...
首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Time course evaluation of N-nitrosodialkylamines-induced DNA alkylation and oxidation in liver of mosquito fish.
【24h】

Time course evaluation of N-nitrosodialkylamines-induced DNA alkylation and oxidation in liver of mosquito fish.

机译:蚊鱼肝脏中N-亚硝基二烷基胺诱导的DNA烷基化和氧化的时程评估。

获取原文
获取原文并翻译 | 示例
           

摘要

Here we simultaneously measured N7-alkylguanines and 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) in liver of small fish, respectively, to assess the time course of the formation and removal of alkylation and oxidative damage to DNA caused by N-nitrosodialkylamines. Mosquito fish (Gambusia affinis) were killed at various times during (4 days) and post-exposure (16 days) to N-nitrosodimethylamine (NDMA) and N-nitrosodiethylamine (NDEA) alone or their combination with concentrations of 10 and 50mg/l. The modified guanine adducts were sensitively and selectively quantitated by isotope-dilution LC-MS/MS methods. During exposure, N7-methylguanine (N7-MeG) and N7-ethylguanine (N7-EtG) in liver DNA increased with the duration and dose of N-nitrosodialkylamine exposure, while 8-oxodG was dose-dependently induced within 1 day. It was found that NDMA formed substantially more N7-alkylated guanines and 8-oxodG than NDEA on the basis of adducts formed per micromolar concentration, suggesting that NDMA can be moreeasily bioactivated than NDEA to form reactive alkylating agents with the concomitant formation of oxygen radicals. After cessation of exposure, N7-alkylguanines remained elevated for 1 day and then gradually decreased over time but still higher than the background levels, even at day 16 (half-lives of 7-8 days). However, 8-oxodG was excised quickly from liver DNA and returned to the background level within 4 days post-exposure (half-lives less than 2 days). Taken together, this study firstly demonstrated that in addition to alkylation, N-nitrosodialkylamines can concurrently cause oxidative damage to DNA in vivo.
机译:在这里,我们同时测量了小鱼肝脏中的N7-烷基鸟嘌呤和8-oxo-7,8-二氢-2'-脱氧鸟嘌呤(8-oxodG),以评估烷基化和氧化损伤形成和消除的时间过程。由N-亚硝基二烷基胺引起的DNA在单独的N-亚硝基二甲胺(NDMA)和N-亚硝基二乙胺(NDEA)或浓度为10和50mg / l的组合中,蚊鱼(Gambusia affinis)在不同时间(4天)和暴露后(16天)被杀死。修饰的鸟嘌呤加合物通过同位素稀释LC-MS / MS方法灵敏且选择性地定量。在暴露过程中,肝脏DNA中的N7-甲基鸟嘌呤(N7-MeG)和N7-乙基鸟嘌呤(N7-EtG)随着N-亚硝基二烷基胺暴露的持续时间和剂量的增加而增加,而8-oxodG在1天内被剂量依赖地诱导。已经发现,基于每微摩尔浓度形成的加合物,NDMA比NDEA形成的N7-烷基化的鸟嘌呤和8-oxodG要多得多,这表明NDMA比NDEA可以更容易地被生物活化以形成反应性烷基化剂,并伴随有氧自由基的形成。停止接触后,N7-烷基鸟嘌呤保持升高1天,然后随时间逐渐降低,但仍高于本底水平,甚至在第16天(半衰期为7-8天)。但是,从肝脏DNA中快速切除了8-oxodG,并在暴露后4天内(半衰期少于2天)恢复到背景水平。两者合计,这项研究首先证明,除了烷基化,N-亚硝基二烷基胺还可以同时在体内引起DNA的氧化损伤。

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