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首页> 外文期刊>Biological research: BR >Inhibitory Effects of Red Wine Extracts on Endothelial-Dependent Adhesive Interactions with Monocytes Induced by Oxysterols
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Inhibitory Effects of Red Wine Extracts on Endothelial-Dependent Adhesive Interactions with Monocytes Induced by Oxysterols

机译:红酒提取物对由胆固醇固醇诱导的内皮依赖性单核细胞黏附相互作用的抑制作用

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摘要

Red wine polyphenolic compounds have been demonstrated to possess antioxidant properties, and several studies have suggested that they might constitute a relevant dietary factor in the protection from coronary heart disease. The aim of the present study is to examine whether red wine extracts (RWE) can ameliorate oxysterol-induced endothelial response, and whether inhibition of adhesion molecule expression is involved in monocyte adhesion to endothelial cells. Surface expression and mRNA levels of adhesion molecules (intercellular adhesion molecule 1 and vascular cell adhesion molecule 1) were determined by ELISA and RT-PCR performed on human aortic endothelial cells (HAEC) monolayers stimulated with 7b-hydroxycholesterol or 25-hydroxycholesterol. Incubation of HAEC with oxysterols (10 muM) increased expression of adhesion molecules in a time-dependent manner. Pretreatment of HAEC with RWE at final concentrations of 1, 10, and 100 ng/ml significantly inhibited the increase of surface protein expression and mRNA levels. Adherence of monocytes to oxysterol-stimulated HAEC was increased compared to that of unstimulated cells. Treatment of HAEC with RWE significantly inhibited adherence of monocytes. These results suggest that RWE works as an anti-atherogenic agent through the inhibition of endothelial-dependent adhesive interactions with monocytes induced by oxysterols
机译:红酒中的多酚化合物已被证明具有抗氧化特性,一些研究表明,它们可能构成预防冠心病的重要饮食因素。本研究的目的是检查红酒提取物(RWE)是否可以改善氧固醇诱导的内皮反应,以及粘附分子表达的抑制作用是否与单核细胞对内皮细胞的粘附有关。通过ELISA和RT-PCR确定粘附分子(细胞间粘附分子1和血管细胞粘附分子1)的表面表达和mRNA水平,所述ELISA和RT-PCR是在用7b-羟基胆固醇或25-羟基胆固醇刺激的人主动脉内皮细胞(HAEC)单层上进行的。 HAEC与氧固醇(10μM)的孵育以时间依赖性方式增加了粘附分子的表达。最终浓度分别为1、10和100 ng / ml的RWE预处理HAEC可以显着抑制表面蛋白表达和mRNA水平的增加。与未经刺激的细胞相比,增加了单核细胞对氧固醇刺激的HAEC的粘附。用RWE治疗HAEC可显着抑制单核细胞的粘附。这些结果表明,RWE通过抑制内皮固醇与氧固醇诱导的单核细胞的黏附相互作用而起到抗动脉粥样硬化作用。

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