一种新的苯并咪唑衍生物的抗血小板活性,其结构具有空间上困难的酚代物

A. Spasov, A. Kucheryavenko, K. A. Gaidukova, M. Chernikov, O. Zhukovskaya
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摘要

该研究的目的是研究具有明显抗血小板和抗氧化活性的化合物RU-1144的抗血栓形成特性。采用氯化铁(FeCl3)诱导大鼠颈动脉血栓形成,并与已知抗聚集药物乙酰水杨酸(ASA)、氯吡格雷以及抗氧化剂制剂琥珀酸乙基甲基羟吡啶(EMHPS)进行比较。材料和方法。采用50%三氯化铁(FeCl3)致大鼠颈动脉血栓形成模型和全球血栓形成试验模型(Görög血栓形成试验)研究复方RU-1144的抗血栓活性。这种活性的评估是通过延长血凝块形成的时间来进行的。研究复方RU-1144对小鼠出血时间参数的影响。以乙酰水杨酸、氯吡格雷和EMHPS为对照药物。在氯化铁(FeCl3)致动脉血栓形成模型中,RU-1144物质的抗血栓作用是乙酰水杨酸和氯吡格雷的3.5倍,是EMHPS的2.9倍。在体外全局血栓形成试验(Görög血栓形成试验)模型中,化合物RU-1144与乙酰水杨酸、氯吡格雷具有同等的降低血凝潜能的作用。对RU-1144物质引起的“出血时间”的评估显示,与ASA和氯吡格雷引起的出血延长相比,出血延长的明显程度要低2倍。所进行的研究表明,化合物RU-1144的抗血栓活性明显高于乙酰水杨酸、氯吡格雷和EMHPS,而延长出血时间的能力明显低于参比药物。emhps -琥珀酸乙基甲基羟吡啶;ASA -乙酰水杨酸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ANTITROMBOTIC ACTIVITY OF A NEW BENZIMIDAZOLE DERIVATIVE WITH A SPATIALLY DIFFICULT PHENOLIC SUBSTITUTE IN ITS STRUCTURE
The aim of the study was to investigate antithrombogenic properties of compound RU-1144 with previously identified pronounced antiplatelet and antioxidant activities. The thrombosis induced by Ferric chloride (FeCl3) was carried out in rats’ carotid artery, in comparison with the known antiaggregant drugs - acetylsalicylic acid (ASA) and clopidogrel, as well as with the antioxidant preparation - ethylmethylhydroxypyridine succinate (EMHPS).Materials and methods. The antithrombotic activity of compound RU-1144 was studied on the model of the rats with carotid artery thrombosis, induced by the application of 50% ferric chloride (FeCl3), and the Global Thrombosis Test model (the Görög Thrombosis Test). The evaluation of this type of activity was carried out by prolonging the time of a blood clot formation. The studies of the compound RU-1144 effect on the bleeding time parameter were performed in mice. Acetylsalicylic acid, clopidogrel and EMHPS were used as reference drugs.Results. The antithrombotic effect of the RU-1144 substance revealed in the model of arterial thrombosis induced by the application of ferric chloride (FeCl3), exceeded that of both acetylsalicylic acid and clopidogrel by 3.5 times and that of EMHPS by 2.9 times. In the model of the in vitro Global Thrombosis Test (the Görög Thrombosis Test), compound RU-1144 reduced the thrombogenic potential of the blood equally with acetylsalicylic acid and clopidogrel. The assessment of “the bleeding time”, caused by the RU-1144 substance, showed that the prolongation of bleeding was twice as less pronounced than that caused by ASA and clopidogrel.Conclusion. The performed studies demonstrated a pronounced antithrombotic activity of compound RU-1144, which exceeded that of acetylsalicylic acid, clopidogrel and EMHPS, while the ability to prolong the bleeding time was reliably lower than that of reference drugs.Abbreviations: EMHPS-ethylmethylhydroxypyridine succinate; ASA - acetylsalicylic acid.
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