MS-based targeted metabolomics of eicosanoids and other oxylipins: Analytical and inter-individual variabilities

被引:62
作者
Gladine, Cecile [1 ]
Ostermann, Annika I. [2 ]
Newman, John W. [3 ,4 ]
Schebb, Nils Helge [2 ]
机构
[1] Univ Clermont Auvergne, INRA, UNH, CRNH Auvergne, Clermont Ferrand, France
[2] Univ Wuppertal, Fac Math & Nat Sci, Chair Food Chem, Gaussstr 20, D-42119 Wuppertal, Germany
[3] ARS, USDA, Western Human Nutr Res Ctr, Davis, CA USA
[4] Univ Calif Davis, Dept Nutr, Davis, CA 95616 USA
关键词
POLYUNSATURATED FATTY-ACIDS; SOLUBLE EPOXIDE HYDROLASE; TANDEM MASS-SPECTROMETRY; PERFORMANCE LIQUID-CHROMATOGRAPHY; VIRGIN OLIVE OIL; ARACHIDONIC-ACID; DOCOSAHEXAENOIC ACID; HUMAN PLASMA; LC-MS/MS; EPOXYEICOSATRIENOIC ACIDS;
D O I
10.1016/j.freeradbiomed.2019.05.012
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
Oxylipins, including the well-known eicosanoids, are potent lipid mediators involved in numerous physiological and pathological processes. Therefore, their quantitative profiling has gained a lot of attention during the last years notably in the active field of health biomarker discovery. Oxylipins include hundreds of structurally and stereochemically distinct lipid species which today are most commonly analyzed by (ultra) high performance liquid chromatography-mass spectrometry based ((U)HPLC-MS) methods. To maximize the utility of oxylipin profiling in clinical research, it is crucial to understand and assess the factors contributing to the analytical and biological variability of oxylipin profiles in humans. In this review, these factors and their impacts are summarized and discussed, providing a framework for recommendations expected to enhance the interlaboratory comparability and biological interpretation of oxylipin profiling in clinical research.
引用
收藏
页码:72 / 89
页数:18
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