Shanghai yufang yixue (Jun 2022)

Evaluation of mutagenicity of zinc oxide nanoparticles by Pig-a mutation assay in vivo

  • CHENG Xueqing,
  • YANG Jun,
  • LIU Xi,
  • SHAO Naimin,
  • HONG Xinyu

DOI
https://doi.org/10.19428/j.cnki.sjpm.2022.21549
Journal volume & issue
Vol. 34, no. 6
pp. 563 – 567

Abstract

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ObjectiveThe genotoxicity of zinc oxide nanoparticles (ZnO NPs) in rats was determined by Pig⁃a mutation assay in vivo.MethodsCombined with 28-day oral toxicity test, male SD rats were given ZnO NPs by oral administration for 28 days, at doses of 0, 14, 70 and 350 mg‧kg-1 (maximum concentration of nanoscale dispersion state). Rats in control groups received 350 mg‧kg-1 of normal size ZnO, 40 mg‧kg-1 N-ethyl-N⁃nitrosourea(ENU)or 0 mg·kg-1 ZnO NPs(solvent control group) Changes of body weight were recorded. At 0, 15, 28 d and 28 d of recovery observation period, 200 μL of tail venous blood was collected from each group, which was labeled by APC mouse anti-rat erythroid cells and FITC mouse anti-rat CD59. The information of 1×106 red blood cells(RBC) from each sample were collected by flow cytometry, and the mutation rate of RBCCD59- was calculated.ResultsCompared with the solvent control group, after 15 days of intragastric administration, the mutation rate of RBC CD59- in peripheral blood of in 350 mg‧kg-1 ZnO NPs group and 40 mg‧kg-1 ENU group was significantly increased while that of in 70 mg‧kg-1 ZnO NPs group was also significantly increased after 28 days of intragastric administration.with time-response and dose-response relationship. All groups except 40 mg‧kg-1 ENU group showed no significant difference in the mutation rate of RBCCD59- in peripheral blood in comparison with the solvent control group after 28-days recovery observation.Conclusion70 and 350 mg‧kg-1 ZnO NPs can increase the mutation rate of Pig⁃a gene in peripheral blood of SD rats.

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