Abstract

Saturated fatty acids (SFAs), significant components of both enteral/parenteral nutritional formulations (including diet), are linked to cardiovascular disease complications, such as atherosclerosis. We investigated whether oleic acid (C18:1n-9) reduces the growth inhibitory and pro-inflammatory effects of the stearic acid (C18:0) in human aortic endothelial cells (HAEC). Stearic acid induced growth inhibition at concentrations less than 50 μM, whereas higher concentrations invoked cytotoxicity. Stearic acid-induced growth inhibition and cytotoxic effects were eradicated upon cosupplementation with oleic acid (25 μM). Oleic acid (as low as 5 μM) also inhibited the stearic acid-induced increase in intercellular adhesion molecule-1 (ICAM-1) expression. Stearic acid-induced phosphorylation of nuclear factor-kappa B (NF-κB), a transcriptional regulator of ICAM-1, was also reduced by oleic acid. HAECs supplemented with either stearic or oleic acid resulted in cellular incorporation of C18:0 and C18:1n-9, respectively. Stearic acid primarily incorporated into phospholipids without increasing the total fatty acid content in HAECs. In contrast, oleic acid, with or without stearic acid, incorporated into both phospholipids and triglycerides, with a significant increase in total fatty acid amounts in triglycerides. Our data suggest that oleic acid has the ability to reduce the inflammatory effects of long-chain SFAs in HAECs through reducing cellular stearic acid incorporation and NF-κB activation.

Highlights

  • Saturated fatty acids (SFAs), significant components of both enteral/parenteral nutritional formulations, are linked to cardiovascular disease complications, such as atherosclerosis

  • Saturated fatty acids (SFAs) represent endogenously synthesized and dietary compounds that substantially contribute to the development of coronary artery disease (CAD) [1]

  • We demonstrated that the long-chain saturated fatty acid (SFA) palmitic and stearic acids induce pro-inflammatory responses and initiate the onset of apoptosis in human aortic endothelial cells (HAEC) [17]

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Summary

Introduction

Saturated fatty acids (SFAs), significant components of both enteral/parenteral nutritional formulations (including diet), are linked to cardiovascular disease complications, such as atherosclerosis. We investigated whether oleic acid (C18:1n-9) reduces the growth inhibitory and proinflammatory effects of the stearic acid (C18:0) in human aortic endothelial cells (HAEC). Our data suggest that oleic acid has the ability to reduce the inflammatory effects of long-chain SFAs in HAECs through reducing cellular stearic acid incorporation and NF-␬B activation.—Harvey, K. Oleic acid inhibits stearic acid-induced inhibition of cell growth and pro-inflammatory responses in human aortic endothelial cells. We demonstrated that the long-chain SFAs palmitic and stearic acids induce pro-inflammatory responses and initiate the onset of apoptosis in human aortic endothelial cells (HAEC) [17]. Other investigators have demonstrated that long-chain SFAs, palmitic and stearic acids, induce apoptosis within a variety of vascular cell types [18,19,20,21,22].

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