Department of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina 27599, United States.
Chem Res Toxicol. 2012 Feb 20;25(2):391-9. doi: 10.1021/tx200447w. Epub 2012 Jan 24.
Vinyl chloride (VC) is an industrial chemical that is known to be carcinogenic to animals and humans. VC primarily induces hepatic angiosarcomas following high exposures (≥50 ppm). VC is also found in Superfund sites at ppb concentrations as a result of microbial metabolism of trichloroethylene and perchloroethylene. Here, we report a new sensitive LC-MS/MS method to analyze the major DNA adduct formed by VC, 7-(2-oxoethylguanine) (7-OEG). We used this method to analyze tissue DNA from both adult and weanling rats exposed to 1100 ppm [(13)C(2)]-VC for 5 days. After neutral thermal hydrolysis, 7-OEG was derivatized with O-t-butyl hydroxylamine to an oxime adduct, followed by LC-MS/MS analysis. The limit of detection was 1 fmol, and the limit of quantitation was 1.5 fmol on the column. The use of stable isotope VC allowed us to demonstrate for the first time that endogenous 7-OEG was present in tissue DNA. We hypothesized that endogenous 7-OEG was formed from lipid peroxidation and demonstrated the formation of [(13)C(2)]-7-OEG from the reaction of calf thymus DNA with [(13)C(18)]-ethyl linoleate (EtLa) under peroxidizing conditions. The concentrations of endogenous 7-OEG in liver, lung, kidney, spleen, testis, and brain DNA from adult and weanling rats typically ranged from 1.0 to 10.0 adducts per 10(6) guanine. The exogenous 7-OEG in liver DNA from adult rats exposed to 1100 ppm [(13)C(2)]-VC for 5 days was 104.0 ± 23.0 adducts per 10(6) guanine (n = 4), while concentrations in other tissues ranged from 1.0 to 39.0 adducts per 10(6) guanine (n = 4). Although endogenous concentrations of 7-OEG in tissues in weanling rats were similar to those of adult rats, exogenous [(13)C(2)]-7-OEG concentrations were higher in weanlings, averaging 300 adducts per 10(6) guanine in liver. Studies on the persistence of [(13)C(2)]-7-OEG in adult rats sacrificed 2, 4, and 8 weeks postexposure to [(13)C(2)]-VC demonstrated a half-life of 7-OEG of 4 days in both liver and lung.
氯乙烯 (VC) 是一种已知对动物和人类具有致癌性的工业化学物质。VC 主要在高暴露(≥50 ppm)下诱导肝血管肉瘤。由于三氯乙烯和全氯乙烯的微生物代谢,VC 也以 ppb 浓度存在于超级基金站点中。在这里,我们报告了一种新的灵敏 LC-MS/MS 方法来分析 VC 形成的主要 DNA 加合物,7-(2-氧代乙基鸟嘌呤) (7-OEG)。我们使用该方法分析了暴露于 1100 ppm [(13)C(2)]-VC 5 天的成年和断奶大鼠的组织 DNA。中性热水解后,7-OEG 用 O-叔丁基羟胺衍生化为肟加合物,然后进行 LC-MS/MS 分析。检测限为 1 fmol,柱上定量限为 1.5 fmol。使用稳定同位素 VC,我们首次证明内源性 7-OEG 存在于组织 DNA 中。我们假设内源性 7-OEG 是由脂质过氧化形成的,并证明了小牛胸腺 DNA 与过氧化条件下的 [(13)C18]-乙基亚油酸 (EtLa) 反应生成 [(13)C(2)]-7-OEG。成年和断奶大鼠肝、肺、肾、脾、睾丸和脑组织 DNA 中内源性 7-OEG 的浓度通常为 1.0 至 10.0 个加合物/10(6)鸟嘌呤。暴露于 1100 ppm [(13)C(2)]-VC 5 天的成年大鼠肝 DNA 中的外源性 7-OEG 为 104.0 ± 23.0 个加合物/10(6)鸟嘌呤(n = 4),而其他组织中的浓度范围为 1.0 至 39.0 个加合物/10(6)鸟嘌呤(n = 4)。尽管断奶大鼠组织中 7-OEG 的内源性浓度与成年大鼠相似,但外源性 [(13)C(2)]-7-OEG 浓度在断奶大鼠中更高,肝中平均每个 10(6)鸟嘌呤有 300 个加合物。对暴露于 [(13)C(2)]-VC 2、4 和 8 周后处死的成年大鼠中 [(13)C(2)]-7-OEG 持久性的研究表明,肝和肺中 7-OEG 的半衰期为 4 天。