Kosugi T, Nakamura M, Saitoh S, Kinjoh K, Hanashiro K
Department of Physiology, School of Medicine, University of the Ryukyus, Okinawa, Japan.
Int J Tissue React. 1992;14(3):141-8.
Ticlopidine hydrochloride and Argipidine were administered simultaneously to rabbits and the changes in platelet function and coagulation-fibrinolysis were determined. Ticlopidine hydrochloride and Argipidine did not give rise to an additive or synergistic effect on the ADP-induced platelet aggregation. However, simultaneous administration of Argipidine and Ticlopidine hydrochloride significantly inhibited the collagen-induced platelet aggregation, as compared to the effect of single administration of Ticlopidine hydrochloride at 60 min after intravenous administration of Argipidine. Furthermore, at 90 min after the intravenous administration, the PAF-induced platelet aggregation in the simultaneous administration was significantly different from that in each individual administration. These results suggested that the effect of simultaneous administration on the platelet aggregation was dependent largely on the effect of Ticlopidine hydrochloride alone.
将盐酸噻氯匹定和阿吉匹定同时给予兔子,并测定血小板功能和凝血纤溶的变化。盐酸噻氯匹定和阿吉匹定对ADP诱导的血小板聚集未产生相加或协同作用。然而,与在静脉注射阿吉匹定60分钟后单独给予盐酸噻氯匹定的效果相比,同时给予阿吉匹定和盐酸噻氯匹定可显著抑制胶原诱导的血小板聚集。此外,在静脉注射后90分钟,同时给药时PAF诱导的血小板聚集与单独给药时显著不同。这些结果表明,同时给药对血小板聚集的作用很大程度上取决于盐酸噻氯匹定单独的作用。