http://www.cnr.it/ontology/cnr/individuo/prodotto/ID37416
Identification of metabolites from type III F2-isoprostane diastereoisomers by mass spectrometry. (Articolo in rivista)
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- Label
- Identification of metabolites from type III F2-isoprostane diastereoisomers by mass spectrometry. (Articolo in rivista) (literal)
- Anno
- 2002-01-01T00:00:00+01:00 (literal)
- Alternative label
Chiabrando C., Rivalta C., Bagnati R., Valagussa A., Durand T., Guy A., Villa P., Rossi J.C., Fanelli R. (2002)
Identification of metabolites from type III F2-isoprostane diastereoisomers by mass spectrometry.
in Journal of lipid research (Print)
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- Chiabrando C., Rivalta C., Bagnati R., Valagussa A., Durand T., Guy A., Villa P., Rossi J.C., Fanelli R. (literal)
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- ISI Web of Science (WOS) (literal)
- Titolo
- Identification of metabolites from type III F2-isoprostane diastereoisomers by mass spectrometry. (literal)
- Abstract
- F(2)-isoprostanes (F(2)-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 F(2)-iPs in vivo is still scant,
despite its importance for defining their overall formation and
biological effects in vivo. Type III F(2)-iPs, which are
diastereoisomers of cyclooxygenase-derived PGF(2alpha), may be
metabolized through the pathways of PG metabolism. We therefore
studied the in vitro metabolism of eight synthetic Type III F(2)-iP
diastereoisomers in comparison with PGF(2alpha). 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. PGF(2alpha) was
metabolized to several known products, resulting from a combination
of beta-oxidation, reduction of Delta(5) and/or Delta(13) double
bonds, and 15-OH oxidation, plus other novel products deriving from
conjugation with taurine of PGF(2alpha) and its metabolites. Of the
eight F(2)-iP diastereoisomers, some were processed similarly to
PGF(2alpha), whereas others showed peculiar metabolic profiles
according to specific stereochemical configurations.These data
represent the first evidence of biodegradation of selected Type III
F(2)-iP isomers other than 8-epi-PGF(2alpha), through known and
novel pathways of PGF(2alpha) metabolism. The analytical
characterization of these products may serve as a basis for
identifying the most significant products formed in vivo. (literal)
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