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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Lipoic acid, but not tempol, preserves vascular compliance and decreases medial calcification in a model of elastocalcinosis
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Lipoic acid, but not tempol, preserves vascular compliance and decreases medial calcification in a model of elastocalcinosis

机译:在弹性钙化病模型中,硫辛酸(而非tempol)可保持血管顺应性并减少内侧钙化

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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.
机译:血管钙化降低顺应性并增加发病率。该过程的机制尚不清楚。氧化应激的作用和抗氧化剂的作用尚未得到很好的研究。我们调查了抗氧化剂硫辛酸(LA)和tempol在与弹性钙化有关的动脉粥样硬化模型中的作用。每天给雄性新西兰白兔(2.5-3.0 kg)喂普通食物(对照组)或0.5%胆固醇(chol)饮食+104 IU /天的维生素D2(vitD)12周,并接受水处理(车辆, n = 20),0.12 mmol·kg-1·day-1 LA(n = 11)或0.1 mmol·kg-1·day-1 tempol(n = 15)。用Chol + vitD喂养的兔子会形成动脉粥样硬化斑块,与扩张性重构,弹性纤维破裂,内侧钙化和主动脉僵硬相关。从组织学上讲,LA阻止了约60%的内侧钙化和约60%的主动脉硬化。洛杉矶还保留了对收缩剂的反应性,同时内膜中层增厚也有所增加。与LA相反,tempol与斑块胶原蛋白含量增加,内侧钙化和主动脉僵硬相关,并在chol + vitD组中引起血管活性反应的差异性变化。 LA和tempol均可通过chol + vitD阻止超氧化物信号。但是,只有LA通过chol + vitD阻止了过氧化氢相关的信号,而tempol增强了这些信号。这些数据表明,与tempol相反,LA可以通过抑制过氧化氢的产生,最大程度地减少钙化病中钙化和顺应性损失。

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