Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.

Factors implicated in the development of atherosclerosis include metabolic alterations of the endothelium induced by certain lipids and inflammatory cytokines. To study the hypothesis that the combined presence of unsaturated fatty acids and inflammatory cytokines may cross-amplify their individual...

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Main Authors: M Toborek, S W Barger, M P Mattson, S Barve, C J McClain, B Hennig
Format: Article
Language:English
Published: Elsevier 1996-01-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520376410
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author M Toborek
S W Barger
M P Mattson
S Barve
C J McClain
B Hennig
author_facet M Toborek
S W Barger
M P Mattson
S Barve
C J McClain
B Hennig
author_sort M Toborek
collection DOAJ
description Factors implicated in the development of atherosclerosis include metabolic alterations of the endothelium induced by certain lipids and inflammatory cytokines. To study the hypothesis that the combined presence of unsaturated fatty acids and inflammatory cytokines may cross-amplify their individual injurious effects, cultured endothelial cells were treated with 90 mu M of linoleic acid (18:2 n-6) and/or 20 ng/ml (100 U/ml) of tumor necrosis factor-alpha (TNF) for up to 24 h. Disturbances in endothelial cell metabolism were determined by measuring cellular oxidative stress, oxidative stress-inducible nuclear factor-kappa B (NF-kappa B) and NF-kappa B-related transcription, intracellular calcium levels, and endothelial barrier function reflected by transendothelial albumin movement. Both 18:2 and TNF increased cellular oxidation, intracellular calcium, and endothelial barrier permeability. These changes were cross-amplified in cells treated both with 18:2 and TNF, compared with 18:2 or TNF alone. In contrast, a combined exposure to 18:2 and TNF did not potentiate effects mediated by 18:2 or TNF alone on NF-kappa B activation or NF-kappa B-related transcription. Pretreatment with 25 mu M vitamin E attenuated 18:2 and/or TNF-mediated endothelial cell dysfunction. These results suggest that certain unsaturated fatty acids can potentiate TNF-mediated endothelial cell dysfunction and that oxidative stress may be partially responsible for these metabolic events. These findings have implications for understanding lipid-mediated inflammatory responses in atherosclerosis.
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spelling doaj.art-98cfb874d1614174a2ffd86b455ac6bb2022-12-21T19:36:36ZengElsevierJournal of Lipid Research0022-22751996-01-01371123135Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.M Toborek0S W Barger1M P Mattson2S Barve3C J McClain4B Hennig5Departments of Nutrition and Food Science, University of Kentucky, Lexington 40506-0054, USA.Departments of Nutrition and Food Science, University of Kentucky, Lexington 40506-0054, USA.Departments of Nutrition and Food Science, University of Kentucky, Lexington 40506-0054, USA.Departments of Nutrition and Food Science, University of Kentucky, Lexington 40506-0054, USA.Departments of Nutrition and Food Science, University of Kentucky, Lexington 40506-0054, USA.Departments of Nutrition and Food Science, University of Kentucky, Lexington 40506-0054, USA.Factors implicated in the development of atherosclerosis include metabolic alterations of the endothelium induced by certain lipids and inflammatory cytokines. To study the hypothesis that the combined presence of unsaturated fatty acids and inflammatory cytokines may cross-amplify their individual injurious effects, cultured endothelial cells were treated with 90 mu M of linoleic acid (18:2 n-6) and/or 20 ng/ml (100 U/ml) of tumor necrosis factor-alpha (TNF) for up to 24 h. Disturbances in endothelial cell metabolism were determined by measuring cellular oxidative stress, oxidative stress-inducible nuclear factor-kappa B (NF-kappa B) and NF-kappa B-related transcription, intracellular calcium levels, and endothelial barrier function reflected by transendothelial albumin movement. Both 18:2 and TNF increased cellular oxidation, intracellular calcium, and endothelial barrier permeability. These changes were cross-amplified in cells treated both with 18:2 and TNF, compared with 18:2 or TNF alone. In contrast, a combined exposure to 18:2 and TNF did not potentiate effects mediated by 18:2 or TNF alone on NF-kappa B activation or NF-kappa B-related transcription. Pretreatment with 25 mu M vitamin E attenuated 18:2 and/or TNF-mediated endothelial cell dysfunction. These results suggest that certain unsaturated fatty acids can potentiate TNF-mediated endothelial cell dysfunction and that oxidative stress may be partially responsible for these metabolic events. These findings have implications for understanding lipid-mediated inflammatory responses in atherosclerosis.http://www.sciencedirect.com/science/article/pii/S0022227520376410
spellingShingle M Toborek
S W Barger
M P Mattson
S Barve
C J McClain
B Hennig
Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.
Journal of Lipid Research
title Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.
title_full Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.
title_fullStr Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.
title_full_unstemmed Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.
title_short Linoleic acid and TNF-alpha cross-amplify oxidative injury and dysfunction of endothelial cells.
title_sort linoleic acid and tnf alpha cross amplify oxidative injury and dysfunction of endothelial cells
url http://www.sciencedirect.com/science/article/pii/S0022227520376410
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