首页> 外文会议>Conference on Environmental Toxicology >Acute sublethal effects of 2,4,6-trinitrotoluene (TNT) on the European t A Anguilla anguilla (Linnaeus, 1758)
【24h】

Acute sublethal effects of 2,4,6-trinitrotoluene (TNT) on the European t A Anguilla anguilla (Linnaeus, 1758)

机译:2,4,6-三硝基甲苯(TNT)对欧洲T A Anguilla Anguilla(Linnaeus,1758)的急性核对效应

获取原文

摘要

The aim of this study is to investigate the effects of the explosive 2,4,6-trinitrotoluene (TNT) on liver phase I and II biotransformation enzymes at gene (CYP1A1, GST and UDPGT) and catalytic levels by investigating EROD, GST and UDPGT activities, on crucial brain steroidogenic proteins (StAR and P450scc genes expression) and on gills histology in a model fish species such as the European eel {Anguilla anguilla, Linnaeus, 1758). Eels were exposed in vivo for 6 and 24 hours to 0.5mg/L, 1mg/L and 2.5mg/L nominal concentration of TNT by using 0.1‰ of DMSO as a carrier. The TNT produced a significant inhibition of EROD activity and an increase of UDPG T and GST genes expression and activities compared to controls. A decrease of StAR and P450scc genes was also observed in TNT exposed eels. Finally concerning gills, branchial lifting was evident at the lowest TNT concentration (0.5 mg/L) while lamellar aneurisms, vascular congestion, hypertrophy and hyperplasia of the epithelium were evident at 2.5 mg/L. Our results highlighted the concern related to the release of TNT on the seabed: the inhibition of EROD activity may result in an increased susceptibility of the organism to P450 inducers such as dioxins and PAH. TNT also seems to affect fish neurosteroidogenesis by downregulating key enzymes (StAR and P450scc genes). Gills seem to be a target organ for TNT in fish. The present research provided relevant information on TNT metabolism/toxicity and indicated sensitive targets of TNT toxicity in fish species.
机译:本研究的目的是通过研究Erod,GST和UDPGT来研究爆炸性的2,4,6-三硝基甲苯(TNT)对基因(CYP1A1,GST和UDPGT)和催化水平的肝脏相I和II生物转化酶的影响在欧洲鳗鱼的模型鱼种中,在关键脑穗类蛋白(星级和P450SCC基因表达)和鳃组织中的活动,如欧洲鳗鱼{安圭拉安圭拉,Linnaeus,1758)。通过使用0.1‰作为载体,通过使用0.1‰作为载体将ELS暴露在体内6和24小时至0.5mg / L,1mg / L和2.5mg / L标称浓度。与对照相比,TNT产生了对EROD活性的显着抑制和UDPG T和GST基因的表达和活性。在TNT暴露的鳗中也观察到明星和P450SCC基因的减少。最后关于鳃,鳃升降在最低TNT浓度(0.5 mg / L)中明显明显,而上皮的层状动力学,血管性充血,肥大和增生是明显的2.5mg / L.我们的结果强调了与海底TNT释放有关的关切:EROD活性的抑制可能导致生物体对P450诱导剂的易感性增加,例如二恶英和PAH。 TNT似乎也通过下调关键酶(星和P450SCC基因)来影响鱼神经剂体系。吉尔斯似乎是鱼类的目标器官。本研究提供了有关TNT代谢/毒性的相关信息,并表明鱼类中TNT毒性的敏感靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
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