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金精三羧酸对大鼠和豚鼠动脉血栓形成的抗血栓作用的比较研究。

A comparative study of the antithrombotic effect of aurintricarboxylic acid on arterial thrombosis in rats and guinea pigs.

作者信息

Takiguchi Y, Shimazawa M, Nakashima M

机构信息

Department of Pharmacology, Hamamatsu University School of Medicine, Japan.

出版信息

Br J Pharmacol. 1996 Aug;118(7):1633-8. doi: 10.1111/j.1476-5381.1996.tb15585.x.

Abstract
  1. The antithrombotic effect of aurintricarboxylic acid (ATA) which inhibits binding of von Willebrand factor (vWF) to platelet glycoprotein lb (GPlb) receptor was evaluated in photochemically-induced thrombosis models in the femoral artery of rats and guinea-pigs. 2. ATA at a dose of 10 mg kg-1 significantly prolonged the time required for thrombotic occlusion of the artery in rats. The antithrombotic efficacy was associated with a significant inhibition of platelet retention and ex vivo botrocetin-induced platelet aggregation. 3. On the other hand, in guinea-pigs, ATA at the same dose inhibited the platelet retention and the platelet aggregation, but did not prevent thromboocclusion. 4. ATA inhibited aggregation of washed platelets from rats or guinea-pigs in response to botrocetin and thrombin in a dose-dependent manner (1-30 microM), and to the same extent. 5. ATA moderately increased activated partial thromboplastin time and bleeding time in both species. 6. These results indicate that vWF may play a role in the development of occlusive arterial thrombosis in the rat, but not in the guinea-pig. 7. The antithrombotic activity of ATA may partly arise from its inhibitory effect on thrombin, in addition to that on the vWF-GPlb pathway
摘要
  1. 在大鼠和豚鼠股动脉的光化学诱导血栓形成模型中,评估了金精三羧酸(ATA)抑制血管性血友病因子(vWF)与血小板糖蛋白lb(GPlb)受体结合的抗血栓作用。2. 剂量为10 mg kg-1的ATA显著延长了大鼠动脉血栓闭塞所需的时间。抗血栓疗效与血小板滞留的显著抑制和体外蛇毒诱导的血小板聚集有关。3. 另一方面,在豚鼠中,相同剂量的ATA抑制了血小板滞留和血小板聚集,但并未防止血栓闭塞。4. ATA以剂量依赖方式(1-30 microM)抑制来自大鼠或豚鼠的洗涤血小板对蛇毒和凝血酶的聚集,且抑制程度相同。5. ATA适度增加了两个物种的活化部分凝血活酶时间和出血时间。6. 这些结果表明,vWF可能在大鼠闭塞性动脉血栓形成的发展中起作用,但在豚鼠中不起作用。7. ATA的抗血栓活性可能部分源于其对凝血酶的抑制作用,此外还源于对vWF-GPlb途径的抑制作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0892/1909856/768a82a16915/brjpharm00086-0080-a.jpg

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