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Identification of a novel conjugate in human urine: bile acid acyl galactosides
Authors:Goto Takaaki  Shibata Akihiro  Sasaki Daisuke  Suzuki Naoto  Hishinuma Takanori  Kakiyama Genta  Iida Takashi  Mano Nariyasu  Goto Junichi
Affiliation:Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Aoba-ku, Sendai 980-8578, Japan.
Abstract:We report a novel conjugate, bile acid acyl galactosides, which exist in the urine of healthy volunteers. To identify the two unknown peaks obtained in urine specimens from healthy subjects, the specimens were subjected to solid phase extraction and then to liquid chromatographic separation. The eluate corresponding to the unknown peaks on the chromatogram was collected. Following alkaline hydrolysis and liquid chromatography (LC)/electrospray ionization (ESI)-mass spectrometric (MS) analysis, cholic acid (CA) and deoxycholic acid (DCA) were identified as liberated bile acids. When a portion of the alkaline hydrolyzate was subjected to a derivatization reaction with 1-phenyl-3-methyl-5-pyrazolone, a derivative of galactose was detected by LC/ESI-MS. Finally, the liquid chromatographic and mass spectrometric properties of these unknown compounds in urine specimens were compared to those of authentic specimens and the structures were confirmed as CA 24-galactoside and DCA 24-galactoside. These results strongly imply that bile acid 24-galactosides, a novel conjugate, were synthesized in the human body.
Keywords:APCI, atmospheric pressure chemical ionization   CA, cholic acid   CDCA, chenodeoxycholic acid   DCA, deoxycholic acid   ESI, electrospray ionization   HDCA, hyodeoxycholic acid   LC, liquid chromatography   LCA, lithocholic acid   MS, mass spectrometry   MS/MS, tandem mass spectrometry   PMP, 3-methyl-1-phenyl-5-pyrazolone   Rks, relative retention factors   UGT, UDP-glucuronosyltransferase   UDCA, ursodeoxycholic acid
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