Abstract Comparative live-imaging of in vivo EROD (ethoxyresorufin-O-deethylase) induction in zebrafish (Danio rerio) and fathead minnow (Pimephales promelas) embryos after exposure to PAHs and river sediment extracts
首页> 外文期刊>The Science of the Total Environment >Comparative live-imaging of in vivo EROD (ethoxyresorufin-O-deethylase) induction in zebrafish (Danio rerio) and fathead minnow (Pimephales promelas) embryos after exposure to PAHs and river sediment extracts
【24h】

Comparative live-imaging of in vivo EROD (ethoxyresorufin-O-deethylase) induction in zebrafish (Danio rerio) and fathead minnow (Pimephales promelas) embryos after exposure to PAHs and river sediment extracts

机译:暴露于PAHs和河底沉积物提取物后斑马鱼(Danio rerio)和黑头now鱼(Pimephales promelas)胚胎体内EROD(乙氧基-异色蛋白-O-脱乙基酶)诱导的活体成像比较

获取原文
获取原文并翻译 | 示例
           

摘要

AbstractThe measurement of EROD (ethoxyresorufin-O-deethylase) activity to determine the induction of CYP1A after exposure to dioxin-like substances is a well-established biomarker in fish. For reasons of animal welfare and implementations of new chemicals regulations (REACh),in vivomethods using zebrafish (Danio rerio) and medaka (Oryzias latipes) embryos have recently been developed to quantify CYP1A induction, which is visualized as mean intensity of the autofluorescent resorufin formed in living anaesthetized embryos.In the present study, concentration ranges of three PAHs (benzo[a]pyrene, β-naphthoflavone, benzo[k]fluoranthene) as examples of known CYP1A inducers as well as extracts of two well-characterized sediment samples of the lower Neckar river (Southern Germany) were used to determine the suitability of the fathead minnow (Pimephales promelas) embryo for thein vivoEROD assay. Data for zebrafish embryos were generated for comparison. Fathead minnow embryos were principally suitable to showin vivoEROD inductionvialive-imaging. Since in fathead minnow embryos both signal area and fluorescence intensities are lower than in zebrafish embryos, the induction potentials of the three model PAHs and the environmental samples proved to be species-dependent.Among the three PAHs tested, benzo[k]fluoranthene lead to the strongest EROD signal followed by β-naphthoflavone and benzo[a]pyrene in comparison to the positive control. Whereas benzo[k]fluoranthene and β-naphthoflavone showed a dose-response relationship for the EROD induction, benzo[a]pyrene failed to induce a significant signal in fathead minnow embryos. If compared to the model PAHs, the extracts of both sediments from the lower Neckar River induced stronger EROD signals in both fathead minnow and zebrafish embryos. Observations thus documented fathead minnow embryos to be as suitable for biomonitoring purposes as are zebrafish embryos.Graphical abstractDisplay OmittedHighlightsFathead minnow embryos are suitable to showin vivoEROD inductionvialive-imaging.EROD signal intensities in the fathead minnow are lower compared to zebrafish.Induction potential of tested PAHs and environmental samples is species-dependent.EROD signal intensities: benzo[k]fluoranthene>β-naphthoflavone>benzo[a]pyrene.Environmental samples induced stronger EROD signals compared with PAHs.
机译: 摘要 通过测量EROD(乙氧基间苯二酚- O -脱乙基酶)活性来确定诱导暴露于二恶英样物质后,CYP1A是鱼类中公认的生物标志物。出于动物福利和实施新化学品法规(REACh)的原因,在体内使用斑马鱼( Danio rerio )和medaka( ce:italic> 方法ce:italic> Oryzias latipes )胚胎最近被用来量化CYP1A诱导作用,可视化为在活着的麻醉胚胎中形成的自发荧光试卤灵的平均强度。 在本研究中,三种PAH(苯并[β],萘黄酮,苯并[ k ]荧蒽)以及已知的CYP1A诱导剂实例以及内卡河下游(德国南部)两种特征鲜明的沉积物样品的提取物来确定the鱼head鱼的适宜性( Pimephales promelas )胚胎用于体内 EROD检测。产生斑马鱼胚胎的数据用于比较。胖头min鱼胚胎主要适于通过活体成像显示体内 EROD诱导。由于黑头head鱼胚胎的信号面积和荧光强度均低于斑马鱼胚胎,因此三种模式PAHs和环境样品的诱导电势均与物种有关。 在测试的三个PAH中,苯并[ k ]荧蒽导致最强的EROD信号,其次是β-萘黄酮和苯并[ a ] re与阳性对照相比。苯并[ k ]荧蒽和β-萘黄酮对EROD的诱导具有剂量-反应关系,而苯并[ a ] re没有在黑头min鱼胚胎中诱导明显的信号。如果与模型PAHs进行比较,则内卡河下游的两种沉积物的提取物在黑头fat鱼和斑马鱼的胚胎中都产生了更强的EROD信号。因此,观察结果证明,黑头min鱼胚胎与斑马鱼胚胎一样适合于生物监测。 图形摘要 省略显示 突出显示 肥头min鱼胚胎适合体内显示 ER OD诱导通过实时成像。 在黑头min鱼中的EROD信号强度低于斑马鱼。 测试的PAH和环境样品的诱导潜力取决于物种。 EROD信号强度:苯并[ k ]荧蒽>β-萘黄酮>苯并[ a ] py。 环境样本与多环芳烃相比,诱导的EROD信号更强。

著录项

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号