首页> 外文期刊>The Journal of toxicological sciences >Perfluorooctanoic acid (PFOA) but not perfluorooctane sulfonate (PFOS) showed DNA damage in comet assay on Paramecium caudatum.
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Perfluorooctanoic acid (PFOA) but not perfluorooctane sulfonate (PFOS) showed DNA damage in comet assay on Paramecium caudatum.

机译:在尾草履虫上的彗星试验中,全氟辛酸(PFOA)而不是全氟辛烷磺酸(PFOS)显示出DNA损伤。

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摘要

Persistent perfluorinated organic compounds such as perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) are distributed widely in the global environment including wildlife and human. In this study, we investigated the genotoxicity of PFOS and PFOA using the novel in vivo comet assay developed for Paramecium caudatum. For the comet assay, large nuclei squeezed out of the paramecia with 0.25 M sucrose containing 0.6% Triton X-100 were embedded in a layer of agarose gel placed over the slide glass. N-methyl-N -nitro-N-nitrosoguanidine (MNNG) and 2-aminoanthracene (2-AA) were successfully used for positive controls. Productions of 8-hydroxydeoxyguanosine (8-OH-dG) and intracellular reactive oxygen species (ROS) were also measured in paramecia. PFOS did not cause DNA damage on any conditions examined. On the other hand, 12 and 24 hr exposure to PFOA (100 microM) increased DNA migration in electrophoresis condition at pH 13, but not at pH 12.1, suggesting that the DNA damage may be alkali labile site (such as apurinic/apyrimidinic (AP) site). Exposure of paramecia to 100 microM PFOA for 1, 3 and 24 hr and to 10 microM PFOA for 24 hr significantly increased intracellular ROS. Under the same condition, however, 8-OH-dG level was not affected by PFOA. The PFOA-induced DNA damage was not abolished by the application of 100 microM GSH which completely inhibited the increase of intracellular ROS. In conclusion, the PFOA-induced in vivo DNA damage was first shown in paramecia, and the DNA damage might not be directly attributable to increase in intracellular ROS.
机译:持久性全氟有机化合物,例如全氟辛烷磺酸盐(PFOS)和全氟辛酸(PFOA)在包括野生生物和人类在内的全球环境中广泛分布。在这项研究中,我们使用为尾草履虫开发的新型体内彗星试验研究了PFOS和PFOA的遗传毒性。对于彗星试验,将用0.25 M含0.6%Triton X-100的蔗糖从拟寄生虫中挤出的大核包埋在载玻片上方的琼脂糖凝胶层中。 N-甲基-N-硝基-N-亚硝基胍(MNNG)和2-氨基蒽(2-AA)已成功用于阳性对照。在草履虫中还测量了8-羟基脱氧鸟苷(8-OH-dG)和细胞内活性氧(ROS)的产生。在任何检查条件下,PFOS均不会引起DNA损伤。另一方面,在pH 13的电泳条件下,暴露于PFOA(100 microM)的12和24小时会增加DNA的迁移,但在pH 12.1的条件下则不会增加,这表明DNA的损伤可能是对碱不稳定的部位(如嘌呤/嘧啶(AP) )网站)。将草皮暴露于100 microM PFOA持续1、3和24 hr,暴露于10 microM PFOA 24小时,显着增加了细胞内ROS。然而,在相同条件下,8-OH-dG水平不受PFOA影响。通过应用100 microM GSH可以完全消除细胞内ROS的增加,从而消除了PFOA诱导的DNA损伤。总而言之,PFOA诱导的体内DNA损伤首先出现在草履虫中,并且DNA损伤可能不直接归因于细胞内ROS的增加。

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