Measurement of F2- isoprostanes and isofurans using gas chromatography-mass spectrometry

被引:90
作者
Milne, Ginger L. [1 ,2 ]
Gao, Benlian [1 ,2 ]
Terry, Erin S. [1 ,2 ]
Zackert, William E. [2 ]
Sanchez, Stephanie C. [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Eicosanoid Core Lab, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Div Clin Pharmacol, Nashville, TN 37232 USA
关键词
Methods; Lipid oxidation; Isoprostanes; Oxidative stress; Mass spectrometry; OXIDATIVE STRESS; NOMENCLATURE SYSTEM; LIPID-PEROXIDATION; HUMAN URINE; IN-VIVO; F-2-ISOPROSTANES; PRODUCTS; HUMANS; OXYGEN; QUANTIFICATION;
D O I
10.1016/j.freeradbiomed.2012.09.030
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
F-2-Isoprostanes (IsoPs) are isomers of prostaglandin F-2 alpha formed from the nonenzymatic free radical-catalyzed peroxidation of arachidonic acid. Since discovery of these molecules by Morrow and Roberts in 1990, F-2-IsoPs have been shown to be excellent biomarkers as well as potent mediators of oxidative stress in vivo in humans. Isofurans (IsoFs) are also oxidation products generated from the nonenzymatic oxidation of arachidonic acid. IsoFs are preferentially formed instead of F-2-IsoPs in settings of increased oxygen tension. The protocol presented herein is the current methodology that our laboratory uses to quantify F-2-IsoPs and IsoFs in biological tissues and fluids using gas chromatography/mass spectrometry (GC/MS). A variety of analytical procedures to measure F-2-IsoPs, including other GC/MS methods and liquid chromatography/MS and immunological approaches, are reported in the literature. This method provides a very low limit of quantitation and is suitable for analysis of both F-2-IsoPs and IsoFs from a variety of biological sources including urine, plasma, tissues, cerebral spinal fluid, exhaled breath condensate, and amniotic fluid, among others. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:36 / 44
页数:9
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