Bozzo J, Hernández M R, Bastida E, Escolar G, Ordinas A
Servei d'Hemoteràpia i Hemostàsia, Hospital Clínic i Provincial, Barcelona.
Sangre (Barc). 1993 Aug;38(4):273-7.
To assess, by means of a morphometric method, the interaction of platelets with subendothelium, as induced by perfusion with the Baumgartner system, and to compare the antiplatelet effect of acetylsalicylic acid (ASA) and dipyridamole (DIP) and the combination of both drugs.
Blood samples were drawn from healthy volunteers and platelet-rich plasma specimens were prepared at a concentration of 4 x 10(8)/mL. Abdominal aorta segments were obtained from New Zealand rabbits, they being deprived of endothelium by alpha-chymotrypsin. Red cells and platelets were separately or conjointly treated on reconstituted whole blood using ASA and DIP at therapeutic doses, separately or in association. Perfusion experiences were carried out in Baumgartner's annular chamber. Upon finishing the studies, the aorta segments were morphometrically evaluated by an optic analysis system attached to a computer with an automatic image recognition programme. The statistical analysis was performed with Student's t test, differences between groups of p < 0.05 being assigned significance.
Treatment with the association ASA-DIP was the only one to significantly reduce interaction, as both the size of aggregates and the extent of the covered surface decreased when whole blood was treated, and only the covered surface did when red cells were separately treated. When treating only platelets, the reduction of aggregates had no significance.
The synergism of ASA and DIP in antiplatelet therapy was confirmed, as well as the important enhancing effect exerted by red cells.
通过形态计量学方法,评估使用鲍姆加特纳系统灌注诱导血小板与内皮下层的相互作用,并比较乙酰水杨酸(ASA)和双嘧达莫(DIP)以及两种药物联合使用的抗血小板效果。
从健康志愿者采集血样,制备血小板富集血浆标本,浓度为4×10⁸/mL。从新西兰兔获取腹主动脉段,用α-糜蛋白酶去除内皮。使用治疗剂量的ASA和DIP分别或联合对重构全血中的红细胞和血小板进行单独或联合处理。在鲍姆加特纳环形腔室中进行灌注实验。研究结束后,使用连接有自动图像识别程序的计算机的光学分析系统对主动脉段进行形态计量学评估。采用学生t检验进行统计分析,p<0.05的组间差异具有显著性。
仅ASA-DIP联合治疗能显著降低相互作用,在处理全血时聚集物大小和覆盖表面范围均减小,而单独处理红细胞时仅覆盖表面减小。仅处理血小板时,聚集物的减少无显著性。
证实了ASA和DIP在抗血小板治疗中的协同作用,以及红细胞发挥的重要增强作用。