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Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity
We tested whether dietary fatty acids alter membrane composition shifting localization of signaling pathways within caveolae to determine their role in vascular function. Wild type (WT) and caveolin‐1‐deficient mice (cav‐1 KO), required for vascular caveolae formation, were fed low fat (LF), high sa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090220/ https://www.ncbi.nlm.nih.gov/pubmed/30105819 http://dx.doi.org/10.14814/phy2.13820 |
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author | Nuno, Daniel W. Coppey, Lawrence J. Yorek, Mark A. Lamping, Kathryn G. |
author_facet | Nuno, Daniel W. Coppey, Lawrence J. Yorek, Mark A. Lamping, Kathryn G. |
author_sort | Nuno, Daniel W. |
collection | PubMed |
description | We tested whether dietary fatty acids alter membrane composition shifting localization of signaling pathways within caveolae to determine their role in vascular function. Wild type (WT) and caveolin‐1‐deficient mice (cav‐1 KO), required for vascular caveolae formation, were fed low fat (LF), high saturated fat (HF, 60% kcal from lard), or high‐fat diet with 50:50 lard and n‐3 polyunsaturated fatty acid‐enriched menhaden oil (MO). HF and MO increased body weight and fat in WT but had less effect in cav‐1 KO. MO increased unsaturated fatty acids and the unsaturation index of aorta from WT and cav‐1 KO. In LF WT aorta, endothelial nitric oxide synthase (eNOS) was localized to cav‐1‐enriched low‐density fractions which shifted to actin‐enriched high‐density fractions with acetylcholine (ACh). HF and MO shifted eNOS to high‐density fractions in WT aorta which was not affected by ACh. In cav‐1 KO aorta, eNOS was localized in low‐density non‐caveolar fractions but not shifted by ACh or diet. Inducible NOS and cyclooxygenase 1/2 were not localized in low‐density fractions or affected by diet, ACh or genotype. ACh‐induced dilation of gracilis arteries from HF WT was similar to dilation in LF but the NOS component was reduced. In WT and cav‐1 KO, dilation to ACh was enhanced by MO through increased role for NOS and cyclooxygenase. We conclude that dietary fats affect vascular fatty acid composition and membrane localization of eNOS but the contribution of eNOS and cyclooxygenase in ACh‐mediated vascular responses is independent of lipid rafts. |
format | Online Article Text |
id | pubmed-6090220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60902202018-08-17 Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity Nuno, Daniel W. Coppey, Lawrence J. Yorek, Mark A. Lamping, Kathryn G. Physiol Rep Original Research We tested whether dietary fatty acids alter membrane composition shifting localization of signaling pathways within caveolae to determine their role in vascular function. Wild type (WT) and caveolin‐1‐deficient mice (cav‐1 KO), required for vascular caveolae formation, were fed low fat (LF), high saturated fat (HF, 60% kcal from lard), or high‐fat diet with 50:50 lard and n‐3 polyunsaturated fatty acid‐enriched menhaden oil (MO). HF and MO increased body weight and fat in WT but had less effect in cav‐1 KO. MO increased unsaturated fatty acids and the unsaturation index of aorta from WT and cav‐1 KO. In LF WT aorta, endothelial nitric oxide synthase (eNOS) was localized to cav‐1‐enriched low‐density fractions which shifted to actin‐enriched high‐density fractions with acetylcholine (ACh). HF and MO shifted eNOS to high‐density fractions in WT aorta which was not affected by ACh. In cav‐1 KO aorta, eNOS was localized in low‐density non‐caveolar fractions but not shifted by ACh or diet. Inducible NOS and cyclooxygenase 1/2 were not localized in low‐density fractions or affected by diet, ACh or genotype. ACh‐induced dilation of gracilis arteries from HF WT was similar to dilation in LF but the NOS component was reduced. In WT and cav‐1 KO, dilation to ACh was enhanced by MO through increased role for NOS and cyclooxygenase. We conclude that dietary fats affect vascular fatty acid composition and membrane localization of eNOS but the contribution of eNOS and cyclooxygenase in ACh‐mediated vascular responses is independent of lipid rafts. John Wiley and Sons Inc. 2018-08-14 /pmc/articles/PMC6090220/ /pubmed/30105819 http://dx.doi.org/10.14814/phy2.13820 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Nuno, Daniel W. Coppey, Lawrence J. Yorek, Mark A. Lamping, Kathryn G. Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity |
title | Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity |
title_full | Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity |
title_fullStr | Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity |
title_full_unstemmed | Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity |
title_short | Dietary fats modify vascular fat composition, eNOS localization within lipid rafts and vascular function in obesity |
title_sort | dietary fats modify vascular fat composition, enos localization within lipid rafts and vascular function in obesity |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090220/ https://www.ncbi.nlm.nih.gov/pubmed/30105819 http://dx.doi.org/10.14814/phy2.13820 |
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