首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Hematite (Fe(2)O(3)) enhances benzo(a)pyrene genotoxicity in endotracheally treated rat, as determined by Comet Assay.
【24h】

Hematite (Fe(2)O(3)) enhances benzo(a)pyrene genotoxicity in endotracheally treated rat, as determined by Comet Assay.

机译:赤铁矿(Fe(2)O(3))增强气管内治疗大鼠的苯并(a)re遗传毒性,由彗星试验确定。

获取原文
获取原文并翻译 | 示例
           

摘要

Since epidemiological studies have firmly implied the co-exposition between iron oxides and polycyclic aromatic hydrocarbons (PAH) as potential etiological factor involved in the excess of mortality by lung cancer in miners, experimental studies have been performed to investigate the role of iron particles on benzo[a]pyrene (B[a]P)-induced lung pathogenesis. In the present study, the alkaline single-cell gel electrophoresis (SCGE; Comet Assay) was used to measure DNA single-strand breaks in four cell types (alveolar macrophages, lung cells, peripheral lymphocytes and hepatocytes) of OFA Sprague-Dawley rats 24h after endotracheal administration of a single dose of an iron oxide (hematite; Fe(2)O(3)) (0.75mg) or B[a]P (0.75mg) or B[a]P (0.75mg) coated onto hematite particles (0.75mg). No damage was observed in cell from the four investigated organs in rats treated with iron oxide alone, while a statistically significant increase in DNA damage was observed compared with control animals in all tested cell types of rats treated with B[a]P alone or in association with hematite. The highest levels of damage were observed in lung cells and peripheral lymphocytes; the levels of damage in alveolar macrophages and hepatocytes were increased, but to a lesser extent compared with the first two cell types.The main finding was to notice a statistically significant increase of the damage in all organs of rats treated with B[a]P coated onto hematite (approximately two-fold increases; P<0.001), versus B[a]P alone. The current study shows that iron particles increase the genotoxic properties of B[a]P in the respiratory tract of endotracheally treated OFA Sprague-Dawley rats. Hence, our data may contribute to explain the excess mortality by lung cancer in epidemiological studies and overall why exposures to B[a]P coated onto Fe(2)O(3) particles resulted in higher toxicity in rodents compared with exposure to B[a]P alone.
机译:由于流行病学研究已明确暗示铁氧化物与多环芳烃(PAH)的共暴露是矿工肺癌过度死亡的潜在病因,因此进行了实验研究以研究铁颗粒在苯并中的作用[a] py(B [a] P)诱导的肺部发病机理。在本研究中,碱性单细胞凝胶电泳(SCGE;彗星分析)用于测量OFA Sprague-Dawley大鼠24h的四种细胞类型(肺泡巨噬细胞,肺细胞,外周淋巴细胞和肝细胞)中的DNA单链断裂气管内施用单剂量的氧化铁(赤铁矿; Fe(2)O(3))(0.75mg)或B [a] P(0.75mg)或B [a] P(0.75mg)涂覆在赤铁矿上后颗粒(0.75mg)。在单独用氧化铁处理的大鼠的所有测试细胞类型中,与单独使用氧化铁处理的大鼠相比,在四个受调查器官的细胞中均未观察到损伤,而与对照组相比,DNA损伤的统计学显着增加与赤铁矿有关。在肺细胞和外周淋巴细胞中观察到最高的损伤水平。与前两种细胞类型相比,肺泡巨噬细胞和肝细胞的损伤程度有所增加,但程度较小。主要发现是,在用B [a] P处理的大鼠中,所有器官的损伤均具有统计学意义与单独的B [a] P相比,将其涂覆在赤铁矿上(大约增加了两倍; P <0.001)。目前的研究表明,铁颗粒可提高经气管内治疗的OFA Sprague-Dawley大鼠呼吸道中B [a] P的遗传毒性。因此,我们的数据可能有助于解释流行病学研究中肺癌造成的过高死亡率,以及总体而言,为什么暴露于涂在Fe(2)O(3)颗粒上的B [a] P与暴露于B [一个] P。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号