Literature DB >> 187352

Modifications of drug metabolism by disulfiram and diethyldithiocarbamate. I. Mixed-function oxygenase.

M Lang, M Marselos, R Törrönen.   

Abstract

Disulfiram and diethyldithiocarbamate were administered to rats for 4 days alone (300 mg/kg, daily, per os) or in combination with phenobarbital (80 mg/kg, daily, i.p.), in order to observe the effects of these compounds on the microsomal membrane components and on the mixed-function oxygenase system. Both disulfiram and diethyldithiocarbamate increased the liver to body weight ratio, and the total hepatic protein content. Disulfiram significantly increased also the microsomal protein and phospholipid contents. Diethyldithiocarbamate and disulfiram partially prevented the increase of microsomal protein and phospholipid contents caused by phenobarbital. Disulfiram and diethyldithiocarbamate decreased the amount of cytochrome P-450 and P-420, and the activity of p-nitroanisole O-demethylase. These changes were more pronounced after diethyldithiocarbamate than after disulfiram treatment. On the contrary, the activity of NADPH-cytochrome c reductase was enhanced only by disulfiram. The induction by phenobarbital of cytochrome P-450 and p-nitrosanisole O-demethylase was partially prevented on concomitant treatment with disulfiram and diethyldithiocarbamate. These compounds. however, had an additive effect with phenobarbital in enhancing the microsomal NADPH-cytochrome c reductase activity.

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Year:  1976        PMID: 187352     DOI: 10.1016/0009-2797(76)90152-6

Source DB:  PubMed          Journal:  Chem Biol Interact        ISSN: 0009-2797            Impact factor:   5.192


  4 in total

1.  Urinary excretion of ethylenethiourea and kidney morphology in rats after continuous oral exposure to nabam or ethylenethiourea.

Authors:  P Kurttio; K Savolainen; A Naukkarinen; V M Kosma; L Tuomisto; I Penttilä; J Jolkkonen
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

2.  Further studies on dimethylnitrosamine metabolism, activation and its ability to cause liver injury.

Authors:  M I Diaz Gomez; H M Godoy; J A Castro
Journal:  Arch Toxicol       Date:  1981-06       Impact factor: 5.153

3.  Changes in the inducibility of a hepatic aldehyde dehydrogenase by various effectors.

Authors:  V Vasiliou; M Marselos
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

4.  Parathion-provoked lethality in rats is reduced by diethyldithiocarbamate.

Authors:  J Homann; S Schneider; K J Matthes
Journal:  Arch Toxicol       Date:  1985-06       Impact factor: 5.153

  4 in total

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