separated by HPLC. The results of real-time reverse transcription polymerase chain reaction (RT-PCR) revealed that those four isomers, in RNA levels, exhibited selective influence on the relative expression amounts of the genes correspounding to gonadotropin-releasing hormone (GnRH) and its receptor, the enzymes of the steroidogenesis pathway and human leucocyte antigen G (HLA-G). The endocrine disruption effects induced by 1R-cis-PM and 1S-trans-PM were more significant than that induced by 1S-cis-PM and 1R-trans-PM.

       

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