Toxicity of ZnO nanoparticles in healthy adult mice

Environ Toxicol Pharmacol. 2013 Jan;35(1):67-71. doi: 10.1016/j.etap.2012.11.003. Epub 2012 Nov 23.

Abstract

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.

MeSH terms

  • Administration, Oral
  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Cholesterol / blood
  • Female
  • Gonadal Steroid Hormones / blood
  • Kidney / drug effects
  • Kidney / pathology
  • L-Lactate Dehydrogenase / blood
  • Liver / drug effects
  • Liver / pathology
  • Lung / drug effects
  • Lung / pathology
  • Mice
  • Nanoparticles / toxicity*
  • Rats
  • Rats, Wistar
  • Triglycerides / blood
  • Uterus / drug effects
  • Uterus / pathology
  • Zinc Oxide / toxicity*

Substances

  • Gonadal Steroid Hormones
  • Triglycerides
  • Cholesterol
  • L-Lactate Dehydrogenase
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Zinc Oxide