Universidade da Coruña, Grupo NanoToxGen, Centro Interdisciplinar de Química e Bioloxía-CICA, Departamento de Biología, Facultad de Ciencias, Campus A Zapateira s/n, 15071, A Coruña, Spain; Instituto de Investigación Biomédica de A Coruña (INIBIC), Complexo Hospitalario Universitario de A Coruña (CHUAC), Sergas, As Xubias, 15006, A Coruña, Spain.
Universidade da Coruña, Grupo NEUROVER, Centro Interdisciplinar de Química e Bioloxía-CICA, Rúa As Carballeiras, 15071, A Coruña, Spain.
Chemosphere. 2024 Sep;363:142993. doi: 10.1016/j.chemosphere.2024.142993. Epub 2024 Aug 2.
Due to their extensive use, the release of zinc oxide nanoparticles (ZnO NP) into the environment is increasing and may lead to unintended risk to both human health and ecosystems. Access of ZnO NP to the brain has been demonstrated, so their potential toxicity on the nervous system is a matter of particular concern. Although evaluation of ZnO NP toxicity has been reported in several previous studies, the specific effects on the nervous system are not completely understood and, particularly, effects on genetic material and on organism behaviour are poorly addressed. We evaluated the potential toxic effects of ZnO NP in vitro and in vivo, and the role of zinc ions (Zn) in these effects. In vitro, the ability of ZnO NP to be internalized by A172 glial cells was verified, and the cytotoxic and genotoxic effects of ZnO NP or the released Zn ions were addressed by means of vital dye exclusion and comet assay, respectively. In vivo, behavioural alterations were evaluated in zebrafish embryos using a total locomotion assay. ZnO NP induced decreases in viability of A172 cells after 24 h of exposure and genetic damage after 3 and 24 h. The involvement of the Zn ions released from the NP in genotoxicity was confirmed. ZnO NP exposure also resulted in decreased locomotor activity of zebrafish embryos, with a clear role of released Zn ions in this effect. These findings support the toxic potential of ZnO NP showing, for the first time, genetic effects on glial cells and proving the intervention of Zn ions.
由于氧化锌纳米粒子(ZnO NP)的广泛使用,其向环境中的释放量正在增加,这可能对人类健康和生态系统带来意想不到的风险。已经证明 ZnO NP 可以进入大脑,因此它们对神经系统的潜在毒性是一个特别值得关注的问题。尽管以前的几项研究已经评估了 ZnO NP 的毒性,但对神经系统的具体影响还不完全清楚,特别是对遗传物质和生物体行为的影响还没有得到很好的解决。我们评估了 ZnO NP 在体外和体内的潜在毒性作用,以及锌离子(Zn)在这些作用中的作用。在体外,验证了 ZnO NP 被 A172 神经胶质细胞内化的能力,并通过活染料排除和彗星试验分别研究了 ZnO NP 或释放的 Zn 离子的细胞毒性和遗传毒性作用。在体内,通过总运动试验评估了斑马鱼胚胎的行为改变。暴露 24 小时后,ZnO NP 降低了 A172 细胞的活力,暴露 3 和 24 小时后导致遗传损伤。证实了从 NP 释放的 Zn 离子在遗传毒性中的作用。ZnO NP 暴露还导致斑马鱼胚胎的运动活性降低,释放的 Zn 离子在这种作用中起明显作用。这些发现支持 ZnO NP 的毒性潜力,首次显示了对神经胶质细胞的遗传影响,并证明了 Zn 离子的干预作用。