Measurement of F2- isoprostanes and isofurans using gas chromatographyamp#x02013;mass spectrometry
نویسندگان
چکیده
F2-Isoprostanes (IsoPs) are isomers of prostaglandin F2a formed from the nonenzymatic free radicalcatalyzed peroxidation of arachidonic acid. Since discovery of these molecules by Morrow and Roberts in 1990, F2-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 F2-IsoPs in settings of increased oxygen tension. The protocol presented herein is the current methodology that our laboratory uses to quantify F2-IsoPs and IsoFs in biological tissues and fluids using gas chromatography/mass spectrometry (GC/MS). A variety of analytical procedures to measure F2-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 F2-IsoPs and IsoFs from a variety of biological sources including urine, plasma, tissues, cerebral spinal fluid, exhaled breath condensate, and amniotic fluid, among others. & 2012 Elsevier Inc. All rights reserved.
منابع مشابه
Association of plasma F2-isoprostanes and isofurans concentrations with erythropoiesis-stimulating agent resistance in maintenance hemodialysis patients
BACKGROUND In patients undergoing maintenance hemodialysis (HD), hyporesponsiveness to erythropoiesis stimulating agents (ESAs) is associated with adverse clinical outcomes. Systemic inflammation is highly prevalent in HD patients and is associated with ESA hyporesponsiveness. Oxidative stress is also highly prevalent in HD patients, but no previous study has determined its association with ESA...
متن کاملMethods of lipid oxidation product identification and quantification.
Lipid oxidation, both enzymatic and non-enzymatic, is involved in of nitrated fatty acid are provided. Sample extraction from comphysiological and pathological alteration of cell function. This special issue of Free Radical Biology & Medicine is devoted to the methods that can be used to identify and quantify the vast array of products of lipid oxidation. The issue however, begins with a review...
متن کاملMetabolomics approach to assessing plasma 13- and 9-hydroxy-octadecadienoic acid and linoleic acid metabolite responses to 75-km cycling.
Bioactive oxidized linoleic acid metabolites (OXLAMs) include 13- and 9-hydroxy-octadecadienoic acid (13-HODE + 9-HODE) and have been linked to oxidative stress, inflammation, and numerous pathological and physiological states. The purpose of this study was to measure changes in plasma 13-HODE + 9-HODE following a 75-km cycling bout and identify potential linkages to linoleate metabolism and es...
متن کاملAssessment of urinary F(2)-isoprostanes in experimental and clinical studies: mass spectrometry versus ELISA.
Assessment of Urinary F2-Isoprostanes in Experimental and Clinical Studies: Mass Spectrometry Versus ELISA To the Editor: Ojeda and colleagues reported that oxidative stress renal markers contribute to sex differences in blood pressure in adult growth-restricted offspring rats. The antibody used in the ELISA kit used by Ojeda et al isspecificfor15(S)-8-iso–PGF2 , 2 (http://www.oxfordbiomed.com/...
متن کاملAnalytical Variables Affecting Analysis of F2-Isoprostanes and F4-Neuroprostanes in Human Cerebrospinal Fluid by Gas Chromatography/Mass Spectrometry
F2-isoprostanes (F2-IsoPs) are a gold marker of lipid peroxidation in vivo, whereas F4-neuroprostanes (F4-NPs) measured in cerebrospinal fluid (CSF) or brain tissue selectively indicate neuronal oxidative damage. Gas chromatography/negative-ion chemical-ionization mass spectrometry (GC/NICI-MS) is the most sensitive and robust method for quantifying these compounds, which is essential for CSF s...
متن کامل