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Lipoic acid, but not tempol, preserves vascular compliance and decreases medial calcification in a model of elastocalcinosis
Vascular calcification decreases compliance and increases morbidity. Mechanisms of this process are unclear. The role of oxidative stress and effects of antioxidants have been poorly explored. We investigated effects of the antioxidants lipoic acid (LA) and tempol in a model of atherosclerosis assoc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051185/ https://www.ncbi.nlm.nih.gov/pubmed/24519127 http://dx.doi.org/10.1590/1414-431X20133193 |
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author | Bassi, E. Liberman, M. Martinatti, M.K. Bortolotto, L.A. Laurindo, F.R.M. |
author_facet | Bassi, E. Liberman, M. Martinatti, M.K. Bortolotto, L.A. Laurindo, F.R.M. |
author_sort | Bassi, E. |
collection | PubMed |
description | Vascular calcification decreases compliance and increases morbidity. Mechanisms of this process are unclear. The role of oxidative stress and effects of antioxidants have been poorly explored. We investigated effects of the antioxidants lipoic acid (LA) and tempol in a model of atherosclerosis associated with elastocalcinosis. Male New Zealand white rabbits (2.5-3.0 kg) were fed regular chow (controls) or a 0.5% cholesterol (chol) diet+10(4) IU/day vitamin D(2) (vitD) for 12 weeks, and assigned to treatment with water (vehicle, n=20), 0.12 mmol·kg(-1)·day(-1) LA (n=11) or 0.1 mmol·kg(-1)·day(-1) tempol (n=15). Chol+vitD-fed rabbits developed atherosclerotic plaques associated with expansive remodeling, elastic fiber disruption, medial calcification, and increased aortic stiffness. Histologically, LA prevented medial calcification by ∼60% and aortic stiffening by ∼60%. LA also preserved responsiveness to constrictor agents, while intima-media thickening was increased. In contrast to LA, tempol was associated with increased plaque collagen content, medial calcification and aortic stiffness, and produced differential changes in vasoactive responses in the chol+vitD group. Both LA and tempol prevented superoxide signals with chol+vitD. However, only LA prevented hydrogen peroxide-related signals with chol+vitD, while tempol enhanced them. These data suggest that LA, opposite to tempol, can minimize calcification and compliance loss in elastocalcionosis by inhibition of hydrogen peroxide generation. |
format | Online Article Text |
id | pubmed-4051185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-40511852014-06-10 Lipoic acid, but not tempol, preserves vascular compliance and decreases medial calcification in a model of elastocalcinosis Bassi, E. Liberman, M. Martinatti, M.K. Bortolotto, L.A. Laurindo, F.R.M. Braz J Med Biol Res Biomedical Sciences Vascular calcification decreases compliance and increases morbidity. Mechanisms of this process are unclear. The role of oxidative stress and effects of antioxidants have been poorly explored. We investigated effects of the antioxidants lipoic acid (LA) and tempol in a model of atherosclerosis associated with elastocalcinosis. Male New Zealand white rabbits (2.5-3.0 kg) were fed regular chow (controls) or a 0.5% cholesterol (chol) diet+10(4) IU/day vitamin D(2) (vitD) for 12 weeks, and assigned to treatment with water (vehicle, n=20), 0.12 mmol·kg(-1)·day(-1) LA (n=11) or 0.1 mmol·kg(-1)·day(-1) tempol (n=15). Chol+vitD-fed rabbits developed atherosclerotic plaques associated with expansive remodeling, elastic fiber disruption, medial calcification, and increased aortic stiffness. Histologically, LA prevented medial calcification by ∼60% and aortic stiffening by ∼60%. LA also preserved responsiveness to constrictor agents, while intima-media thickening was increased. In contrast to LA, tempol was associated with increased plaque collagen content, medial calcification and aortic stiffness, and produced differential changes in vasoactive responses in the chol+vitD group. Both LA and tempol prevented superoxide signals with chol+vitD. However, only LA prevented hydrogen peroxide-related signals with chol+vitD, while tempol enhanced them. These data suggest that LA, opposite to tempol, can minimize calcification and compliance loss in elastocalcionosis by inhibition of hydrogen peroxide generation. Associação Brasileira de Divulgação Científica 2014-02-17 /pmc/articles/PMC4051185/ /pubmed/24519127 http://dx.doi.org/10.1590/1414-431X20133193 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedical Sciences Bassi, E. Liberman, M. Martinatti, M.K. Bortolotto, L.A. Laurindo, F.R.M. Lipoic acid, but not tempol, preserves vascular compliance and decreases medial calcification in a model of elastocalcinosis |
title | Lipoic acid, but not tempol, preserves vascular
compliance and decreases medial calcification in a model of
elastocalcinosis |
title_full | Lipoic acid, but not tempol, preserves vascular
compliance and decreases medial calcification in a model of
elastocalcinosis |
title_fullStr | Lipoic acid, but not tempol, preserves vascular
compliance and decreases medial calcification in a model of
elastocalcinosis |
title_full_unstemmed | Lipoic acid, but not tempol, preserves vascular
compliance and decreases medial calcification in a model of
elastocalcinosis |
title_short | Lipoic acid, but not tempol, preserves vascular
compliance and decreases medial calcification in a model of
elastocalcinosis |
title_sort | lipoic acid, but not tempol, preserves vascular
compliance and decreases medial calcification in a model of
elastocalcinosis |
topic | Biomedical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051185/ https://www.ncbi.nlm.nih.gov/pubmed/24519127 http://dx.doi.org/10.1590/1414-431X20133193 |
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