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全氟辛酸(PFOA)而非全氟辛烷磺酸(PFOS)在草履虫彗星试验中显示出 DNA 损伤。

Perfluorooctanoic acid (PFOA) but not perfluorooctane sulfonate (PFOS) showed DNA damage in comet assay on Paramecium caudatum.

机构信息

Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Japan.

出版信息

J Toxicol Sci. 2010 Dec;35(6):835-41. doi: 10.2131/jts.35.835.

Abstract

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 µM) 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 µM PFOA for 1, 3 and 24 hr and to 10 µM 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 µM 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.

摘要

持久性全氟有机化合物,如全氟辛烷磺酸 (PFOS) 和全氟辛酸 (PFOA),广泛分布于包括野生动物和人类在内的全球环境中。在这项研究中,我们使用为草履虫开发的新型体内彗星试验来研究 PFOS 和 PFOA 的遗传毒性。对于彗星试验,用 0.25 M 蔗糖和 0.6% Triton X-100 挤出的大核被嵌入放在载玻片上的琼脂糖凝胶层中。N-甲基-N´-硝基-N-亚硝基胍 (MNNG) 和 2-氨基蒽 (2-AA) 成功地用作阳性对照。也在草履虫中测量了 8-羟基脱氧鸟苷 (8-OH-dG) 和细胞内活性氧 (ROS) 的产生。在检查的任何条件下,PFOS 均未引起 DNA 损伤。另一方面,12 和 24 小时暴露于 100 µM 的 PFOA 会增加电泳条件下 pH 值为 13 时的 DNA 迁移,但 pH 值为 12.1 时不会,这表明 DNA 损伤可能是碱不稳定部位(如无嘌呤/无嘧啶 (AP) 部位)。暴露于 100 µM PFOA 1、3 和 24 小时以及 10 µM PFOA 24 小时后,草履虫的细胞内 ROS 显著增加。然而,在相同条件下,PFOA 并未影响 8-OH-dG 水平。100 µM GSH 的应用并未消除 PFOA 诱导的 DNA 损伤,GSH 完全抑制了细胞内 ROS 的增加。总之,首次在草履虫中显示了 PFOA 诱导的体内 DNA 损伤,并且 DNA 损伤可能与细胞内 ROS 的增加没有直接关系。

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