Journal
JOURNAL OF LIPID RESEARCH
Volume 50, Issue 4, Pages 716-722Publisher
ELSEVIER
DOI: 10.1194/jlr.M800607-JLR200
Keywords
HDL oxidation; oxidatively damaged lipid; PAF-AH; PON-1; FPLC
Categories
Funding
- National Heart Foundation of Australia
- National Health and Medical Research Council of Australia
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Enhanced oxidative stress is implicated in the development of atherosclerosis in humans and animal models. F-2-isoprostanes are formed in vivo via free radical peroxidation of arachidonic acid, and their quantification has allowed assessment of oxidative stress in vivo. F-2-isoprostanes associate with lipids, although their distribution in human plasma lipoproteins is unknown. Our aim was to determine the distribution and levels of F-2-isoprostanes in lipoproteins isolated from human plasma by ultracentrifugation and fast protein liquid chromatography (FPLC). F-2-isoprostanes were significantly higher in HDL compared with LDL or VLDL after isolation by ultracentrifugation or FPLC. Furthermore, HDL3 particles contained elevated levels of F-2-isoprostanes compared with HDL2. Platelet activating factor acetylhydrolase (PAF-AH), which hydrolyses esterified F-2-isoprostanes from phospholipids, was predominantly associated with LDL. Reduced F-2-isoprostanes in LDL may be related to higher PAF-AH activity in LDL. Paraoxonase 1 (PON-1) activity was associated with HDL2 and may be a contributing factor to the lower F-2-isoprostanes in HDL2 compared with HDL3. Further studies are required to establish the implications of these findings on HDL function.-Proudfoot, J. M., A. E. Barden, W. M. Loke, K. D. Croft, I. B. Puddey, and T. A. Maori. HDL is the major lipoprotein carrier of plasma F-2-isoprostanes. J. Lipid Res. 2009. 50: 716-722.
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