Laboratory of Water, Biodiversity & Climate Change, Cadi Ayyad University, B.P. 2390, 40000, Marrakech, Morocco; National Centre for Studies and Research on Water and Energy (CNEREE), Cadi Ayyad University, B. P 511, 40000, Marrakech, Morocco; Laboratory of Clinical, Experimental and Environmental Neurosciences, Cadi Ayyad University, Marrakech, Morocco.
Laboratory of Clinical, Experimental and Environmental Neurosciences, Cadi Ayyad University, Marrakech, Morocco.
Food Chem Toxicol. 2023 Jan;171:113553. doi: 10.1016/j.fct.2022.113553. Epub 2022 Dec 12.
Graphene oxide (GO) is a graphene derivative used for numerous applications in which biomedical uses are significant. However, for this application, the security of GO is doubtful. In this work, we synthesized this nanoparticle to assess its toxicity in male mice. In addition, we studied the effects of this nanomaterial on behavior by administering GO intraperitoneally to mice at different doses (2 mg/kg and 5 mg/kg) for five days. Subsequently, we performed biochemical analyses of blood serum and measured peroxidase and malondialdehyde (MDA) activity. Then, we performed histological sections to evaluate the brain's and liver's pathological and morphological changes. The data showed that the open field tests did not alter the locomotor activity. Furthermore, the elevated cross-maze tests showed no anxiety effect in the GO doses in the animals. The biochemical analyses indicated that GO influenced the level of biochemical parameters. Although, the oxidative stress assay showed an increase in peroxidase and MDA activity after GO intoxication. However, histopathological analysis of liver sections showed that GO caused liver inflammation, whereas, at the brain level, GO did not affect neuronal cells. The results indicate that GO caused toxic effects and that its toxicity could be mediated by oxidative stress.
氧化石墨烯(GO)是一种石墨烯衍生物,用于许多应用中,其中生物医学用途非常重要。然而,对于这种应用,GO 的安全性值得怀疑。在这项工作中,我们合成了这种纳米颗粒,以评估其在雄性小鼠中的毒性。此外,我们通过向小鼠腹腔内给予不同剂量(2mg/kg 和 5mg/kg)的 GO 五天来研究这种纳米材料对行为的影响。随后,我们对血清进行了生化分析,并测量了过氧化物酶和丙二醛(MDA)的活性。然后,我们进行了脑组织和肝脏组织学切片,以评估其病理和形态变化。数据显示,旷场试验并未改变运动活性。此外,高架十字迷宫试验表明,在动物中,GO 剂量没有引起焦虑效应。生化分析表明,GO 影响了生化参数的水平。尽管如此,氧化应激检测表明 GO 中毒后过氧化物酶和 MDA 活性增加。然而,肝脏切片的组织病理学分析表明,GO 引起了肝脏炎症,而在大脑水平上,GO 未影响神经元细胞。结果表明,GO 引起了毒性作用,其毒性可能是通过氧化应激介导的。