Polymorphic hydroxylation of Debrisoquine in man

Lancet. 1977 Sep 17;2(8038):584-6. doi: 10.1016/s0140-6736(77)91430-1.

Abstract

Debrisoquine and its primary metabolite, 4-hydroxydebrisoquine, were measured in the urine of 94 volunteers after a single oral dose of 10 mg debrisoquine. The ratio between excreted debrisoquine and its metabolite was bimorphically distributed in the study population. Family studies supported the view that alicyclic 4-hydroxylation of debrisoquine is controlled by a single autosomal gene and that a defect in this metabolic step is caused by a recessive allele.

MeSH terms

  • Administration, Oral
  • Adolescent
  • Adult
  • Alleles
  • Biological Availability
  • Chemical Phenomena
  • Chemistry
  • Child
  • Debrisoquin / administration & dosage
  • Debrisoquin / analogs & derivatives
  • Debrisoquin / urine*
  • Female
  • Genes, Recessive
  • Genotype
  • Humans
  • Hydroxylation
  • Isoquinolines / urine*
  • Male
  • Metabolism, Inborn Errors / genetics
  • Middle Aged

Substances

  • Isoquinolines
  • Debrisoquin