Sinzinger H
Wilhelm Auerswald-Atheroskleroseforschungsgruppe (ASF) Wien, Osterreich.
Z Kardiol. 1991;80 Suppl 5:51-3.
In order to test the hypothesis, whether molsidomine acts as an in-vivo NO-donor, we examined the synergism of PGI2 and molsidomine in patients with peripheral vascular disease. The effect was quantified by measuring the platelet uptake at atherosclerotic lesion sites, as well as measuring the platelet survival after radiolabelling the autologous platelets with 111Indium-oxine. The combination of both substances achieved a significantly higher (p less than 0.01) benefit in comparison to single administration of either of the components. This synergism was shown via a decrease in thrombogenicity and a prolongation in platelet survival. These data indicate that a potentiating synergism of hemostatic regulation can be achieved via an in-vivo interaction between NO and PGI2.
为了验证吗多明是否作为体内一氧化氮供体这一假设,我们研究了前列环素(PGI2)与吗多明在周围血管疾病患者中的协同作用。通过测量动脉粥样硬化病变部位的血小板摄取量以及用111铟 - 氧嗪对自体血小板进行放射性标记后测量血小板存活率来量化该效应。与单独使用任何一种成分相比,两种物质联合使用产生了显著更高(p小于0.01)的益处。这种协同作用通过血栓形成性降低和血小板存活时间延长得以体现。这些数据表明,通过一氧化氮与前列环素在体内的相互作用,可以实现止血调节的增强协同作用。