2015
DOI: 10.1016/j.bbamem.2014.10.016
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Eicosapentaenoic acid inhibits glucose-induced membrane cholesterol crystalline domain formation through a potent antioxidant mechanism

Abstract: Lipid oxidation leads to endothelial dysfunction, inflammation, and foam cell formation during atherogenesis. Glucose also contributes to lipid oxidation and promotes pathologic changes in membrane structural organization, including the development of cholesterol crystalline domains. In this study, we tested the comparative effects of eicosapentaenoic acid (EPA), an omega-3 fatty acid indicated for the treatment of very high triglyceride (TG) levels, and other TG-lowering agents (fenofibrate, niacin, and gemfi… Show more

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Cited by 65 publications
(67 citation statements)
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“…When mice were fed the leather carp extract, blood glucose levels increased to near hyperglycemic levels. It is known that hyperglycemia may change the organization of membrane lipids, which is correlated with increased formation of lipid hydroperoxide (LOOH), an intermediate product of oxidative lipid damage (30). Leather carp extract also increased GPx and SOD antioxidant activities in the blood, which may help protect against oxidative lipid damage.…”
Section: Resultsmentioning
confidence: 99%
“…When mice were fed the leather carp extract, blood glucose levels increased to near hyperglycemic levels. It is known that hyperglycemia may change the organization of membrane lipids, which is correlated with increased formation of lipid hydroperoxide (LOOH), an intermediate product of oxidative lipid damage (30). Leather carp extract also increased GPx and SOD antioxidant activities in the blood, which may help protect against oxidative lipid damage.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, EPA has been associated with decreased expression of genes involved in the NF-κB pathway [28]. Other antiatherosclerotic mechanisms of EPA include antioxidant effects of EPA in both lipoproteins and cell membranes, including the inhibition of cholesterol crystalline domains [18,[29][30][31]. Beneficial effects of EPA on atherosclerotic plaque have been demonstrated in preclinical studies as well as multiple clinical studies and are described in more detail in the next section.…”
Section: Pleiotropic Effects Of Epa In the Atherosclerotic Pathwaymentioning
confidence: 99%
“…EPA has been shown to increase the levels of nitric oxide and improve endothelial and vascular function [14,[16][17][18] and have beneficial effects on monocytes and macrophages, including decreased adhesion of monocytes, decreased macrophage accumulation, and decreased foam cell accumulation [19][20][21][22]. Anti-inflammatory effects of EPA include beneficial modulation of pro-and anti-inflammatory cytokine levels [23,24] and reduction of high-sensitivity C-reactive protein levels [11].…”
Section: Pleiotropic Effects Of Epa In the Atherosclerotic Pathwaymentioning
confidence: 99%
“…EPA also exhibited antioxidant effects in human umbilical vein and glomerular endothelial cells, where it improved the balance between nitric oxide and peroxynitrite [69,70]. These antioxidant effects are thought to be due to intercalation of EPA into the membrane lipid bilayer [68]. …”
Section: Eicosapentaenoic Acid As a Potential Therapeutic Approach Tomentioning
confidence: 99%
“…EPA inhibited lipid peroxidation in membrane vesicles with normal or elevated cholesterol levels as well as glucose-induced pathologic changes in the structural organization of membrane lipids, including development of cholesterol crystalline domains [67,68]. EPA also exhibited antioxidant effects in human umbilical vein and glomerular endothelial cells, where it improved the balance between nitric oxide and peroxynitrite [69,70].…”
Section: Eicosapentaenoic Acid As a Potential Therapeutic Approach Tomentioning
confidence: 99%