出版社：American Society for Biochemistry and Molecular Biology
摘要：F2-isoprostanes (F2-iPs) are prostaglandin (PG)-like products of non-enzymatic free radical-catalyzed peroxidation of arachidonic acid that are now widely used as indices of lipid peroxidation in vivo. Knowledge of the metabolic fate of F2-iPs in vivo is still scant, despite its importance for defining their overall formation and biological effects in vivo. Type III F2-iPs, which are diastereoisomers of cyclooxygenase-derived PGF2α, may be metabolized through the pathways of PG metabolism. We therefore studied the in vitro metabolism of eight synthetic Type III F2-iP diastereoisomers in comparison with PGF2α. We used gas chromatography-mass spectrometry and high performance liquid chromatography-electrospray-tandem mass spectrometry for structural identification of metabolites formed after incubation of the various compounds with isolated rat hepatocytes. PGF2α was metabolized to several known products, resulting from a combination of β-oxidation, reduction of Δ5 and/or Δ13 double bonds, and 15-OH oxidation, plus other novel products deriving from conjugation with taurine of PGF2α and its metabolites. Of the eight F2-iP diastereoisomers, some were processed similarly to PGF2α, whereas others showed peculiar metabolic profiles according to specific stereochemical configurations. These data represent the first evidence of biodegradation of selected Type III F2-iP isomers other than 8- epi -PGF2α, through known and novel pathways of PGF2α metabolism. The analytical characterization of these products may serve as a basis for identifying the most significant products formed in vivo. —Chiabrando, C., C. Rivalta, R. Bagnati, A. Valagussa, T. Durand, A. Guy, P. Villa, J-C. Rossi, and R. Fanelli. Identification of metabolites from Type III F2-isoprostane diastereoisomers by mass spectrometry. J. Lipid Res. 2002. 43: 495–509.
关键词：PGF2α ; taurine conjugation ; isolated rat hepatocytes ; gas chromatography-mass spectrometry ; high performance liquid chromatography-electrospray-tandem mass spectrometry
