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Time-Dependent Beneficial Effect of Chronic Polyphenol Treatment with Catechin on Endothelial Dysfunction in Aging Mice

机译:儿茶素对慢性多酚的时效性对衰老小鼠血管内皮功能的影响

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摘要

A controlled redox environment is essential for vascular cell maturation and function. During aging, an imbalance occurs, leading to endothelial dysfunction. We hypothesized that, according to the concept of hormesis, exposure to physiologic oxidative stress during the maturation phase of the endothelium will activate protective pathways involved in stress resistance. C57Bl/6 mice were treated with the polyphenol catechin for the last 3 (post-maturation) or 9 months prior study at 12 months of age. Endothelial dysfunction, assessed by acetylcholine-induced dilations of isolated renal arteries, was present at 12 months (P<0.05). Only the 3-month treatment with catechin fully prevented the decline in efficacy and sensitivity to acetylcholine (P<0.05). Splenocytes adhesion to the native endothelium, expression of CD18 and shedding of CD62L and PSGL-1 augmented in 12 months old mice (P<0.05): only 3-month catechin fully normalized adhesion and prevented the expression of adhesion molecules on splenocytes (P<0.05). Aging was associated with vascular gene alterations, which were prevented by 3-month catechin treatment (P<0.05). In contrast, 9-month catechin further increased COX-2, p22phox and reduced MnSOD (P<0.05). In conclusion, we demonstrate a pivotal role of cellular redox equilibrium: exposure to physiologic oxidative stress during the maturation phase of the endothelium is essential for its function.
机译:受控的氧化还原环境对于血管细胞的成熟和功能至关重要。在老化过程中,会发生失衡,从而导致内皮功能障碍。我们假设,根据兴奋剂的概念,在内皮成熟阶段暴露于生理氧化应激会激活参与抗逆性的保护途径。在研究之前的12个月大时,将C57Bl / 6小鼠用多酚儿茶素治疗至少3个月(成熟后)或之前9个月。通过乙酰胆碱诱导的孤立肾动脉扩张评估的内皮功能障碍在12个月时出现(P <0.05)。仅用儿茶素治疗3个月就完全防止了对乙酰胆碱的疗效和敏感性下降(P <0.05)。在12个月大的小鼠中脾细胞对天然内皮的粘附,CD18的表达以及CD62L和PSGL-1的分泌增加(P <0.05):只有3个月的儿茶素使粘附完全标准化,并阻止了脾细胞上粘附分子的表达(P < 0.05)。衰老与血管基因改变有关,而儿茶素治疗3个月可以防止这种情况发生(P <0.05)。相比之下,9个月儿茶素进一步增加COX-2,p22 phox 和降低MnSOD(P <0.05)。总之,我们证明了细胞氧化还原平衡的关键作用:在内皮成熟阶段暴露于生理氧化应激对于其功能至关重要。

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