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1.
Braz J Med Biol Res ; 47(2): 119-27, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24519127

RESUMO

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.


Assuntos
Arteriosclerose/prevenção & controle , Óxidos N-Cíclicos/administração & dosagem , Ácido Tióctico/administração & dosagem , Calcificação Vascular/prevenção & controle , Animais , Aorta Torácica , Arteriosclerose/induzido quimicamente , Arteriosclerose/metabolismo , Complacência (Medida de Distensibilidade)/efeitos dos fármacos , Complacência (Medida de Distensibilidade)/fisiologia , Modelos Animais de Doenças , Masculino , Coelhos , Marcadores de Spin , Calcificação Vascular/induzido quimicamente , Resistência Vascular , Vasoconstrição/efeitos dos fármacos , Vasoconstrição/fisiologia
2.
Braz. j. med. biol. res ; 47(2): 119-127, 2/2014. graf
Artigo em Inglês | LILACS | ID: lil-699771

RESUMO

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.


Assuntos
Animais , Masculino , Coelhos , Arteriosclerose/prevenção & controle , Óxidos N-Cíclicos/administração & dosagem , Ácido Tióctico/administração & dosagem , Calcificação Vascular/prevenção & controle , Aorta Torácica , Arteriosclerose/induzido quimicamente , Arteriosclerose/metabolismo , Complacência (Medida de Distensibilidade)/efeitos dos fármacos , Complacência (Medida de Distensibilidade)/fisiologia , Modelos Animais de Doenças , Marcadores de Spin , Resistência Vascular , Calcificação Vascular/induzido quimicamente , Vasoconstrição/efeitos dos fármacos , Vasoconstrição/fisiologia
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