Isoprostane levels in lipids extracted from atherosclerotic arteries of nonhuman primates |
| |
Authors: | Thomas M J Chen Q Sorci-Thomas M G Rudel L L |
| |
Institution: | * Department of Biochemistry, Wake Forest University School of Medicine, Winston-Salem, NC, USA † Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC, USA |
| |
Abstract: | Nonhuman primates used in these studies had been fed for 5 years diets enriched with cholesterol and one of three classes of fatty acids: saturated, monounsaturated, or polyunsaturated fatty acids. Atherosclerotic iliac artery lipid extracts were quantitatively analyzed for cholesterol, cholesteryl esters, fatty acid composition, and a marker of lipid oxidation, the F2-isoprostanes. There was no significant difference in the mean accumulation of F2-isoprostanes among the different diet groups. To account for the small, individual variation in the arachidonate concentration the F2-isoprostane mass from each sample was normalized by dividing by arachidonate mass: F2-isoprostane mass/(mass arachidonate). At lower levels of cholesterol accumulation, the F2-isoprostane mass/(mass arachidonate) ratio was greater in lipids from POLY arteries compared to SAT arteries, but the reverse was true at high levels of cholesterol. F2-isoprostane/(mass arachidonate) increased with mole fraction linoleate for the SAT group, but decreased for the POLY group. In summary, these studies demonstrated that there is no simple explanation of how F2-isoprostane accumulation did not depend on the concentration of oxidizable lipids that promote free-radical lipid oxidation. |
| |
Keywords: | Atherosclerosis Dietary fatty acids Free radical autoxidation F2-isoprostane Lipids Free radicals |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|