Islamic Azad University, Science and Research Branch, Department of Science, Urmia, Iran.
Environ Toxicol Pharmacol. 2013 Jan;35(1):67-71. doi: 10.1016/j.etap.2012.11.003. Epub 2012 Nov 23.
In this study, we extended previous work to evaluate the oral toxicity of ZnO nanoparticles and their possible effects on different serum-elements and sexual hormones in the mouse. The histopathological changes have also been examined. Significant recorded increases in alanine aminotransferase and aspartate aminotransferase activity in all mice exposed to ZnO nanoparticles suggest that these nanoparticles can cause hepatic injury. Hepatocyte necrosis and other pathological observations also confirmed liver damage. Moreover, Glomeruli segmentation, hydropic degeneration in epithelial cells, necrosis of epithelial cells in tubules and swelling in epithelial cells of proximal tubules were found in all kidney tissues, which demonstrated that ZnO nanoparticles have severe toxicological effects on kidney. Serous inflammation, severe hyperemia in alveoli, and edema were observed as pathological findings in the lung which suggest that the lung is the third target tissue of the ZnO nanoparticles.
在这项研究中,我们扩展了之前的工作,评估了氧化锌纳米粒子的口服毒性及其对小鼠不同血清元素和性激素的可能影响。还检查了组织病理学变化。暴露于氧化锌纳米粒子的所有小鼠的丙氨酸氨基转移酶和天冬氨酸氨基转移酶活性显著升高,表明这些纳米粒子可能导致肝损伤。肝细胞坏死和其他病理观察也证实了肝损伤。此外,所有肾脏组织中均发现肾小球分割、上皮细胞水肿变性、小管上皮细胞坏死和近端小管上皮细胞肿胀,表明氧化锌纳米粒子对肾脏有严重的毒理学影响。肺部的病理发现为浆液性炎症、肺泡严重充血和水肿,表明肺部是氧化锌纳米粒子的第三个靶组织。