Literature DB >> 9248779

The effect of velnacrine on the mixed function oxidase system.

M J Eccles1, T C Danbury, J M Ford, C J Roberts.   

Abstract

Velnacrine is a centrally acting anticholinesterase which has been considered for use in the treatment of Alzheimer's disease. If proven to be of value, it will be used concurrently with other medications. Its potential to cause interaction is, therefore, important to study. The aim of this work was to investigate velnacrine as an inhibitor of hepatic oxidative enzymes. The effects of velnacrine on antipyrine metabolism in isolated rat hepatic microsomes were compared to those of cimetidine. Aliquots of 200, 250 and 300 micrograms/ml antipyrine were incubated alone, with 20 micrograms/ml cimetidine and with each of 20, 50 and 100 micrograms/ml velnacrine. The concentrations of antipyrine and of its metabolites, 3-hydroxymethylantipyrine, 4-hydroxyantipyrine and norantipyrine were assayed by reverse phase high performance liquid chromatography. Cimetidine inhibited production of all three metabolites. Velnacrine did not affect 3-hydroxymethylantipyrine production. Mean inhibition of 4-hydroxyantipyrine production of 15%, 30% and 25% (P < 0.01), and of 14%, 25% and 12% of norantipyrine production (P < 0.01) occurred. These results indicate that velnacrine may inhibit the enzymes responsible for the metabolism of antipyrine to norantipyrine and 4-hydroxyantipyrine. The clearance rate of drugs that are metabolised through the hepatic oxidase system may, therefore, be reduced in the presence of concurrent treatment with velnacrine.

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Year:  1997        PMID: 9248779     DOI: 10.1007/BF03189794

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.569


  21 in total

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Journal:  Xenobiotica       Date:  1990-11       Impact factor: 1.908

2.  Evaluation of HP 029 (velnacrine maleate) in Alzheimer's disease.

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Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

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Authors:  E Rekka; G J Sterk; H Timmerman; A Bast
Journal:  Chem Biol Interact       Date:  1988       Impact factor: 5.192

4.  Identification of the human hepatic cytochromes P450 involved in the in vitro oxidation of antipyrine.

Authors:  J E Sharer; S A Wrighton
Journal:  Drug Metab Dispos       Date:  1996-04       Impact factor: 3.922

5.  Interindividual variations in drug disposition. Clinical implications and methods of investigation.

Authors:  D D Breimer
Journal:  Clin Pharmacokinet       Date:  1983 Sep-Oct       Impact factor: 6.447

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Authors:  A Somogyi; R Gugler
Journal:  Clin Pharmacokinet       Date:  1982 Jan-Feb       Impact factor: 6.447

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Authors:  O Pelkonen; J Puurunen
Journal:  Biochem Pharmacol       Date:  1980-11-15       Impact factor: 5.858

8.  Antipyrine metabolism in the rat by three hepatic monooxygenases.

Authors:  T Inaba; M Lucassen; W Kalow
Journal:  Life Sci       Date:  1980-06-09       Impact factor: 5.037

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Authors:  E M Sorkin; D L Darvey
Journal:  Drug Intell Clin Pharm       Date:  1983-02

10.  The nucleus basalis of Meynert in neurological disease: a quantitative morphological study.

Authors:  J D Rogers; D Brogan; S S Mirra
Journal:  Ann Neurol       Date:  1985-02       Impact factor: 10.422

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  1 in total

1.  Effect of tacrine hydrochloride on hepatic drug metabolism.

Authors:  T C Danbury; M Eccles; J Ford; C J Roberts
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1999 Jan-Mar       Impact factor: 2.569

  1 in total

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