Sex difference in metabolism of simvastatin by rat hepatic microsomes

Eur J Drug Metab Pharmacokinet. 1992 Jul-Sep;17(3):175-81. doi: 10.1007/BF03190142.

Abstract

Metabolism of simvastatin (SV), a new cholesterol-lowering agent, by hepatic microsomes from male and female rats was investigated. After incubation of [14C]-SV with hepatic microsomes, radioactive metabolites were detected by HPLC. The main metabolite was 3' alpha-hydroxy-SV in male rats and the hydroxy open acid form of SV (SVA) in females. The 3"-hydroxy-SV and 3',3"-dihydroxy-SV which were observed in male rats were hardly detected in females. Specific activity for the metabolism of SV in male rats (3.97 nmol/mg protein/min) was about 9-times higher than that in females. Metabolic activity of hepatic microsomes in male rats was essentially unchanged with increase in age, whereas that in females decreased age-dependently and was very low or negligible after 7 weeks of age. Formation of 3"-hydroxy-SV and 3',3"-dihydroxy-SV in male rats was markedly increased with age, and that in females was negligible at all ages examined.

MeSH terms

  • Aging / metabolism
  • Animals
  • Anticholesteremic Agents / metabolism
  • Carbon Radioisotopes
  • Cytochrome P-450 Enzyme System
  • Female
  • Lovastatin / analogs & derivatives*
  • Lovastatin / metabolism
  • Male
  • Microsomes, Liver / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Sex Characteristics
  • Simvastatin

Substances

  • Anticholesteremic Agents
  • Carbon Radioisotopes
  • Cytochrome P-450 Enzyme System
  • Lovastatin
  • Simvastatin