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在果蝇体内不同纳米尺寸的二氧化硅纳米颗粒的遗传毒性效应。

In vivo genotoxic effects of four different nano-sizes forms of silica nanoparticles in Drosophila melanogaster.

机构信息

Akdeniz University, Faculty of Sciences, Department of Biology, 07058-Campus Antalya, Turkey.

Grup de Mutagènesi, Departament de Genètica i de Microbiologia, Facultat de Biociències, Universitat Autònoma de Barcelona, Campus de Bellaterra, Cerdanyola del Vallès, 08193 Barcelona, Spain; CIBER Epidemiología y Salud Pública, ISCIII, Madrid, Spain.

出版信息

J Hazard Mater. 2015;283:260-6. doi: 10.1016/j.jhazmat.2014.09.029. Epub 2014 Sep 28.

Abstract

Although the use of synthetic amorphous silica (SAS) is steady increasing, scarce information exists on its potential health risk. In particular few and conflictive data exist on its genotoxicity. To fill in this gap we have used Drosophila melanogaster as in vivo model test organism to detect the genotoxic activity of different SAS with different primary sizes (6, 15, 30 and 55 nm). The wing-spot assay and the comet assay in larvae haemocytes were used, and the obtained results were compared with those obtained with the microparticulated form (silicon dioxide). All compounds were administered to third instar larvae at concentrations ranging from 0.1 to 10mM. No significant increases in the frequencies of mutant spots were observed in the wing-spot assay with any of the tested compounds. On the other hand, significant dose-dependent increases in the levels of primary DNA damage, measured by the comet assay, were observed for all the SAS evaluated but mainly when high doses (5 and 10mM) were used. These in vivo results contribute to increase the database dealing with the potential genotoxic risk associated to SAS nanoparticles exposure.

摘要

尽管合成无定形二氧化硅 (SAS) 的使用稳步增加,但关于其潜在健康风险的信息却很少。特别是关于其遗传毒性的数据很少且存在冲突。为了填补这一空白,我们使用黑腹果蝇作为体内模型测试生物,以检测不同初级粒径(6、15、30 和 55nm)的不同 SAS 的遗传毒性活性。使用幼虫血细胞中的翅斑试验和彗星试验进行了检测,并将获得的结果与微颗粒形式(二氧化硅)的结果进行了比较。所有化合物均以 0.1 至 10mM 的浓度施用于三龄幼虫。在用任何测试化合物进行的翅斑试验中,均未观察到突变斑频率的显著增加。另一方面,在用彗星试验测量初级 DNA 损伤水平时,所有评估的 SAS 均观察到显著的剂量依赖性增加,但主要是在使用高剂量(5 和 10mM)时。这些体内结果有助于增加与 SAS 纳米颗粒暴露相关的潜在遗传毒性风险的数据库。

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