Literature DB >> 115582

Renal tubular transport of methotrexate in the rhesus monkey and dog.

K C Huang, B A Wenczak, Y K Liu.   

Abstract

The mechanism and localization of renal transport of methotrexate (MTX) were studied in the rhesus monkey and the dog. It was found that in both animals MTX was bound with plasma protein in a range of 50 to 68% varying with the MTX plasma concentration. Paper chromatographic analysis showed that a negligible amount of MTX was metabolized. The excretion of MTX in rhesus monkey was mainly by tubular secretion which was blocked by probenecid, but in the dog a bidirectional transport mechanism for MTX was indicated. Tubular secretion was localized in the proximal tubules, and a tubular reabsorptive process was in the distal section. Simultaneous administration of folic acid blocked the tubular reabsorption of MTX, resulting in an increase of renal excretion. Maximum tubular excretory capacity determination showed that a maximum tubular excretory capacity value of approximately 5 mumol/100 ml of glomerular filtrate was observed in the rhesus monkey at a plasma concentration of 0.07 mM and a value of 2 mumol/100 ml of glomerular filtrate for the dog. Studies with renal cortical slice technique also indicated that the monkey kidney can accumulate greater amounts of MTX than can the dog kidney.

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Year:  1979        PMID: 115582

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  9 in total

1.  Urinary pH and urine flow independent renal clearance of methotrexate in dogs.

Authors:  C Y Lui; M G Lee; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1985-04

Review 2.  Clinical pharmacokinetics of drugs used in the treatment of breast cancer.

Authors:  V J Wiebe; C C Benz; M W DeGregorio
Journal:  Clin Pharmacokinet       Date:  1988-09       Impact factor: 6.447

3.  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

4.  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

5.  Concentration and pH dependent steady-state volume of distribution of methotrexate estimated by a simple physiologically based method.

Authors:  C Y Lui; M G Lee; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1984-12

6.  Influence of the antibiotics piperacillin, doxycycline, and tobramycin on the pharmacokinetics of methotrexate in rabbits.

Authors:  H Iven; H Brasch
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

7.  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

8.  Moment analysis of drug disposition in kidney. VI: Assessment of in vivo transmembrane transport of p-aminohippurate in tubular epithelium.

Authors:  Y L He; Y Tanigawara; A Kamiya; R Hori
Journal:  J Pharmacokinet Biopharm       Date:  1991-12

9.  Biochemical and pharmacological consequences of the interaction between methotrexate and ketoprofen in the rabbit.

Authors:  A Perrin; G Milano; A Thyss; P Cambon; M Schneider
Journal:  Br J Cancer       Date:  1990-11       Impact factor: 7.640

  9 in total

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