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Novel direct factor IIa and Xa inhibitors: Mechanisms of action and preclinical studies

机译:新型直接因子IIa和Xa抑制剂:作用机理和临床前研究

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The need to overcome certain limitations of the existing anticoagulant agents (heparin, LMWH and VKAs) and to achieve more convenient long-term anticoagulation has fueled the quest for the "ideal anticoagulant", an agent that would exert at least similar antithrombotic effects with a substantially improved pharmacologic profile and significantly less bleeding complications. The major disadvantages of the traditional agents were the narrow therapeutic window with serious drug and food interactions and the need for regular blood monitoring. Coagulation factors IIa and Xa have proved the most attractive pharmacologic targets due to their key role in the coagulation process and the opportunity of blocking thrombin generation before the level of thrombin production that results in amplification of the anticoagulant effect while preserving some of thrombin hemostatic effect. This review summarizes the mechanism of action of some of the most promising novel oral direct factor IIa and Xa inhibitors with a focus on published preclinical trials that led to their clinical development.
机译:克服现有抗凝剂(肝素,LMWH和VKA)的某些局限性以及实现更方便的长期抗凝的需求推动了对“理想的抗凝剂”的追求,“理想的抗凝剂”将发挥至少类似的抗血栓作用并具有抗凝作用。大大改善了药理作用,出血并发症明显减少。传统药物的主要缺点是治疗窗口狭窄,药物和食物之间存在严重的相互作用,并且需要定期进行血液监测。凝血因子IIa和Xa已被证明是最有吸引力的药理学靶标,因为它们在凝血过程中起着关键作用,并在凝血酶产生之前阻止凝血酶生成的机会,从而导致抗凝作用放大,同时保留了某些凝血酶止血作用。这篇综述总结了一些最有前途的新型口服直接因子IIa和Xa抑制剂的作用机理,重点关注导致其临床发展的已发表的临床前试验。

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