Direct evidence for in vivo hydroxyl radical generation in blood of mice after acute chromium(VI) intake: electron spin resonance spin-trapping investigation

Biol Trace Elem Res. 2000 Jul;76(1):75-84. doi: 10.1385/BTER:76:1:75.

Abstract

Although it is assumed from in vitro experiments that the hydroxyl radical (*OH) may be responsible for chromium(VI) toxicity/carcinogenicity, no electron spin resonance (ESR) evidence for the generation of *OH in vivo has been reported. In this study, we have employed an ESR spin-trapping technique with 5,5-dimethylpyrroline-N-oxide (DMPO), a selective *OH trap, to detect *OH in blood. The ESR spectrum of spin adduct observed in the blood of mice given 4.8 mmol Cr(VI)/kg body weight exhibited the 1:2:2:1 intensity pattern of a quartet with a hyperfine coupling constant A(N) = A(H) = 14.81 G and g-value = 2.0067. The concentration of the spin adduct detected in the blood was 7.37 microM. The adduct production was inhibited by the addition of specific *OH scavengers such as sodium benzoate and methional to the blood. The results indicate that the spin adduct is nitroxide produced by the reaction of *OH with DMPO. This is the first report of ESR evidence for the in vivo generation of *OH in mammals by Cr(VI).

MeSH terms

  • Aldehydes / chemistry
  • Animals
  • Chromium / pharmacokinetics*
  • Cyclic N-Oxides / chemistry
  • Electron Spin Resonance Spectroscopy
  • Hydroxyl Radical / blood*
  • Hydroxyl Radical / toxicity
  • Male
  • Mice
  • Sodium Benzoate / chemistry
  • Spectrophotometry, Atomic
  • Time Factors

Substances

  • Aldehydes
  • Cyclic N-Oxides
  • methional
  • Chromium
  • Hydroxyl Radical
  • 5,5-dimethyl-1-pyrroline-1-oxide
  • Sodium Benzoate