Literature DB >> 6847701

Formation and disposition of 7-hydroxymethotrexate in rabbits.

K Sasaki, R Hosoya, Y M Wang, G L Raulston.   

Abstract

The metabolism of methotrexate in rabbits was investigated following 6 hr of infusion with [3',5',7-(3)H]methotrexate (50 mg/kg). Methotrexate and its metabolites were analyzed by an enzyme kinetic method, reverse phase high-performance liquid chromatography, and scintillation counting of radioactivity. 7-Hydroxymethotrexate was found to be a major metabolite in plasma, urine, bile and various tissues of rabbits. Cumulative production of 7-hydroxymethotrexate during the first 6 hr was 31.8% of the total dose. The peak 7-hydroxymethotrexate concentration in plasma was reached at the end of the infusion, and this concentration was higher than the methotrexate concentration. The plasma clearance of 7-hydroxymethotrexate was biphasic in nature and slower than that of methotrexate. The highest methotrexate concentration was found in kidney after 6 hr. This concentration was found to be 7.2 times greater than that in plasma. A higher ratio of 7-hydroxymethotrexate/methotrexate was found in liver, small intestine, kidney and testis when compared to plasma. Lung and kidney showed significant conversion of methotrexate to 7-hydroxymethotrexate in vitro, as did the liver.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6847701     DOI: 10.1016/0006-2952(83)90530-0

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  11 in total

1.  Determination of free extracellular levels of methotrexate by microdialysis in muscle and solid tumor of the rabbit.

Authors:  S Dukic; M L Kaltenbach; B Gourdier; H Marty; R Vistelle
Journal:  Pharm Res       Date:  1998-01       Impact factor: 4.200

Review 2.  Clinical pharmacokinetics of methotrexate in children.

Authors:  Y M Wang; T Fujimoto
Journal:  Clin Pharmacokinet       Date:  1984 Jul-Aug       Impact factor: 6.447

3.  Substrate specificity of guinea pig liver aldehyde oxidase and bovine milk xanthine oxidase for methyl- and nitrobenzaldehydes.

Authors:  Aristidis S Veskoukis; Demetrios Kouretas; Georgios I Panoutsopoulos
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2006 Jan-Mar       Impact factor: 2.441

4.  Cephalosporins increase the renal clearance of methotrexate and 7-hydroxymethotrexate in rabbits.

Authors:  H Iven; H Brasch
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

5.  Evaluation of methotrexate tissue exposure by in situ microdialysis in a rat model.

Authors:  O Ekstrøm; A Andersen; D J Warren; K E Giercksky; L Slørdal
Journal:  Cancer Chemother Pharmacol       Date:  1994       Impact factor: 3.333

6.  Pharmacokinetics of methotrexate and 7-hydroxy-methotrexate in rabbits.

Authors:  H Iven; H Brasch; J Engster
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

7.  The effects of antibiotics and uricosuric drugs on the renal elimination of methotrexate and 7-hydroxymethotrexate in rabbits.

Authors:  H Iven; H Brasch
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

8.  Pharmacokinetics and pharmacodynamics of low-dose methotrexate in the treatment of psoriasis.

Authors:  Jaroslav Chládek; Jiøí Grim; Jiøina Martínková; Marie Simková; Jaroslava Vanìèková; Vìra Koudelková; Marie Noièková
Journal:  Br J Clin Pharmacol       Date:  2002-08       Impact factor: 4.335

9.  Pharmacokinetics of methotrexate (MTX) and 7-hydroxymethotrexate (7-OH-MTX) in rats and evidence for the metabolism of MTX to 7-OH-MTX.

Authors:  L Fahrig; H Brasch; H Iven
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

10.  Inhibition of 7-hydroxymethotrexate formation by amsacrine.

Authors:  R M Bremnes; E Smeland; N P Willassen; E Wist; J Aarbakke
Journal:  Cancer Chemother Pharmacol       Date:  1991       Impact factor: 3.333

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.