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  • 标题:Major urinary metabolites of 6-keto-prostaglandin F2α in mice
  • 本地全文:下载
  • 作者:Dmitry V. Kuklev ; Joseph A. Hankin ; Charis L. Uhlson
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2013
  • 卷号:54
  • 期号:7
  • 页码:1906-1914
  • DOI:10.1194/jlr.M037192
  • 语种:English
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:Western diets are enriched in omega-6 vs. omega-3 fatty acids, and a shift in this balance toward omega-3 fatty acids may have health benefits. There is limited information about the catabolism of 3-series prostaglandins (PG) formed from eicosapentaenoic acid (EPA), a fish oil omega-3 fatty acid that becomes elevated in tissues following fish oil consumption. Quantification of appropriate urinary 3-series PG metabolites could be used for noninvasive measurement of omega-3 fatty acid tone. Here we describe the preparation of tritium- and deuterium-labeled 6-keto-PGF and their use in identifying urinary metabolites in mice using LC-MS/MS. The major 6-keto-PGF urinary metabolites included dinor-6-keto-PGF (∼10%) and dinor-13,14-dihydro-6,15-diketo-PGF (∼10%). These metabolites can arise only from the enzymatic conversion of EPA to the 3-series PGH endoperoxide by cyclooxygenases, then PGI3 by prostacyclin synthase and, finally, nonenzymatic hydrolysis to 6-keto-PGF. The 6-keto-PGF derivatives are not formed by free radical mechanisms that generate isoprostanes, and thus, these metabolites provide an unbiased marker for utilization of EPA by cyclooxygenases.
  • 关键词:fish oil ; eicosapentaenoic acid ; prostacyclin ; cyclooxygenase
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