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Updated: Mar 13, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
F2-Isoprostanes in HDL are bound to neutral lipids and phospholipids
Julie M Proudfoot1, Anne E Barden1, Kevin D Croft1
1a School of Medicine and Pharmacology , University of Western Australia, Royal Perth Hospital Unit , Perth , Australia.
Insights
High-density lipoprotein (HDL) carries oxidized lipids, F2-isoprostanes (F2-IsoPs), in both neutral lipids and phospholipids. HDL-3 showed the highest F2-IsoP concentration, but specific molecular species in neutral lipids remain unconfirmed.
Area of Science:
- Lipid biochemistry
- Cardiovascular research
- Oxidative stress markers
Background:
- Low HDL cholesterol (HDL-C) is a risk factor for coronary artery disease (CAD), yet HDL-C-raising therapies have not reduced cardiovascular events.
- HDL is the primary carrier of plasma F2-isoprostanes (F2-IsoPs), markers of oxidative stress.
- While F2-IsoPs are typically linked to phospholipids, evidence suggests association with neutral lipids in rat liver.
Purpose of the Study:
- To identify lipid classes within human HDL containing F2-IsoPs.
- To investigate F2-IsoPs in both native and oxidized HDL particles.
- To determine if F2-IsoPs associate with neutral lipids in human HDL.
Main Methods:
- Analysis of lipid classes within HDL particles.
- In vitro oxidation of HDL.
- Targeted liquid chromatography-mass spectrometry (LC/MS) and high-resolution mass spectrometry (MS).
Main Results:
- F2-IsoPs were found to be bound to both neutral lipids and phospholipids within HDL.
- HDL-3 exhibited the highest F2-IsoP concentrations across all lipid classes, both before and after oxidation.
- Conclusive evidence for specific F2-isoprostane-cholesterol and F2-isoprostane-glycerol species in HDL neutral lipids was not obtained.
Conclusions:
- Oxidized lipids, including F2-IsoPs, are present in both the core and surface of HDL.
- The precise molecular identity of F2-IsoPs within HDL neutral lipids requires further characterization.
- Future research should explore the functional implications of F2-IsoPs in HDL neutral lipids on HDL function.
Abstract:
Low HDL cholesterol (HDL-C) is a risk factor for coronary artery disease (CAD). However, interventions that raise HDL-C have failed to reduce cardiovascular events. We previously reported that HDL is the main carrier of plasma F2-isoprostanes (F2-IsoPs) that are markers of oxidative stress formed upon oxidation of arachidonic acid. F2-IsoPs are predominantly associated with phospholipids. However, there is evidence that F2-IsoPs in the liver of rats treated with carbon tetrachloride associate with the neutral lipids. To date it is not known whether F2-IsoPs are found in the neutral lipids in HDL in humans. Possible candidate neutral lipids include cholesteryl esters, triglycerides, diglycerides, and monoglycerides. This study aimed to identify the lipid classes within native and oxidized HDL that contain F2-IsoPs. We showed that F2-IsoPs in HDL are bound to neutral lipids as well as phospholipids. HDL-3 contained the highest concentration of F2-IsoPs in all lipid classes before and after in vitro oxidation. Using targeted LC/MS and high resolution MS, we were unable to provide conclusive evidence for the presence of the synthesized standards 15(R)-15-F2t-isoP cholesterol and 1-ent-15(RS)-15-F2t-isoprostanoyl-sn-glycerol in the neutral lipids of HDL. Our findings show that oxidized lipids such as F2-IsoPs are found in the core and surface of HDL. However, the exact molecular species remain to be definitively characterized. Future studies are required to determine whether the presence of F2-IsoPs in neutral lipids alters HDL function.
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