In vivo-in vitro relationship of methotrexate 7-hydroxylation by aldehyde oxidase in four different strain rats

Drug Metab Pharmacokinet. 2006 Dec;21(6):485-91. doi: 10.2133/dmpk.21.485.

Abstract

The in vivo metabolism of methotrexate (MTX) to 7-hydroxymethotrexate (7-OH-MTX) was studied using four strains of rats. When MTX was administered to these rats, 7-OH-MTX was detected as the major in vivo metabolite, mainly in bile and feces, and also slightly in the urine. There were marked strain differences in the amounts of 7-OH-MTX excreted in bile, feces and urine. The highest recovery of 7-OH-MTX in bile, feces and urine was observed in Sea:SD rats (6.2%, 4.2% and 0.8% of dose, respectively), followed by Jcl:SD and Crj:SD rats. The lowest recovery (0.02%, 0.2% and 0.003%, respectively) was observed in WKA/Sea rats. The variations of excreted amount of 7-OH-MTX were closely correlated with the strain differences of cytosolic MTX 7-hydroxylase and benzaldehyde oxidase activities. Our results indicate that variation of formation of 7-OH-MTX from MTX in vivo in rats is due primarily to variation of aldehyde oxidase.

MeSH terms

  • Aldehyde Oxidase / metabolism*
  • Animals
  • Bile / metabolism
  • Cytosol / metabolism
  • Feces / chemistry
  • Folic Acid Antagonists / metabolism
  • Folic Acid Antagonists / pharmacokinetics
  • Folic Acid Antagonists / urine
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Methotrexate / analogs & derivatives*
  • Methotrexate / metabolism
  • Methotrexate / pharmacokinetics
  • Rats
  • Rats, Inbred Strains
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Species Specificity

Substances

  • Folic Acid Antagonists
  • Aldehyde Oxidase
  • 7-hydroxymethotrexate
  • Methotrexate