Imura Y, Terashita Z, Shibouta Y, Nishikawa K
Biology Laboratories, Takeda Chemical Industries, Ltd., Osaka, Japan.
Eur J Pharmacol. 1988 Mar 15;147(3):359-65. doi: 10.1016/0014-2999(88)90169-0.
The thromboxane A2/prostaglandin endoperoxide (TXA2/PGH2) receptor antagonist activity of CV-4151, a potent TXA2 synthetase inhibitor, was examined. CV-4151 inhibited guinea pig and human platelet aggregation induced by U-44069 with IC50 values of 1.2 +/- 0.3 X 10(-5) and 1.9 +/- 0.4 X 10(-5) M, respectively, and inhibited the specific binding of [3H]U-46619 to washed guinea pig and human platelets with IC50 values of 1.2 +/- 0.3 X 10(-6) and 5.1 +/- 1.0 X 10(-6) M, respectively. CV-4151 competitively inhibited the contraction of rabbit aortic strips induced by U-44069 with a pA2 value of 5.90. In experiments in mice in vivo, CV-4151 (1 and 10 mg/kg i.v.) significantly inhibited the thrombocytopenia induced by U-44069 in a dose-dependent manner. These results show that CV-4151 has a distinct TXA2/PGH2 receptor antagonist effect, and that this effect together with its inhibition of TXA2 synthetase could be important for the pharmacological action of this compound.
对强效血栓素A2合成酶抑制剂CV - 4151的血栓素A2/前列腺素内过氧化物(TXA2/PGH2)受体拮抗活性进行了研究。CV - 4151抑制U - 44069诱导的豚鼠和人血小板聚集,其IC50值分别为1.2±0.3×10⁻⁵和1.9±0.4×10⁻⁵ M,并且抑制[³H]U - 46619与洗涤过的豚鼠和人血小板的特异性结合,IC50值分别为1.2±0.3×10⁻⁶和5.1±1.0×10⁻⁶ M。CV - 4151竞争性抑制U - 44069诱导的兔主动脉条收缩,pA2值为5.90。在小鼠体内实验中,CV - 4151(静脉注射1和10 mg/kg)以剂量依赖方式显著抑制U - 44069诱导的血小板减少。这些结果表明CV - 4151具有明显的TXA2/PGH2受体拮抗作用,并且这种作用与其对TXA2合成酶的抑制作用一起可能对该化合物的药理作用很重要。