Literature DB >> 7003365

Substrates and inhibitors of hepatic amine oxidase inhibit dimethylnitrosamine-induced mutagenesis in Salmonella typhimurium.

I R Rowland, B G Lake, J C Phillips, S D Gangolli.   

Abstract

The mutagenic effect of dimethylnitrosamine in Salmonella typhimurium TA100, in the presence of a rat-liver homogenate derived from animals treated with Aroclor 1254, was inhibited by substrates and inhibitors of monoamine oxidase. Substrates of diamine oxidase did not inhibit dimethylnitrosamine mutagenesis and, furthermore, monoamine oxidase inhibitors had no effect on mutagenesis by benzo[a]pyrene or aflatoxin B1. The results suggest that monoamine oxidase participates in the activation of dimethylnitrosamine to a mutagen.

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Year:  1980        PMID: 7003365     DOI: 10.1016/0027-5107(80)90221-3

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  4 in total

1.  Quantitative analysis of flux along the gluconeogenic, glycolytic and pentose phosphate pathways under reducing conditions in hepatocytes isolated from fed rats.

Authors:  J M Crawford; J J Blum
Journal:  Biochem J       Date:  1983-06-15       Impact factor: 3.857

2.  The effect of mixed-function oxidase and amine oxidase inhibitors on the activation of dialkylnitrosamines and 1,2-dimethylhydrazine to bacterial mutagens in mice.

Authors:  P R Kerklaan; S Bouter; J A Zijlstra; G R Mohn
Journal:  J Cancer Res Clin Oncol       Date:  1986       Impact factor: 4.553

3.  Formation of N-alkylated protoporphyrin IX in the livers of mice after diethylnitrosamine treatment.

Authors:  I N White; A G Smith; P B Farmer
Journal:  Biochem J       Date:  1983-06-15       Impact factor: 3.857

4.  N-nitrosodialkylamines do not function as substrates for liver monoamine oxidase.

Authors:  D E Edmondson; T C Bruice
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

  4 in total

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