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Enzyme specific kinetics of 1,2-epoxybutene-3 in microsomes and cytosol from livers of mouse, rat, and man.

Abstract
Kinetics of the metabolism of 1,2-epoxybutene-3 (butadiene monoxide) were investigated in liver fractions of mouse, rat, and man. In these species similar enzyme characteristics were found. In microsomes, no NADPH-dependent metabolism of butadiene monoxide was detectable. Epoxide hydrolase activity was found only in microsomes. The Vmax [nmol butadiene monoxide/(mg protein x min)] was 19 in mouse, 17 in rat, and 14 in man and the apparent Km (mmol butadiene monoxide/l incubate) was 1.5 in mouse. 0.7 in rat, and 0.5 in man. Glutathione S-transferase activity was found in cytosol only, revealing first order kinetics in the measured range. The ratio Vmax/Km [(nmol butadiene monoxide x 1)/(mg protein x min x mmol of butadiene monoxide)] was 15 in mouse, 11 in rat, and 8 in man. The data obtained were used to extrapolate on the total rate of butadiene monoxide metabolism for each species in vivo: it was calculated to be 1.3 times higher in mice and 2.3 times lower in man compared to rats, when corrected for body weight.
AuthorsP E Kreuzer, W Kessler, H F Welter, C Baur, J G Filser
JournalArchives of toxicology (Arch Toxicol) Vol. 65 Issue 1 Pg. 59-67 ( 1991) ISSN: 0340-5761 [Print] Germany
PMID2043052 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Epoxy Compounds
  • 3,4-epoxy-1-butene
Topics
  • Animals
  • Chromatography, Gas
  • Cytosol (metabolism)
  • Epoxy Compounds (pharmacokinetics)
  • Humans
  • In Vitro Techniques
  • Liver (metabolism)
  • Male
  • Mice
  • Microsomes, Liver (metabolism)
  • Rats
  • Rats, Inbred Strains
  • Species Specificity

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