Ravn H B, Kristensen S D, Vissinger H, Husted S E
Department of Cardiology, Aarhus University Hospital, Denmark.
Blood Coagul Fibrinolysis. 1996 Mar;7(2):241-4. doi: 10.1097/00001721-199603000-00033.
Magnesium (Mg) may inhibit experimental arterial thrombus formation by inhibition of platelet activity. However, inhibition of platelet aggregation has mainly been shown with high concentrations of magnesium ( > 2 mM). To test the effects of Mg in more clinically relevant concentrations, an in vitro study was performed where platelets were incubated with MgSO4 in the concentration range of 0.5-8.0 mM. Healthy volunteers participated on 2 consecutive days. On Day 2 the volunteers ingested 300 mg of acetylsalicylic acid (ASA) 1 h before blood sampling. Blood was anticoagulated with hirudin and platelet aggregation was performed in platelet-rich plasma (PRP) after incubation with saline or MgSO4 for 5 min. Platelets were stimulated with threshold concentrations of collagen or ADP or a fixed high concentration of collagen (5 micrograms/ml) on both days. A concentration dependent inhibition of platelet aggregation was found after addition of MgSO4. A statistically significant inhibition (P < 0.05) was present at 0.5-1.0 mM MgSO4. The effect of Mg was independent of pretreatment with ASA. Following maximal stimulation with collagen in PRP, a synergistic inhibition of ASA and Mg on platelet aggregation was demonstrated. Administration of MgSO4 in clinically relevant concentrations showed a dose-dependent inhibition of platelet aggregation. Platelet inhibition also occurred after ASA administration and concomitant medication induced a synergistic effect.
镁(Mg)可能通过抑制血小板活性来抑制实验性动脉血栓形成。然而,主要是在高浓度镁(>2 mM)时才显示出对血小板聚集的抑制作用。为了测试更接近临床相关浓度的镁的作用,进行了一项体外研究,将血小板与浓度范围为0.5 - 8.0 mM的硫酸镁孵育。健康志愿者连续两天参与研究。在第2天,志愿者在采血前1小时摄入300毫克乙酰水杨酸(ASA)。血液用水蛭素抗凝,在与生理盐水或硫酸镁孵育5分钟后,在富血小板血浆(PRP)中进行血小板聚集试验。两天均用阈值浓度的胶原或ADP或固定高浓度的胶原(5微克/毫升)刺激血小板。加入硫酸镁后发现血小板聚集呈浓度依赖性抑制。在0.5 - 1.0 mM硫酸镁时存在统计学显著抑制(P < 0.05)。镁的作用与ASA预处理无关。在PRP中用胶原进行最大刺激后,证明了ASA和镁对血小板聚集有协同抑制作用。给予临床相关浓度的硫酸镁显示出对血小板聚集的剂量依赖性抑制。服用ASA后也发生血小板抑制,同时用药可产生协同作用。