Morphine metabolism revisited. II. Isolation and chemical characterization of a glutathionylmorphine adduct from rat liver microsomal preparations

Chem Biol Interact. 1984 Sep 1;51(1):13-24. doi: 10.1016/0009-2797(84)90016-4.

Abstract

Incubation of tritium-labeled morphine and cold glutathione (GSH) or cold morphine and tritiated GSH with liver microsomal preparations obtained from phenobarbital-treated rats led to the identification by high performance liquid chromatography (HPLC) of a glutathionylmorphine adduct. Liquid secondary ion mass spectral analysis established the molecular weight of the metabolite to be 590 which corresponds to the mass of a mono-GSH-morphine adduct. High resolution (360 and 500 MHz) 1H-NMR experiments have led to the tentative assignment of the structure of this metabolite as 10-alpha-S-glutathionylmorphine. Based on both in vivo and in vitro data, the formation of this product appears to be mediated by cytochrome P-450 and to involve a reactive intermediate that may be responsible for the observed covalent binding of radiolabeled morphine to proteins and, at least in part, for the morphine-induced depletion of GSH in the rat.

Publication types

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

MeSH terms

  • Animals
  • Glutathione / analogs & derivatives*
  • Glutathione / isolation & purification
  • Glutathione / metabolism
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism*
  • Morphine / metabolism*
  • Morphine Derivatives / isolation & purification*
  • Phenobarbital / pharmacology
  • Rats
  • Tritium

Substances

  • Morphine Derivatives
  • Tritium
  • Morphine
  • 10-alpha-S-glutathionylmorphine
  • Glutathione
  • Phenobarbital