Inoue K, Aoki Y, Hayashi M, Kitahara S, Tanabe H, Kiyoki M, Araki H
Pharmacological Research Department, Teijin Institute for Bio-medical Research, Teijin Ltd., Toyko, Japan.
Arzneimittelforschung. 1995 Sep;45(9):980-4.
Effect of TTC-909, a chemically stable isocarbacyclin methyl ester (CAS 88931-51-5, TEI-9090) incorporated in lipid microspheres, on platelet aggregation was tested in conscious rabbits. TTC-909 significantly inhibited platelet aggregation induced by ADP at early times after bolus i.v. injection from the dose of 0.3 micrograms/kg in a dose-dependent manner. Similarly, TTC-909 significantly inhibited platelet aggregation induced by ADP during the venous infusion from the dose of 100 ng/kg/min, also in a dose-dependent manner. The anti-platelet effect of TTC-909 was observed at a dose lower than that inducing hypotensive effect when given as both bolus i.v. and venous infusion. On the other hand, prostaglandin (PG) E1 (LM)--PGE1 incorporated in lipid microspheres--reduced blood pressure without having an anti-platelet effect. These results indicate that TTC-909 may be a potent anti-thrombotic drug.
测试了脂质微球包裹的化学稳定的异前列环素甲酯(TTC - 909,CAS 88931 - 51 - 5,TEI - 9090)对清醒家兔血小板聚集的影响。静脉推注后早期,TTC - 909以剂量依赖性方式从0.3微克/千克的剂量开始显著抑制由ADP诱导的血小板聚集。同样,静脉输注期间,TTC - 909从100纳克/千克/分钟的剂量开始也以剂量依赖性方式显著抑制由ADP诱导的血小板聚集。当以静脉推注和静脉输注方式给药时,观察到TTC - 909产生抗血小板作用的剂量低于引起降压作用的剂量。另一方面,脂质微球包裹的前列腺素(PG)E1(PGE1 - LM)可降低血压,但没有抗血小板作用。这些结果表明,TTC - 909可能是一种有效的抗血栓药物。