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首页> 外文期刊>Cardiovascular therapeutics >Ascorbic acid infusion blunts CD40L upregulation in patients undergoing coronary stent.
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Ascorbic acid infusion blunts CD40L upregulation in patients undergoing coronary stent.

机译:抗坏血酸输注能使接受冠状动脉支架治疗的患者的CD40L上调。

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OBJECTIVES: To reduce the increase of oxidative stress and the upregulation of CD40L during stenting procedure using ascorbic acid infusion. Background: CD40L upregulation occurring after coronary Percutaneous Coronary Intervention predicts vascular events but the underlying mechanism is still unclear. METHODS: Fifty-six patients undergoing elective coronary stenting were randomly allocated to intravenous infusion of the antioxidant ascorbic acid or placebo. Platelet CD40L and plasma levels of soluble CD40L and of 8-hydroxy-2'-deoxyguanosine, a marker of oxidative stress, were measured before and after coronary stenting. In vitro study was also done to measure reactive oxidant species and CD40L expression in platelets exposed to anoxia-reoxygenation. RESULTS: Placebo-treated patients showed a significant increase of platelet CD40L, soluble CD40L and 8-hydroxy-2'-deoxyguanosine compared to baseline values. Patients given ascorbic acid showed no change of soluble CD40L and platelet CD40L but a significant decrease of 8-hydroxy-2'-deoxyguanosine. After 60 and 120 min, soluble CD40L, platelet CD40L and 8-hydroxy-2'-deoxyguanosine were significantly lower in the ascorbic acid-treated group compared to the placebo-treated one. A significant correlation between platelet CD40L and soluble CD40L and between soluble CD40L and 8-hydroxy-2'-deoxyguanosine was observed. Platelets, in vitro exposed to anoxia-reoxygenation, had a burst of ROS and an upregulation of CD40L that were inhibited by ascorbic acid or apocynin, an inhibitor of NADPH oxidase. CONCLUSIONS: This study shows that in patients undergoing coronary stenting CD40L is upregulated with a mechanism which is likely mediated by oxidative stress.
机译:目的:在抗坏血酸输注支架置入过程中,减少氧化应激的增加和CD40L的上调。背景:冠状动脉经皮冠状动脉介入治疗后发生CD40L上调可预测血管事件,但其潜在机制仍不清楚。方法:将56例行择期冠状动脉支架置入术的患者随机分配为抗氧化剂抗坏血酸或安慰剂静脉输注。在冠状动脉支架置入术之前和之后,测量血小板CD40L和血浆中可溶性CD40L以及8-羟基-2'-脱氧鸟苷的血浆水平(氧化应激的标志)。还进行了体外研究,以测定暴露于缺氧-再氧化的血小板中的反应性氧化剂和CD40L表达。结果:与基线值相比,安慰剂治疗的患者显示血小板CD40L,可溶性CD40L和8-羟基-2'-脱氧鸟苷显着增加。接受抗坏血酸治疗的患者的可溶性CD40L和血小板CD40L没有变化,但是8-hydroxy-2'-deoxyguanosine明显下降。在60和120分钟后,抗坏血酸治疗组的可溶性CD40L,血小板CD40L和8-羟基-2'-脱氧鸟苷的水平明显低于安慰剂治疗组。观察到血小板CD40L和可溶性CD40L之间以及可溶性CD40L和8-羟基-2'-脱氧鸟苷之间的显着相关性。体外暴露于缺氧-复氧的血小板中,抗坏血酸或载脂蛋白(NADPH氧化酶的抑制剂)抑制了ROS的爆发和CD40L的上调。结论:这项研究表明,在接受冠状动脉支架置入术的患者中,CD40L的表达可能由氧化应激介导。

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