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首页> 外文期刊>BMJ Open >Effect of ω-3 fatty acid supplementation on endothelial function, endogenous fibrinolysis and platelet activation in patients with a previous myocardial infarction: a randomised controlled trial
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Effect of ω-3 fatty acid supplementation on endothelial function, endogenous fibrinolysis and platelet activation in patients with a previous myocardial infarction: a randomised controlled trial

机译:补充ω-3脂肪酸对既往心肌梗死患者内皮功能,内源性纤溶和血小板活化的影响:一项随机对照试验

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摘要

Objective The mechanisms through which ω-3 fatty acids reduce adverse cardiac events remain uncertain. We aimed to investigate the effect of ω-3 fatty acid supplementation on endothelial vasomotor function, endogenous fibrinolysis, and platelet and monocyte activation in patients with coronary heart disease. Design Randomised, double-blind, placebo-controlled, cross-over trial. Setting Academic cardiac centre. Participants 20 male patients with a previous myocardial infarction. Intervention ω-3 Fatty acid supplementation (2?g/day for 6?weeks) versus olive oil placebo. Outcome measures Peripheral blood was taken for analysis of platelet and monocyte activation, and forearm blood flow (FBF) was assessed in a subset of 12 patients during intrabrachial infusions of acetylcholine, substance P and sodium nitroprusside. Stimulated plasma tissue plasminogen activator (t-PA) concentrations were measured during substance P infusion. Results All vasodilators caused dose-dependent increases in FBF (p0.0001). ω-3 Fatty acid supplementation did not affect endothelium-dependent vasodilation with acetylcholine and substance P compared with placebo (p=0.5 and 0.9). Substance P caused a dose-dependent increase in plasma t-PA concentrations (p0.0001), which was not affected by ω-3 fatty acid supplementation (p=0.9). ω-3 Fatty acids did not affect platelet–monocyte aggregation, platelet P-selectin or CD40L, or monocyte CD40. Conclusions We have demonstrated that dietary supplementation with ω-3 fatty acids does not affect endothelial vasomotor function, endothelial t-PA release, or platelet and monocyte activation in patients with coronary heart disease. Cardiac benefits conferred by ω-3 fatty acids in coronary heart disease are unlikely to be mediated through effects on these systems.
机译:目的ω-3脂肪酸减少不良心脏事件的机制尚不清楚。我们旨在研究补充ω-3脂肪酸对冠心病患者内皮血管舒缩功能,内源性纤维蛋白溶解以及血小板和单核细胞活化的影响。设计随机,双盲,安慰剂对照,交叉试验。设置学术心脏中心。参加者20例先前有心肌梗塞的男性患者。干预ω-3与橄榄油安慰剂相比,补充脂肪酸(每天2微克/天,共6周)。结果措施抽取外周血用于分析血小板和单核细胞的活化,并在臂内输注乙酰胆碱,P物质和硝普钠的12名患者中评估前臂血流量(FBF)。在P物质输注过程中测量了刺激的血浆组织纤溶酶原激活物(t-PA)浓度。结果所有血管扩张剂均导致FBF剂量依赖性增加(p <0.0001)。与安慰剂相比,ω-3脂肪酸补充剂对乙酰胆碱和P物质的内皮依赖性血管舒张作用没有影响(p = 0.5和0.9)。 P物质导致血浆t-PA浓度呈剂量依赖性增加(p <0.0001),不受ω-3脂肪酸补充的影响(p = 0.9)。 ω-3脂肪酸不影响血小板-单核细胞聚集,血小板P-选择素或CD40L或单核细胞CD40。结论我们已经证明,饮食中添加ω-3脂肪酸不会影响冠心病患者的血管内皮功能,内皮t-PA释放或血小板和单核细胞活化。 ω-3脂肪酸赋予冠心病的心脏益处不太可能通过对这些系统的作用来介导。

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