Abstract

In the food and fertilizer industries, zinc oxide nanoparticles (ZnO-NPs) are frequently utilized. Our study conducted to assess the genotoxicity, biochemical alterations and histopathological parameters of ZnO NPs with a particle size of 30 ± 5 nm were orally administered to rats once daily at doses of 100, 200, 300, 400, and 600 mg/kg for ten week. The experiment involved the use of 30 Sprague–Dawley male rats exposed to various concentrations of ZnO-NPs. After the adaptation period, six groups were created out of the thirty rats (Five rats per group). Rats in Group 1 (G1), known as the control group, were fed a standard synthetic meal and had unlimited access to drinking water ad libitum, while those in the other five groups received oral gavage treatments with various doses of zinc oxide nanoparticles over a 10-week period. The results indicated that ZnO-NPs induces a lowering in body weight beginning in the sixth week while increasing serum AST, ALT, creatinine, and uric acid activity. However, the addition of different concentrations of ZnO NPs compared to the control caused insignificantly decreased on the plasma glucose level in all treated animals. Numerous chromosomal aberrations, including fragments, chromosome rings, chromatid breaks, end-to-end association, and centric fusion, were observed through cytogenetic investigation. When compared to the control group, hepatic vacuolation, large sinusoidal dilatation, degenerative alterations, and cellular congestion were observed in the liver of the male rats treated with 400 and 600 mg/kg of ZnO-NPs. According to the findings of in vivo genotoxicity experiments, rats' bone marrow cells, liver, and kidney can exhibit genotoxicity and cytotoxicity after exposed to ZnO NPs with particle sizes of 30 nm for ten weeks. The findings of this study could raise more concerns regarding the potential damage to human health associated with the widespread use of ZnO NPs.

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