The effect of allyl compounds on hepatic microsomal mixed function oxidation and porphyrogenesis

Chem Biol Interact. 1976 Aug;14(3-4):241-9. doi: 10.1016/0009-2797(76)90104-6.

Abstract

The activities of 5-aminolaevulinate (5-ALA) synthetase and of various microsomat drug-metabolising enzymes have been determined in the livers of rats pretreated with different drugs and chemicals containing the allyl group. Safrole, isosafrole and secobarbital gave rise to slight increases in 5-ALA synthetase, whereas alclophenac and triallyl cyanurate almost doubled the enzyme activity and the known porphyrogenic agents, allylisopropylacetamide (AIA) and allobarbital caused increases of 1.5- and 2.5-fold, respectively. Allobarbital induced the microsomal drug-metabolising enzymes while secobarbital had only a weak effect and alclophenac and triallyl cyanurate had no effect at all. From these results it is suggested that induction of the synthesis of cytochrome P-450 is not rate dependent on the synthesis haem and induction of porphyrin biosynthesis.

MeSH terms

  • 5-Aminolevulinate Synthetase / metabolism*
  • Allyl Compounds / pharmacology*
  • Allylisopropylacetamide / pharmacology
  • Animals
  • Barbiturates / pharmacology
  • Ethylmorphine-N-Demethylase / metabolism
  • Liver / drug effects
  • Liver / enzymology*
  • Male
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism*
  • Mixed Function Oxygenases / metabolism*
  • Oxidoreductases / metabolism*
  • Porphyrins / biosynthesis*
  • Rats
  • Safrole / pharmacology
  • Secobarbital / pharmacology
  • Structure-Activity Relationship

Substances

  • Allyl Compounds
  • Barbiturates
  • Porphyrins
  • Secobarbital
  • Allylisopropylacetamide
  • Mixed Function Oxygenases
  • Oxidoreductases
  • Ethylmorphine-N-Demethylase
  • 5-Aminolevulinate Synthetase
  • Safrole