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.
|
Authors | P E Kreuzer, W Kessler, H F Welter, C Baur, J G Filser |
Journal | Archives of toxicology
(Arch Toxicol)
Vol. 65
Issue 1
Pg. 59-67
( 1991)
ISSN: 0340-5761 [Print] Germany |
PMID | 2043052
(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
|