Inhibitors of imipramine metabolism by human liver microsomes

Br J Clin Pharmacol. 1992 Sep;34(3):256-61. doi: 10.1111/j.1365-2125.1992.tb04133.x.

Abstract

1. The aromatic 2-hydroxylation of imipramine was studied in microsomes from three human livers. The kinetics were best described by a biphasic enzyme model. The estimated values of Vmax and Km for the high affinity site ranged from 3.2 to 5.7 nmol mg-1 h-1 and from 25 to 31 microM, respectively. 2. Quinidine was a potent inhibitor of the high affinity site for the 2-hydroxylation of imipramine in microsomes from all three human livers, with apparent Ki-values ranging from 9 to 92 nM. This finding strongly suggests that the high affinity enzyme is CYP2D6, the source of the sparteine/debrisoquine oxidation polymorphism. 3. The selective serotonin reuptake inhibitors (SSRI), paroxetine, fluoxetine and norfluoxetine were potent inhibitors of the high affinity site having apparent Ki-values of 0.36, 0.92 and 0.33 microM, respectively. Three other SSRIs, citalopram, desmethylcitalopram and fluvoxamine, were less potent inhibitors of CYP2D6, with apparent Ki-values of 19, 1.3 and 3.9 microM, respectively. 4. Among 20 drugs screened, fluvoxamine was the only potent inhibitor of the N-demethylation of imipramine, with a Ki-value of 0.14 microM. 5. Neither mephenytoin, citalopram, diazepam, omeprazole or proguanil showed any inhibition of the N-demethylation of imipramine and the role of the S-mephenytoin hydroxylase for this oxidative pathway could not be confirmed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytochrome P-450 CYP2D6
  • Cytochrome P-450 Enzyme Inhibitors*
  • Fluvoxamine / pharmacology*
  • Humans
  • Hydroxylation
  • Imipramine / metabolism*
  • In Vitro Techniques
  • Kinetics
  • Microsomes, Liver / metabolism*
  • Mixed Function Oxygenases / antagonists & inhibitors*
  • Polymorphism, Genetic
  • Quinidine / pharmacology*
  • Serotonin Uptake Inhibitors / pharmacology*

Substances

  • Cytochrome P-450 Enzyme Inhibitors
  • Serotonin Uptake Inhibitors
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP2D6
  • Quinidine
  • Fluvoxamine
  • Imipramine