Literature DB >> 3382415

Inhibition of rat liver glutathione S-transferase isoenzymes by acrolein.

T R Scott1, R E Kirsch.   

Abstract

The in vitro effect of the toxin and teratogen, acrolein, on the fetal rat liver glutathione S-transferase isoenzyme, YcYfetus, was investigated and compared with acrolein's effect on some of the adult rat liver glutathione S-transferase isoenzymes. Acrolein was found to inhibit all the isoenzymes investigated and double-reciprocal plots suggest that inhibition is either noncompetitive or mixed-type noncompetitive. It is therefore attractive to suggest that should a similar situation arise in vivo, it may provide one mechanism for the teratogenicity of acrolein.

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Year:  1988        PMID: 3382415

Source DB:  PubMed          Journal:  Biochem Int        ISSN: 0158-5231


  2 in total

Review 1.  Clinical pharmacokinetics of cyclophosphamide.

Authors:  Milly E de Jonge; Alwin D R Huitema; Sjoerd Rodenhuis; Jos H Beijnen
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 5.577

2.  High exposures to bioactivated cyclophosphamide are related to the occurrence of veno-occlusive disease of the liver following high-dose chemotherapy.

Authors:  M E de Jonge; A D R Huitema; J H Beijnen; S Rodenhuis
Journal:  Br J Cancer       Date:  2006-05-08       Impact factor: 7.640

  2 in total

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