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首页> 外文期刊>Japanese Journal of Pharmacology >Effect of a Prostaglandin E1 Derivative (OP-1206) and Acetylsalicylic Acid on Electrically Induced Thrombosis in Guinea-Pig Mesenteric Artery and Its Modification by an Inhibitor of Prostaglandin I2 Synthetase, Tranylcypromine
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Effect of a Prostaglandin E1 Derivative (OP-1206) and Acetylsalicylic Acid on Electrically Induced Thrombosis in Guinea-Pig Mesenteric Artery and Its Modification by an Inhibitor of Prostaglandin I2 Synthetase, Tranylcypromine

机译:前列腺素E1衍生物(OP-1206)和乙酰水杨酸对豚鼠肠系膜动脉电致血栓形成的影响及其对前列腺素I2合成酶三苯甲基环丙胺的抑制作用

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References(13) Cited-By(9) The antithrombotic effect of a prostaglandin E1 derivative, OP-1206 (17S-20-dimethyl-trans-Δ2-PGE1)·α-cyclodextrin clathrate (OP-1206·α-CD), was compared with that of acetylsalicylic acid (ASA) in a electrically induced thrombosis model of guinea-pig mesenteric arteries using intact animals and animals subjected to the superfusion of tranylcypromine (TC, 15 mM) over their mesentery. The drug-effect was assessed by the change of the threshold voltage for the thrombus formation. 1) TC (1.5-15 mM) lowered the threshold voltage, and the effect was comparable to its inhibitory effect on PGI2 formation in vitro, suggesting that PGI2 generated in mesenteric arteries acts to prevent thrombus formation. 2) In intact animals, OP-1206·α-CD at doses of 0.01-0.3 mg/kg, p.o. (as OP-1206), significantly and dose-dependently elevated the threshold voltage. ASA (30-1000 mg/kg, p.o.) significantly elevated the threshold voltage, but the effect reached to its maximum at 100 mg/kg and lessened with further increase of ASA. 3) In TC-treated animals, OP-1206·α-CD elevated the threshold voltage dose-dependently, but the elevation of threshold voltage by ASA reached to its plateau level which was significantly lower than that obtained with OP-1206·α-CD at 0.3 mg/kg, indicating that the antithrombotic effect of ASA is incomplete in this model. 4) Threshold voltages in TC-treated animals given OP-1206·α-CD was significantly lower than those in intact animals at all doses tested, but threshold voltages in TC-treated and intact animals given ASA at 300-1000 mg/kg were not different, suggesting that high doses of ASA inhibits PGI2 formation in vivo. Thus, the antithrombotic effect of ASA was restricted by its inhibitory effect on PGI2 formation and its incomplete inhibition on thrombus formation, while such differences were not observed in OP-1206·α-CD.
机译:参考文献(13)(9)引用前列腺素E1衍生物OP-1206(17S-20-二甲基-反-Δ2-PGE1)·α-环糊精包合物(OP-1206·α-CD)的抗血栓形成作用,在完整的动物和在其肠系膜上进行过反式丙氨嘧啶(TC,15 mM)超融合的动物的豚鼠肠系膜动脉电诱发血栓形成模型中,将其与乙酰水杨酸(ASA)进行了比较。通过改变血栓形成的阈值电压来评估药物作用。 1)TC(1.5-15 mM)降低了阈值电压,其效果与其在体外对PGI2形成的抑制作用相当,表明肠系膜动脉中生成的PGI2可以防止血栓形成。 2)在完整的动物中,OP-1206·α-CD的剂量为0.01-0.3 mg / kg,p.o。 (如OP-1206)明显且剂量依赖性地提高了阈值电压。 ASA(30-1000 mg / kg,p.o.)显着提高了阈值电压,但在100 mg / kg时达到了最大值,并随着ASA的进一步增加而减弱。 3)在经过TC处理的动物中,OP-1206·α-CD剂量依赖性地升高阈值电压,但是ASA的阈值电压升高达到其平台水平,这明显低于OP-1206·α-CD获得的阈值水平。 CD为0.3 mg / kg,表明该模型中ASA的抗血栓作用不完全。 4)在所有测试剂量下,给予OP-1206·α-CD的TC处理动物的阈值电压均显着低于完整动物的阈值电压,但给予300-1000 mg / kg的TC处理和完整动物的ASA阈值电压为两者没有什么不同,这表明高剂量的ASA会在体内抑制PGI2的形成。因此,ASA的抗血栓形成作用受其对PGI2形成的抑制作用和对血栓形成的不完全抑制所限制,而在OP-1206·α-CD中未观察到这种差异。

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