Identification of a novel conjugate in human urine: bile acid acyl galactosides |
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Authors: | Goto Takaaki Shibata Akihiro Sasaki Daisuke Suzuki Naoto Hishinuma Takanori Kakiyama Genta Iida Takashi Mano Nariyasu Goto Junichi |
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Affiliation: | Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Aoba-ku, Sendai 980-8578, Japan. |
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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. |
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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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