
The study aimed to investigate the potential of zebrafish in imitating mammal phase I metabolism of natural compounds. Three diterpenoid quinones from Radix Salvia miltiorrhiza, namely tanshinone IIA (TIIA), cryptotanshinone (Cry) and tanshinone I (TI) were selected as model compounds, and their metabolites mediated by zebrafish were characterized using a high-performance liquid chromatography coupled ion-trap mass spectrometry (HPLC/IT-MSn) method with electrospray ionization in positive mode. The separation was performed with a Zorbax C-18 column using a binary gradient elution of 0.05% formic acid acetonitrile/0.05% formic acid water. According to the MS spectra and after comparison with reference standards and literature reports, hydroxylation, dehydrogenation or D-ring hydrolysis metabolites of TIIA and Cry but not of TI were characterized, which coincided with those reported using regular in vivo or in vitro metabolic analysis methods, thus verifying that zebrafish can successfully imitate mammalian phase I metabolism which instills further confidence in using zebrafish as a novel and prospective metabolism model.
zebrafish; phase I metabolism; tanshinone IIA; cryptotanshinone; tanshinone I; Radix Salvia miltiorrhiza, Organic chemistry, Salvia miltiorrhiza, Phenanthrenes, zebrafish, tanshinone IIA, Article, cryptotanshinone, tanshinone I, QD241-441, Radix Salvia miltiorrhiza, Abietanes, phase I metabolism, Animals, Metabolic Networks and Pathways, Zebrafish, Drugs, Chinese Herbal
zebrafish; phase I metabolism; tanshinone IIA; cryptotanshinone; tanshinone I; Radix Salvia miltiorrhiza, Organic chemistry, Salvia miltiorrhiza, Phenanthrenes, zebrafish, tanshinone IIA, Article, cryptotanshinone, tanshinone I, QD241-441, Radix Salvia miltiorrhiza, Abietanes, phase I metabolism, Animals, Metabolic Networks and Pathways, Zebrafish, Drugs, Chinese Herbal
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