Species variability in the stereoselective N-oxidation of pargyline

Chirality. 1994;6(2):91-7. doi: 10.1002/chir.530060209.

Abstract

The monoamine oxidase inhibitor pargyline (N-benzyl-N-methyl-2-propynylamine) is known to undergo extensive in vitro microsomal N-oxidation, thought to be mediated predominantly by the flavin-containing monooxygenase (FMO) enzyme system. Formation of the pargyline N-oxide (PNO) metabolite creates a chiral nitrogen centre and thus asymmetric oxidation is possible. This study describes a reverse-phase high-performance liquid chromatographic (HPLC) method for the quantitation of PNO and a chiral-phase HPLC method for the determination of the enantiomeric ratio of PNO. In vitro microsomal N-oxidation of pargyline was found to be highly stereoselective in a number of species, with the (+)-enantiomer being formed preferentially. This metabolic transformation was stereospecific when purified porcine hepatic FMO was used as the enzyme source.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid
  • Guinea Pigs
  • In Vitro Techniques
  • Magnetic Resonance Spectroscopy
  • Male
  • Mice
  • Mice, Inbred DBA
  • Microsomes, Liver / enzymology
  • Optical Rotation
  • Oxidation-Reduction
  • Oxygenases / metabolism
  • Pargyline / analogs & derivatives
  • Pargyline / metabolism
  • Pargyline / pharmacokinetics*
  • Rabbits
  • Rats
  • Rats, Wistar
  • Species Specificity
  • Spectrophotometry, Ultraviolet
  • Stereoisomerism
  • Swine

Substances

  • pargyline N-oxide
  • Pargyline
  • Oxygenases
  • dimethylaniline monooxygenase (N-oxide forming)