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Identification of two major F2 isoprostanes, 8,12-iso- and 5-epi-8,12-iso-isoprostane F2α-VI, in human urine
被引:74
作者:
Lawson, JA
Li, HW
Rokach, J
Adiyaman, M
Hwang, SW
Khanapure, SP
FitzGerald, GA
[1
]
机构:
[1] Univ Penn, Sch Med, Ctr Expt Therapeut, Stellar Chance Labs 905, Philadelphia, PA 19104 USA
[2] Florida Inst Technol, Claude Pepper Inst, Melbourne, FL 32901 USA
[3] Florida Inst Technol, Dept Chem, Melbourne, FL 32901 USA
关键词:
D O I:
10.1074/jbc.273.45.29295
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Isoprostanes (iPs) are nonenzymatic, free radical-derived compounds isomeric with enzymatically formed eicosanoids such as prostaglandins, leukotrienes, and thromboxanes. One group formed by the auto-oxidation of arachidonic acid, the F-2-iPs, consists of four classes of isomers of prostaglandin F-2 alpha (PGF(2 alpha)), They are relatively abundant in human urine. This fact, along with their chemical stability and excellent characteristics for quantitation by gas chromatography/mass spectrometry, has made them attractive indices of oxidative stress in humans. We developed a specific assay using gas chromatography/mass spectrometry for the first identified F-2-iP, iPF(2 alpha)-III (previously called 8-iso-PGF(2 alpha) or 8-epi-PGF(2 alpha)), which demonstrated the utility of monitoring a specific isomer, Recently, we described an assay for another isomer, iPF(2 alpha)-VI, which is present in urine in greater concentration than iPF(2 alpha)-III and which is particularly amenable to quantitation, We now describe the identification in human urine of two more isomers, 8,12-iso-iPF(2 alpha)-Vl and 5-epi-8,12-iso-iPF(2 alpha)-VI, using high performance liquid chromatography/tandem mass spectrometry and gas chromatography/mass spectrometry, These compounds are each present in similar to 5-fold greater concentrations than iPF(2 alpha)-VI (similar to 20-fold greater than iPF(2 alpha)-III), They share the unique chemical characteristics of class VI compounds, which make them attractive targets for quantitation by gas chromatography/mass spectrometry and immunoassay development.
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页码:29295 / 29301
页数:7
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