Prolonged rest period enables the detection of micronucleated hepatocytes in the liver of young adult rats after a single dose of diethylnitrosamine or mitomycin C

Mutat Res Genet Toxicol Environ Mutagen. 2015 Sep:791:38-41. doi: 10.1016/j.mrgentox.2015.07.010. Epub 2015 Jul 28.

Abstract

A repeated-dose micronucleus assay utilizing young adult rat hepatocytes was recently developed to evaluate the genotoxicity. In this assay, accumulation of micronucleated hepatocytes (MNHEPs) induced by repeated dosing of genotoxic chemicals is considered to be a key factor in the detection of micronuclei induction. Then, we hypothesized that the period following chemical exposure enable the detection of MNHEP induction in young adult rats, namely that MNHEPs can be generated from chromosomally damaged cells and accumulate following initiation of chemical exposure until sampling. We therefore measured MNHEP induction at 2 or 4 weeks after a single oral administration of 12.5, 50, or 100mg/kg of diethylnitrosamine (DEN) or an intraperitoneal administration of 0.5, 1.0, or 2.0mg/kg of mitomycin C (MMC) to young adult rats. Results showed a statistically significant, dose-dependent increase in the numbers of MNHEPs in DEN- or MMC-treated rats, indicating that prolonged rest period following a single dose of a genotoxic chemical enables the detection of MNHEP induction in the liver of young adult rats. From these results, a single oral administration of 50mg/kg of DEN with a 2- or 4- week rest period can be used as a positive control in repeated-dose liver micronucleus assays. This procedure is superior in terms of labor saving and animal welfare to repeated dosing of DEN.

Keywords: Diethylnitrosamine; Liver micronucleus assay; Mitomycin C; Positive control for a repeated-dose liver micronucleus assay; Single-dose administration.

MeSH terms

  • Administration, Oral
  • Animals
  • DNA Damage*
  • Diethylnitrosamine / administration & dosage
  • Diethylnitrosamine / toxicity*
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Hepatocytes / drug effects*
  • Injections, Intraperitoneal
  • Micronucleus Tests / methods
  • Mitomycin / administration & dosage
  • Mitomycin / toxicity*
  • Mutagens / administration & dosage
  • Mutagens / toxicity*
  • Rats

Substances

  • Mutagens
  • Diethylnitrosamine
  • Mitomycin