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Glutathione conjugation with the pyrrolizidine alkaloid, jacobine
S R Dueker1, M W Lamé, A D Jones
1Department of Veterinary Pharmacology and Toxicology, University of California, Davis 95616.
Biochemical and Biophysical Research Communications
|January 28, 1994
Abstract:
The reaction of glutathione with the epoxide containing pyrrolizidine alkaloid, jacobine, was catalyzed by guinea pig hepatic glutathione-S-transferase enzymes in in vitro experiments; the rate of the reaction in the presence of rat hepatic glutathione-S-transferases did not differ from the non-enzymatic rate. Using ion-pairing liquid chromatography we were able to isolate the conjugate and obtain a daughter ion spectrum using Fast Atom Bombardment Mass Spectrometry together with Collisionally Activated Dissociation/Mass Analyzed Kinetic Energy experiments.