Abstract

Doc number: 24

Abstract

Background: Lipidomic analysis was performed to explore differences in lipid profiles between plasma from lean and obese subjects, followed by in vitro methods to examine a role for the identified lipids in endothelial cell pathophysiology.

Methods: Plasma was collected from 15 morbidly obese and 13 control subjects. Lipids were extracted from plasma and analyzed using LC/MS, and MS/MS to characterize lipid profiles and identify lipids that are elevated in obese subjects compared to lean.

Results: Orthogonal partial least squares-discriminant analysis (OPLS-DA) modelling showed that lipid profiles were significantly different in obese subjects compared to lean. Analysis of lipids that were driving group separation in the OPLS-DA model and that were significantly elevated in the obese group led to identification of a group of ether-linked phosphatidylcholine (PC) and phosphatidylethanolamine (PE) lipids of interest. Treatment of human coronary artery endothelial cells with the ether-linked phosphatidylethanolamine induced expression of cell adhesion molecules, a hallmark of endothelial cell activation. However, oxidized phosphatidylcholine products that can induce endothelial cell activation in vitro , were not significantly different between groups in vivo .

Conclusion: These data suggest a role for ether-linked lipids in obesity associated dyslipidemia and vascular disease.

Details

Title
Lipidomic analysis of human plasma reveals ether-linked lipids that are elevated in morbidly obese humans compared to lean
Author
Donovan, Elise L; Pettine, Stefan M; Hickey, Matthew S; Hamilton, Karyn L; Miller, Benjamin F
Publication year
2013
Publication date
2013
Publisher
BioMed Central
e-ISSN
1758-5996
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1356067763
Copyright
© 2013 Donovan et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.