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Inhibition of the formation of benzo[a]pyrene adducts to DNA in A549 lung cells exposed to mixtures of polycyclic aromatic hydrocarbons

机译:在暴露于多环芳烃混合物的A549肺细胞中抑制DNA生成苯并[a] to加合物

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摘要

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants, which exhibit carcinogenic properties especially in lungs. In the present work, we studied the effect of mixtures of 12 PAHs on the A549 alveolar cells. We first assess the ability of each PAH at inducing gene expression of phase I metabolization enzymes and at generating DNA adducts. A good correlation was found between these two endpoints. We then exposed cells to either binary mixtures of the highly genotoxic benzo[a]pyrene (B[a]P) with each PAH or complex mixtures of all studied PAHs mimicking by real emissions including combustion of wood, cigarette smoke, and atmospheres of garage, silicon factory and urban environments. Compared to pure B[a]P, both types of mixtures led to reduced CYP450 activity measured by the EROD test A similar trend was observed for the formation of DNA adducts. Surprisingly, the complex mixtures were more potent than B[a]P used at the same concentration for the induction of genes coding for CYP. Our results stress the lack of additivity of the genotoxic properties of PAH in mixtures. Interestingly, an opposite synergy in the formation of B[a]P adducts were observed previously in hepatocytes. Our data also show that measurement of the metabolic activity rather than quantification of gene expression reflects the actual bioactivation of PAHs into DNA damaging species. (C) 2016 Elsevier Ltd. All rights reserved.
机译:多环芳烃(PAHs)是普遍存在的污染物,尤其在肺部具有致癌性。在目前的工作中,我们研究了12种PAHs混合物对A549肺泡细胞的影响。我们首先评估每个PAH诱导I期代谢酶的基因表达以及产生DNA加合物的能力。在这两个端点之间发现了良好的相关性。然后,我们将细胞暴露于具有高遗传毒性的苯并[a] re(B [a] P)与每个PAH的二元混合物或所有研究的PAH的复杂混合物中,这些混合物模仿的是真实排放,包括燃烧木材,香烟烟雾和车库气氛,硅工厂和城市环境。与纯B [a] P相比,两种类型的混合物均导致通过EROD测试测得的CYP450活性降低。观察到类似的趋势,即DNA加合物的形成。出乎意料的是,复杂混合物比在相同浓度下用于诱导CYP编码基因的B [a] P更有效。我们的结果强调了混合物中PAH的遗传毒性特性缺乏可加性。有趣的是,先前在肝细胞中观察到了B [a] P加合物形成的相反协同作用。我们的数据还表明,对代谢活性的测量而不是基因表达的定量反映了PAHs实际生物激活成为DNA破坏物种的事实。 (C)2016 Elsevier Ltd.保留所有权利。

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