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1.
Anal Chim Acta ; 651(1): 69-74, 2009 Sep 28.
Artigo em Inglês | MEDLINE | ID: mdl-19733737

RESUMO

Neurosteroid glucuronides were found for the first time in brain samples. The intact glucuronides were extracted from the cortex, hippocampus, hypothalamus, and mid-brain tissues of nicotine- and water-treated mice, and detected with capillary liquid chromatography-electrospray-tandem mass spectrometry (CapLC-ESI-MS/MS). The glucuronides of estradiol, cortisol, corticosterone, tetrahydrodeoxycorticosterone, pregnenolone, and isopregnanolone were identified by comparing retention times in selected reaction monitoring (SRM) chromatograms and the relative abundances of two SRM transitions of each neurosteroid glucuronide between the reference and authentic samples, thus providing reliable identification. In vitro experiments, carried out by using S9 fractions from mouse and rat brains, showed a formation of glucuronides with selected test compounds (corticosterone, pregnenolone, and dehydroepiandrosterone), suggesting that biosynthesis of neurosteroid glucuronides is possible in rodent brain.


Assuntos
Encéfalo/metabolismo , Glucuronídeos/análise , Animais , Cromatografia Líquida de Alta Pressão , Corticosterona/análise , Desidroepiandrosterona/análise , Glucuronídeos/isolamento & purificação , Masculino , Camundongos , Pregnenolona/análise , Ratos , Espectrometria de Massas em Tandem
2.
Bioorg Chem ; 36(3): 148-55, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-18378273

RESUMO

Three angiotensin II receptor antagonists--losartan, candesartan, and zolarsartan--were investigated. All the compounds, which are structural analogues, are metabolized via conjugation to glucuronic acid. Interestingly, both O- and N-glucuronidation take place, so that regioisomers are formed. One ether O-glucuronide, two acyl O-glucuronides, and five tetrazole-N-glucuronides were biosynthesized, in milligram scale, from the three sartan aglycones. Liver microsomes from bovine, moose, rat, and pig and recombinant human UDP-glucuronosyltransferases were used as catalysts. The synthesized compounds were identified as sartan glucuronides by mass spectrometry, while the sites of glucuronidation were determined by nuclear magnetic resonance spectroscopy. Drug metabolites are needed as standards for pharmaceutical research and, as the present study shows, they can easily be produced with enzymes as catalyst.


Assuntos
Bloqueadores do Receptor Tipo 1 de Angiotensina II/síntese química , Antagonistas de Receptores de Angiotensina , Glucuronídeos/farmacologia , Animais , Benzimidazóis , Compostos de Bifenilo , Bovinos , Cervos , Ácido Glucurônico , Glucuronídeos/síntese química , Glucuronosiltransferase/metabolismo , Humanos , Losartan , Espectroscopia de Ressonância Magnética , Espectrometria de Massas , Microssomos Hepáticos/metabolismo , Ratos , Suínos , Tetrazóis
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