Mechanisms related to reduction of radical in mouse lung using an L-band ESR spectrometer

Free Radic Biol Med. 1999 Apr;26(7-8):951-60. doi: 10.1016/s0891-5849(98)00278-0.

Abstract

Reduction of radicals in mouse lung was characterized in whole animals using an L-band ESR technique and nitroxide radicals as probes. An aqueous solution of nitroxide radical was immediately instilled intratracheally to mouse after euthanasia. Nitroxide radicals without charged groups were reduced significantly in the lung, while radicals with charged groups were only slightly reduced. Permeation rates across lung plasma membrane were not rate limiting of the stage of reduction of the noncharged nitroxides. Michaelis parameters, apparent Km and apparent Vmax, were obtained from the Lineweaver-Burk plots of the reduction. Among noncharged nitroxides with constant apparent Vmax, radicals with a larger n-octanol/water partition coefficient showed a lower apparent Km, thereby suggesting that the concentration of these nitroxides in the membrane contributes to apparent Km. The reduction rate of noncharged nitroxide, hydroxy-TEMPO, was influenced by noncharged SH reagents instilled together with the nitroxide; dithiothreitol stimulated the reduction, while the oxidized reagent inhibited it. The Lineweaver-Burk plots of the nitroxide reduction in the presence of various concentrations of dithiothreitol suggest the possibility that the reduction system for hydroxy-TEMPO is based on a kind of ping pong bi-reactant mechanism, and that the reduction system utilizes SH as an electron donor. Endogenous glutathione contributed partially to the reduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Membrane Permeability
  • Dithionitrobenzoic Acid
  • Dithiothreitol / pharmacology
  • Electron Spin Resonance Spectroscopy / instrumentation
  • Electron Spin Resonance Spectroscopy / methods
  • Female
  • Kinetics
  • Lung / drug effects
  • Lung / metabolism*
  • Mice
  • Mice, Inbred Strains
  • Nitrogen Oxides / pharmacokinetics*
  • Oxidation-Reduction
  • Pulmonary Alveoli / metabolism*
  • Spin Labels
  • Sulfhydryl Compounds / analysis

Substances

  • Nitrogen Oxides
  • Spin Labels
  • Sulfhydryl Compounds
  • Dithionitrobenzoic Acid
  • Dithiothreitol