1 Research Laboratory for Molecular Carcinogenesis, Department of Zoology, Faculty of Science, Tanta University, Tanta, Egypt.
2 Mammalian and Aquatic Toxicology Department, Central Agricultural Pesticides Laboratory, ARC, Dokki, Giza, Egypt.
Hum Exp Toxicol. 2019 Jun;38(6):734-745. doi: 10.1177/0960327119836199. Epub 2019 Apr 1.
A quantitative assessment of the genotoxicity of silver nanoparticles (AgNPs) ascribed to its transplacental transfer and tissue distribution in pregnant rats was carried out in this study. A single intravenous (i.v.) injection of AgNPs with a size range from 4.0 to 17.0 nm was administered to pregnant rats at a dose of 2 mg/kg b.w. on the 19th day of gestation. Five groups beside control, each of the five rats were euthanized after 10 min, 1, 6, 12, or 24 h, respectively. The accumulation of nanoparticles (NPs) in mother and fetal tissues was quantified by inductively coupled plasma optical emission spectroscopy, where the highest accumulation level was recorded in maternal blood (0.523 µg/ml) after 24 h of administration. AgNPs induced accumulation in spleen tissue higher than placenta and fetal tissue homogenates. The data showed significantly detected levels of 8-hydroxydeoxyguanosine in all collected samples from administered animals compared with untreated individuals. Level of 8-OHdG in amniotic fluid exhibited the greatest values followed by maternal spleen, kidneys, and liver, respectively. Investigation by transmission electron microscope showed that the transfer of AgNPs through placental wall caused indentation of nuclei, clumped chromatin, pyknotic nuclei, and focal necrotic areas, while AgNPs appeared mainly accumulated in the macrophages of the spleen. Therefore, the data assume that the genotoxicity studies of AgNPs must be recommended during a comprehensive assessment of the safety of novel types of NPs and nanomaterials. Additionally, exposure to AgNPs must be prevented or minimized during pregnancy or prenatal periods.
本研究旨在评估银纳米粒子(AgNPs)的遗传毒性,这种遗传毒性归因于其在怀孕大鼠体内的胎盘转移和组织分布。在妊娠第 19 天,怀孕大鼠经静脉(i.v.)注射大小为 4.0 至 17.0nm 的 AgNPs,剂量为 2mg/kg b.w.。除对照组外,每组 5 只大鼠,分别在注射后 10 分钟、1 小时、6 小时、12 小时和 24 小时处死。通过电感耦合等离子体发射光谱法对纳米粒子(NPs)在母体和胎儿组织中的积累进行定量,结果显示,注射后 24 小时,母体血液中的纳米粒子积累水平最高(0.523μg/ml)。AgNPs 诱导脾脏组织中的积累高于胎盘和胎儿组织匀浆。数据显示,与未处理的个体相比,所有给予 AgNPs 的动物收集样本中的 8-羟基脱氧鸟苷(8-hydroxydeoxyguanosine)水平均显著升高。羊水样本中的 8-OHdG 水平最高,其次是母体脾脏、肾脏和肝脏。透射电子显微镜检查显示,AgNPs 通过胎盘壁的转移导致核凹陷、染色质凝聚、固缩核和局灶性坏死区,而 AgNPs 主要积累在脾脏的巨噬细胞中。因此,数据表明,在对新型纳米粒子和纳米材料的安全性进行全面评估时,必须对 AgNPs 的遗传毒性进行研究。此外,在怀孕期间或产前必须防止或尽量减少 AgNPs 的暴露。