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首页> 外文期刊>Archives of Toxicology >Evaluation of inhaled low-dose formaldehyde-induced DNA adducts and DNA-protein cross-links by liquid chromatography-tandem mass spectrometry
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Evaluation of inhaled low-dose formaldehyde-induced DNA adducts and DNA-protein cross-links by liquid chromatography-tandem mass spectrometry

机译:通过液相色谱 - 串联质谱法评价吸入的低剂量甲醛诱导的DNA加合物和DNA-蛋白的交联

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摘要

As a widespread industrial chemical, formaldehyde carcinogenicity has been highly controversial. Meanwhile, formaldehyde is an essential metabolite in all living cells. Previously, we have demonstrated exogenous formaldehyde causes DNA adducts in a nonlinear manner between 0.7 and 15.2 ppm using [(CD2)-C-13]-formaldehyde for exposure coupled with the use of sensitive mass spectrometry. However, the responses from exposure to low doses of formaldehyde are still unknown. In this study, rats were exposed to 1, 30, and 300 ppb [(CD2)-C-13]-formaldehyde for 28 days (6 h/day) by nose-only inhalation, followed by measuring DNA mono-adduct (N-2-HOMe-dG) and DNA-protein crosslinks (dG-Me-Cys) as formaldehyde specific biomarkers. Both exogenous and endogenous DNA mono-adducts and dG-Me-Cys were examined with ultrasensitive nano-liquid chromatography-tandem mass spectrometry. Our data clearly show that endogenous adducts are present in all tissues analyzed, but exogenous adducts were not detectable in any tissue samples, including the most susceptible nasal epithelium. Moreover, formaldehyde exposure at 1, 30 and 300 ppb did not alter the levels of endogenous formaldehyde-induced DNA adducts or DNA-protein crosslinks. The novel findings from this study provide new data for risk assessment of exposure to low doses of formaldehyde.
机译:作为广泛的工业化学品,甲醛致癌性具有高度争议性。同时,甲醛是所有活细胞中的必需代谢物。以前,我们已经证明外源性甲醛在0.7和15.2ppm的非线性方式中使用[(CD2)-C-13] - 甲醛与使用敏感质谱相连,使DNA加合物。然而,暴露于低剂量甲醛的反应仍然是未知的。在该研究中,通过仅鼻子吸入将大鼠暴露于1,300和300ppb [(CD2)-C-13] - 甲醛28天(6小时/天),然后测量DNA单加合物(n -2-home-dg)和DNA-蛋白交联(DG-ME-CYS)作为甲醛特异性生物标志物。用超细纳米液相色谱 - 串联质谱法检测外源性和内源性DNA单加合物和DG-ME-CYS。我们的数据清楚地表明,在分析的所有组织中存在内源性加合物,但在任何组织样本中都没有检测到外源性加合物,包括最易感的鼻上皮。此外,在1,30和300ppb下甲醛暴露未改变内源性甲醛诱导的DNA加合物或DNA蛋白交联水平。本研究的新发现提供了对低剂量甲醛暴露的风险评估的新数据。

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