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使用液相色谱-质谱联用技术对生物活性花生四烯酸代谢物进行靶向手性分析。

Targeted chiral analysis of bioactive arachidonic Acid metabolites using liquid-chromatography-mass spectrometry.

作者信息

Mesaros Clementina, Blair Ian A

机构信息

Centers for Cancer Pharmacology and Excellence in Environmental Toxicology, Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

出版信息

Metabolites. 2012 Apr 20;2(2):337-65. doi: 10.3390/metabo2020337.

Abstract

A complex structurally diverse series of eicosanoids arises from the metabolism of arachidonic acid. The metabolic profile is further complicated by the enantioselectivity of eicosanoid formation and the variety of regioisomers that arise. In order to investigate the metabolism of arachidonic acid in vitro or in vivo, targeted methods are advantageous in order to distinguish between the complex isomeric mixtures that can arise by different metabolic pathways. Over the last several years this targeted approach has become more popular, although there are still relatively few examples where chiral targeted approaches have been employed to directly analyze complex enantiomeric mixtures. To efficiently conduct targeted eicosanoid analyses, LC separations are coupled with collision induced dissociation (CID) and tandem mass spectrometry (MS/MS). Product ion profiles are often diagnostic for particular regioisomers. The highest sensitivity that can be achieved involves the use of selected reaction monitoring/mass spectrometry (SRM/MS); whereas the highest specificity is obtained with an SRM transitions between an intense parent ion, which contains the intact molecule (M) and a structurally significant product ion. This review article provides an overview of arachidonic acid metabolism and targeted chiral methods that have been utilized for the analysis of the structurally diverse eicosanoids that arise.

摘要

一系列结构复杂多样的类二十烷酸源自花生四烯酸的代谢。类二十烷酸形成过程中的对映选择性以及产生的多种区域异构体,使得代谢谱更加复杂。为了在体外或体内研究花生四烯酸的代谢,靶向方法有助于区分由不同代谢途径产生的复杂异构体混合物。在过去几年中,这种靶向方法越来越受欢迎,尽管采用手性靶向方法直接分析复杂对映体混合物的例子仍然相对较少。为了有效地进行靶向类二十烷酸分析,液相色谱分离与碰撞诱导解离(CID)和串联质谱(MS/MS)联用。产物离子谱通常对特定的区域异构体具有诊断性。可实现的最高灵敏度涉及使用选择反应监测/质谱(SRM/MS);而最高特异性则通过在含有完整分子(M)的强母离子与结构上有意义的产物离子之间进行SRM跃迁获得。这篇综述文章概述了花生四烯酸代谢以及用于分析所产生的结构多样的类二十烷酸的靶向手性方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1576/3901208/d8b1960d672d/metabolites-02-00337-g001.jpg

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本文引用的文献

3
Epoxyeicosanoids stimulate multiorgan metastasis and tumor dormancy escape in mice.
J Clin Invest. 2012 Jan;122(1):178-91. doi: 10.1172/JCI58128. Epub 2011 Dec 19.
4
Epoxyeicosatrienoic acids: a double-edged sword in cardiovascular diseases and cancer.
J Clin Invest. 2012 Jan;122(1):19-22. doi: 10.1172/JCI61453. Epub 2011 Dec 19.
5
Metabolomics-lipidomics of eicosanoids and docosanoids generated by phagocytes.
Curr Protoc Immunol. 2011 Nov;Chapter 14:Unit 14.26. doi: 10.1002/0471142735.im1426s95.
6
Hepoxilins in cancer and inflammation--use of hepoxilin antagonists.
Cancer Metastasis Rev. 2011 Dec;30(3-4):493-506. doi: 10.1007/s10555-011-9307-y.
7
LOX-1, oxidative stress and inflammation: a novel mechanism for diabetic cardiovascular complications.
Cardiovasc Drugs Ther. 2011 Oct;25(5):451-9. doi: 10.1007/s10557-011-6342-4.
8
11-Oxoeicosatetraenoic acid is a cyclooxygenase-2/15-hydroxyprostaglandin dehydrogenase-derived antiproliferative eicosanoid.
Chem Res Toxicol. 2011 Dec 19;24(12):2227-36. doi: 10.1021/tx200336f. Epub 2011 Sep 30.
9
Tumor-associated macrophages mediate immunosuppression in the renal cancer microenvironment by activating the 15-lipoxygenase-2 pathway.
Cancer Res. 2011 Oct 15;71(20):6400-9. doi: 10.1158/0008-5472.CAN-11-1261. Epub 2011 Sep 7.
10
Regulation of inflammation in cancer by eicosanoids.
Prostaglandins Other Lipid Mediat. 2011 Nov;96(1-4):27-36. doi: 10.1016/j.prostaglandins.2011.08.004. Epub 2011 Aug 16.

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