Christensen Kjeld, Larsson Rolf, Emanuelsson Håkan, Elgue Graciela, Larsson Anders
Division of Cardiology, University Hospital, Orebro, Sweden.
Platelets. 2006 Aug;17(5):318-27. doi: 10.1080/09537100600746557.
The effect of the direct platelet P2Y12 receptor inhibitor, AR-C69931MX, on activation of blood induced by stents with and without heparin coating was investigated using a whole blood Chandler loop model in vitro. Stents were deployed in Chandler loops. Fresh human blood with heparin and AR-C69931MX was rotated for 1 h at 37 degrees C and used for measurements of platelets, microparticles, thrombin-antithrombin complex (TAT), fibrinogen binding to platelets, P-selectin expression by platelets, CD11b, Prothrombin Fragment F1+2, FXIa-AT, FXIIa-AT, C3a, sC5b-9 and stent score. In the first experiment there were four study groups with unmodified stents: 1a, no AR-C69931MX; 1b, 250 nmol/L; 1c, 750 nmol/L; 1d, 2250 nmol/L of AR-C69931MX. In the second experiment the concentration of AR-C69931MX was 500 nmol/L: 2a; tubings without stent; 2b; tubings with heparin-coated stent; 2c; tubings with unmodified stents. Heparin-coated stents were used in the third experiment: 3a; no AR-C69931MX; 3b; 500 nmol/L of AR-C69931MX. In the first experiment there were significant differences in all parameters analysed except for C3a, and stent score when the group with no AR-C69931MX was compared to all the groups with AR-C69931MX. In the second experiment there were significant differences in platelet count, TAT, FXIa-AT, FXIIa-AT and stent score when unmodified stents were compared to loops with no stents and partly to loops with heparin-coated stents. In the third experiment there was a significant reduction in generation of TAT, stent score and better preservation of platelet number by combining the platelet inhibitor and heparin-coated stents as compared to heparin-coated stents alone. The conclusion is that the direct P2Y12 receptor inhibitor AR-C69931MX reduced the different aspects of activation of blood induced by both unmodified and heparin-coated stents.
使用全血钱德勒环路模型在体外研究了直接血小板P2Y12受体抑制剂AR-C69931MX对有肝素涂层和无肝素涂层支架诱导的血液激活的影响。将支架放置在钱德勒环路中。含有肝素和AR-C69931MX的新鲜人血在37℃下旋转1小时,用于测量血小板、微粒、凝血酶-抗凝血酶复合物(TAT)、纤维蛋白原与血小板的结合、血小板P-选择素表达、CD11b、凝血酶原片段F1+2、FXIa-AT、FXIIa-AT、C3a、sC5b-9和支架评分。在第一个实验中,有四个使用未修饰支架的研究组:1a,无AR-C69931MX;1b,250 nmol/L;1c,750 nmol/L;1d,2250 nmol/L的AR-C69931MX。在第二个实验中,AR-C69931MX的浓度为500 nmol/L:2a,无支架的管路;2b,有肝素涂层支架的管路;2c,有未修饰支架的管路。在第三个实验中使用了肝素涂层支架:3a,无AR-C69931MX;3b,500 nmol/L的AR-C69931MX。在第一个实验中,当将无AR-C69931MX的组与所有含AR-C69931MX的组进行比较时,除C3a和支架评分外,所有分析参数均存在显著差异。在第二个实验中,当将未修饰支架与无支架的环路以及部分与有肝素涂层支架的环路进行比较时,血小板计数、TAT、FXIa-AT、FXIIa-AT和支架评分存在显著差异。在第三个实验中,与单独使用肝素涂层支架相比,联合使用血小板抑制剂和肝素涂层支架可使TAT生成显著减少、支架评分降低且血小板数量得到更好的保存。结论是直接P2Y12受体抑制剂AR-C69931MX减少了未修饰和肝素涂层支架诱导的血液激活的不同方面。