Formation of 7-(4-oxobutyl)guanine in hepatic DNA of rats treated with N-nitrosopyrrolidine

Carcinogenesis. 1992 Oct;13(10):1909-11. doi: 10.1093/carcin/13.10.1909.

Abstract

We have reported previously the formation of two structurally distinct exocyclic guanine adducts (adducts 1 and 6) in liver DNA of F344 rats treated with N-nitrosopyrrolidine (NPYR). In this study, we detected and characterized a previously unidentified guanine adduct in liver DNA of NPYR-treated rats. The structure of this adduct was established as 7-(4-oxobutyl)guanine (adduct 2) by comparison with the synthetic standard and confirmed by NaBH4 reduction to 7-(4-hydroxybutyl)guanine. The level of adduct 2 in liver DNA of F344 rats treated with 450 mg/kg of NPYR by i.p. administration was 643 +/- 9 mumol/mol guanine, approximately one-third of the level of adduct 1. This study is the first to demonstrate the in vivo formation of a formylalkyl-substituted guanine adduct by a nitrosamine.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid
  • DNA / metabolism*
  • Deoxyribonucleosides / analysis
  • Deoxyribonucleosides / metabolism
  • Guanine / analogs & derivatives*
  • Guanine / analysis
  • Guanine / biosynthesis
  • Hot Temperature
  • Hydrolysis
  • Liver / metabolism*
  • Male
  • N-Nitrosopyrrolidine / metabolism
  • N-Nitrosopyrrolidine / pharmacology*
  • Rats
  • Rats, Inbred F344
  • Tritium

Substances

  • Deoxyribonucleosides
  • Tritium
  • 7-(4-oxobutyl)guanine
  • Guanine
  • DNA
  • N-Nitrosopyrrolidine