Liquid Chromatography-Mass Spectrometry-Based In Vitro Metabolic Profiling Reveals Altered Enzyme Expressions in Eicosanoid Metabolism

被引:2
|
作者
Lee, Su Hyeon [1 ,2 ]
Kim, Eung Ju [3 ]
Lee, Dong-Hyoung [1 ]
Lee, Won-Yong [2 ]
Chung, Bong Chul [1 ]
Seo, Hong Seog [3 ]
Choi, Man Ho [1 ]
机构
[1] Korea Inst Sci & Technol, Mat & Life Sci Res Div, 5 Hwarang Ro 14 Gil, Seoul 02792, South Korea
[2] Yonsei Univ, Dept Chem, Seoul 120749, South Korea
[3] Korea Univ, Guro Hosp, Cardiovasc Ctr, 148 Gurodong Ro, Seoul 08308, South Korea
关键词
Eicosanoids; Arachidonic acid; Liquid chromatography-mass spectrometry; Liver S9 fraction; Epitestosterone; LC-MS/MS; INFLAMMATION; TESTOSTERONE; DEHYDROEPIANDROSTERONE; EPITESTOSTERONE; LIPIDOMICS; OXYLIPINS; MEDIATORS; CYTOKINES;
D O I
10.3343/alm.2016.36.4.342
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Eicosanoids are metabolites of arachidonic acid that are rapidly biosynthesized and degraded during inflammation, and their metabolic changes reveal altered enzyme expression following drug treatment. We developed an eicosanoid profiling method and evaluated their changes on drug treatment. Methods: Simultaneous quantitative profiling of 32 eicosanoids in liver S9 fractions obtained from rabbits with carrageenan-induced inflammation was performed and validated by liquid chromatography-mass spectrometry coupled to anion-exchange solid-phase purification. Results: The limit of quantification for the devised method ranged from 0.5 to 20.0 ng/mg protein, and calibration linearity was achieved (R-2>0.99). The precision (% CV) and accuracy (% bias) ranged from 4.7 to 10.3% and 88.4 to 110.9%, respectively, and overall recoveries ranged from 58.0 to 105.3%. Our method was then applied and showed that epitestosterone treatment reduced the levels of all eicosanoids that were generated by cyclooxygenases and lipoxygenases. Conclusions: Quantitative eicosanoid profiling combined with in vitro metabolic assays may be useful for evaluating metabolic changes affected by drugs during eicosanoid metabolism.
引用
收藏
页码:342 / 352
页数:11
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