Reversible inhibition of aromatic hydroxylation of methamphetamine in rat liver microsomal preparations pretreated with methamphetamine

Biochem Pharmacol. 1988 Apr 15;37(8):1433-7. doi: 10.1016/0006-2952(88)90003-2.

Abstract

The effects of a single and repeated administration of methamphetamine (MP) in vivo in rats on its own metabolism in vitro were investigated. In both cases, the p-hydroxylation of MP to p-hydroxymethamphetamine by a microsomal fraction from rat liver was inhibited for a period of 16 hr after the last injection of MP. This inhibition was diminished by dialysis of the microsomal preparations. In contrast, the reduced level of cytochrome P-450 in hepatic microsomes from rats pretreated with the SKF 525-A did not revert to the control value after dialysis. When microsomes were preincubated with N-hydroxymethamphetamine, which is the metabolite of MP and a potent substrate for the formation of a metabolic intermediate (MI) complex with cytochrome P-450, the content of the MI was increased and the MP-hydroxylation activity decreased in direct proportion to the length of the preincubation. These results suggest that the inhibition of MP-hydroxylation may be due to reduction of the level of cytochrome P-450 that accompanies the formation of the MI complex. Furthermore, it appears that the complex can be dissociated by dialysis.

MeSH terms

  • Animals
  • Cytochrome P-450 Enzyme System / metabolism
  • Dialysis
  • Hydroxylation
  • In Vitro Techniques
  • Male
  • Methamphetamine / analogs & derivatives
  • Methamphetamine / metabolism
  • Methamphetamine / pharmacology*
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism*
  • Rats
  • Rats, Inbred Strains

Substances

  • Methamphetamine
  • N-hydroxymethamphetamine
  • Cytochrome P-450 Enzyme System