Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtre
Ajouter des filtres








Gamme d'année
1.
Braz. j. med. biol. res ; 47(2): 119-127, 2/2014. graf
Article Dans Anglais | LILACS | ID: lil-699771

Résumé

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+104 IU/day vitamin D2 (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.


Sujets)
Animaux , Mâle , Lapins , Artériosclérose/prévention et contrôle , N-oxydes cycliques/administration et posologie , Acide lipoïque/administration et posologie , Calcification vasculaire/prévention et contrôle , Aorte thoracique , Artériosclérose/induit chimiquement , Artériosclérose/métabolisme , Compliance/effets des médicaments et des substances chimiques , Compliance/physiologie , Modèles animaux de maladie humaine , Marqueurs de spin , Résistance vasculaire , Calcification vasculaire/induit chimiquement , Vasoconstriction/effets des médicaments et des substances chimiques , Vasoconstriction/physiologie
2.
Arq. bras. cardiol ; 101(6,supl.2): 1-63, 2013. tab, graf
Article Dans Portugais | LILACS | ID: lil-702008
SÉLECTION CITATIONS
Détails de la recherche