Article ID Journal Published Year Pages File Type
2583322 Environmental Toxicology and Pharmacology 2013 5 Pages PDF
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.

► ZnO nanoparticles can induce their toxic effects on different organs in five days. ► ZnO nanoparticles can cause lung, liver and kidney damages. ► ZnO nanoparticles can decrease serum HDL and LDL level. ► The trace damage of reproductive organs was detected in further histopathological examinations.

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Life Sciences Environmental Science Health, Toxicology and Mutagenesis
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