Red blood cell Pig-a assay and PIGRET assay in rats with azathioprine

Mutat Res Genet Toxicol Environ Mutagen. 2016 Nov 15:811:60-64. doi: 10.1016/j.mrgentox.2016.01.009. Epub 2016 Mar 8.

Abstract

A new in vivo gene mutation assay has been developed based on the phosphatidylinositol glycan anchor biosynthesis, Class A gene (Pig-a in rodents) as an endogenous reporter. Using this Pig-a assay, the in vivo mutagenicity of a single dose of azathioprine (Aza) was investigated in red blood cells (RBC Pig-a assay) and reticulocytes (PIGRET) of rats. Eight-week old male rats were orally dosed once with Aza at 50, 100 and 200mg/kg or ethylnitrosourea (ENU) at 10 and 40mg/kg as a positive control. Because 4 out of 6 animals at 200mg/kg of Aza died 3days after the dosing, this dose group was excluded for analyses. The frequencies of Pig-a mutants in RBCs and reticulocytes (RET) were evaluated once a week for 4 weeks after the treatment. With a single exposure to ENU, the frequencies of Pig-a mutants in both RBCs and RETs increased in a time- and dose-dependent manner. In contrast, with Aza small effects that were not statistically significant were observed in rats at 21 and 14days in the RBC Pig-a and PIGRET assays respectively. Based on the present results, the mutagenic potential of Aza is negligible after single oral administration in rats.

Keywords: Azathioprine; Gene mutation; Pig-a gene; Red blood cells; Reticulocytes.

MeSH terms

  • Animals
  • Azathioprine / toxicity*
  • Erythrocytes / drug effects*
  • Male
  • Membrane Proteins / genetics*
  • Mutagenicity Tests / methods*
  • Mutagens / toxicity*
  • Rats
  • Rats, Sprague-Dawley
  • Reticulocytes / drug effects*

Substances

  • Membrane Proteins
  • Mutagens
  • phosphatidylinositol glycan-class A protein
  • Azathioprine