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首页> 外文期刊>Biochimica et Biophysica Acta. Molecular and cell biology of Lipids >Oxidized and nitrated oleic acid in biological systems: analysis by GC-MS/MS and LC-MS/MS, and biological significance.
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Oxidized and nitrated oleic acid in biological systems: analysis by GC-MS/MS and LC-MS/MS, and biological significance.

机译:生物系统中的氧化和硝化油酸:通过GC-MS / MS和LC-MS / MS进行分析以及生物学意义。

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摘要

Compared to the arachidonic acid (C20:4) cascade, the oleic acid (C18:1) family comprises a handful known metabolites. The pathophysiology of oleic acid and its oxidized and nitrated metabolites, i.e., cis-9,10-epoxyoctadecanoic acid (cis-EpOA) and the two vinylic nitro-oleic acids cis-9-nitro-oleic acid (9-NO(2)-OA) and cis-10-nitro-oleic acid (10-NO(2)-OA), is only little investigated and little understood. cis-EpOA, 9-NO(2)-OA and 10-NO(2)-OA have been detected in plasma of healthy and ill human subjects by means of gas chromatography-tandem mass spectrometry (GC-MS/MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) techniques in their acid and esterified forms. cis-EpOA is formed from oleic acid by the catalytic action of various cytochrome P450 isozymes. In end-stage liver disease, cis-EpOA plasma concentration is lower than in healthy subjects suggesting liver as the main organ responsible for cis-EpOA synthesis. The origin of 9-NO(2)-OA and 10-NO(2)-OA and of other nitrated oleic acid metabolites is unknown. In vitro models, nitro-oleic acid species can be formed non-enzymatically from oleic acid and nitrogen dioxide. Thus, endogenous nitro-oleic acids could serve as biomarkers of fatty acid nitration by reactive nitrogen species. Synthetic 9-NO(2)-OA and 10-NO(2)-OA at concentrations of three orders of magnitude higher than their endogenous counterparts have interesting pharmacological features and are currently intensely investigated. The present article reviews and discusses currently available analytical methods for the quantitative determination of cis-EpOA, 9-NO(2)-OA and 10-NO(2)-OA in biological samples, notably in human plasma, and the potential biological significance of these oleic acid metabolites. Special emphasis is given to GC-MS/MS and LC-MS/MS methods utilizing the stable-isotope dilution technique. The sensitivity and specificity of the MS/MS approach make electron-capture negative ion chemical ionization (ECNICI) GC-MS/MS and negative electrospray ionization (NESI) LC-MS/MS methodologies indispensable in experimental and clinical settings on oxidative and nitrative oleic acid metabolism. These techniques are particularly suited to delineate the oleic acid cascade.
机译:与花生四烯酸(C20:4)级联相比,油酸(C18:1)家族包含一些已知的代谢产物。油酸及其氧化和硝化代谢产物即cis-9,10-环氧十八碳烯酸(cis-EpOA)和两个乙烯基硝基-油酸cis-9-硝基-油酸(9-NO(2))的病理生理-OA)和顺式-10-硝基油酸(10-NO(2)-OA),只有很少的研究和了解。通过气相色谱-串联质谱法(GC-MS / MS)和液体在健康和患病人群的血浆中检测到了顺式-EpOA,9-NO(2)-OA和10-NO(2)-OA酸和酯化形式的色谱-串联质谱(LC-MS / MS)技术。顺式-EpOA由油酸通过各种细胞色素P450同工酶的催化作用形成。在终末期肝病中,顺式-EpOA血浆浓度低于健康受试者,表明肝脏是负责顺式-EpOA合成的主要器官。 9-NO(2)-OA和10-NO(2)-OA以及其他硝化油酸代谢产物的来源尚不清楚。在体外模型中,硝基油酸物质可以由油酸和二氧化氮非酶法形成。因此,内源性硝基油酸可作为通过反应性氮物种进行脂肪酸硝化的生物标志物。合成的9-NO(2)-OA和10-NO(2)-OA的浓度比其内源对应物高三个数量级,具有令人感兴趣的药理特性,目前正在深入研究。本文回顾并讨论了目前可用的定量分析生物样品中,尤其是人体血浆中的顺式-EpOA,9-NO(2)-OA和10-NO(2)-OA的分析方法,以及潜在的生物学意义这些油酸代谢产物。特别强调了利用稳定同位素稀释技术的GC-MS / MS和LC-MS / MS方法。 MS / MS方法的灵敏度和特异性使得电子捕获负离子化学电离(ECNICI)GC-MS / MS和负电喷雾电离(NESI)LC-MS / MS方法在氧化和硝化油酸的实验和临床环境中必不可少酸代谢。这些技术特别适合于描绘油酸级联。

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