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Curr Protoc Toxicol. 2011 Feb 1;Chapter 17:Unit17.14.2. doi: 10.1002/0471140856.tx1714s45.

LC-MS/MS quantitation of mercapturic acid conjugates of lipid peroxidation products as markers of oxidative stress.

Author information

  • 1Linus Pauling Institute and the Department of Pharmaceutical Sciences, Oregon State University, Corvallis, Oregon, USA. hkuiper@email.unc.edu

Abstract

Oxidative stress-induced lipid peroxidation (LPO) leads to the formation of cytotoxic and genotoxic 2-alkenals. LPO products such as 4-hydroxy-2(E)-nonenal (HNE) and 4-oxo-2(E)-nonenal (ONE) have been the subject of many studies due to their association with the development of cardiovascular and neurodegenerative diseases, as well as cancer. LPO products are excreted in the urine after conjugation with glutathione (GSH) and subsequent metabolism to mercapturic acid (MA) conjugates. Urinary LPO-MA metabolites are stable end-product metabolites and have gained interest as non-invasive in vivo biomarkers of oxidative stress. This protocol describes a method for the quantitative analysis of LPO-MA metabolites in urine using isotope-dilution liquid chromatography coupled with electrospray tandem mass spectrometry (LC-MS/MS). Included are protocols for preparation of labeled LPO-MA conjugates from unlabeled LPO products and deuterium labeled MA.

KEYWORDS:

lipid peroxidation; mass spectrometry; mercapturic acid; oxidative stress

PMID:
21442005
[PubMed - indexed for MEDLINE]
PMCID:
PMC3062851
Free PMC Article

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Figure 17.14.1
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Figure 17.14.3
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