外源性纤维蛋白单体在摄入华法林的创伤后出血模型中的形态学、止血学和止血学研究

V. M. Vdovin, I. Shakhmatov, I. Bobrov, D. Orekhov, Vyacheslav V. Teryayev, V. E. Chernus', A. Momot
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引用次数: 0

摘要

简介:早些时候,我们在华法林凝血病的实验模型上建立了外源性纤维蛋白单体(FM)在低剂量下显著限制创伤后失血的能力。然而,没有考虑到伤口区域纤维蛋白形成的形态学特征。目的:比较外源性FM系统应用的形态学、止血学和止血学数据,以解释其在华法林基础摄入的创伤后出血模型中的作用。材料与方法:选用栗鼠公兔。在动物摄入华法林(0.0.4 mg/kg/d / s,持续2周)的基础上,初步系统引入FM(静脉注射0.25 mg/kg)或凝血酶原复合物因子浓缩物(静脉注射40 IU/kg),对创伤后伤口区域的止血效果和肝脏表面的形态学图像进行了比较分析。结果:在华法林化动物中,在实验性肝损伤的条件下,引入FM促进了与凝血酶原复合因子浓缩物相当的止血效果。两种止血药物都能导致纤维蛋白的强烈形成,从而减少创伤后失血。与安慰剂相比,使用FM与伤口表面血栓沉积和纤维蛋白纤维的厚度分别增加4.0倍和1.6倍相关(0.000001)。这一过程积极涉及血小板,导致伤口附近血管腔内血小板数量减少1.7倍(0.0002)。与凝血酶原复合因子的浓度相比,FM对静脉血的全身止血反应没有影响。结论:外源性FM对实验性大剂量外伤和摄入华法林引起的凝血功能障碍具有局部止血作用。止血作用是通过创面强烈的血栓形成和血小板的积极募集来介导的。虽然尚未确定FM的作用机制,但其已证明的效果的特殊性可能是介导的,这需要在该方向上继续研究。
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Morphologic, Hemostasiologic and Hemostatic Aspects of Systemic Application of Exogenous Fibrin Monomer in Model of Posttraumatic Bleeding with Underlying Intake of Warfarin
INTRODUCTION: Earlier, an ability of exogenous fibrin monomer (FM) introduced at low doses to considerably limit posttraumatic blood loss was established by us on an experimental model of warfarin coagulopathy in vivo. However, the morphologic peculiarities of fibrin formation in the wound area were not considered. AIM: To compare morphologic, hemostasiologic and hemostatic data based on the results of systemic application of exogenous FM to interpret their effects in the model of posttraumatic bleeding with the underlying intake of warfarin. MATERIALS AND METHODS: In the work, Chinchilla male rabbits were used. A comparative analysis of hemostasiologic effects and of morphologic picture of the surface of the liver in the wound area was conducted after a dosed trauma, with a preliminary systemic introduction of FM (0.25 mg/kg intravenously) or a concentrate of prothrombin complex factors (40 IU/kg intravenously) with the underlying intake of warfarin by animals (0.40.5 mg/kg/day per os for 2 weeks). RESULTS: Introduction of FM in warfarinised animals in the conditions of a dosed experimental liver injury promoted a hemostatic effect comparable with that of a concentrate of prothrombin complex factors. Both hemostatic drugs led to intense fibrin formation that reduced posttraumatic blood loss. The use of FM was associated with increase in the thickness of thrombotic deposits and fibrin fibers in the wound surface in comparison with placebo by 4.0 and 1.6 times, respectively (р 0.000001). This process actively involved platelets, which led to 1.7 times reduction of their quantity in the lumen of the blood vessels in the wound vicinity (р 0.0002). No effect of FM on systemic hemostatic reactions in venous blood was found, in contrast to concentrate of prothrombin complex factors. CONCLUSION: Exogenous FM can produce a local hemostatic effect in the conditions of dosed experimental trauma and coagulopathy induced by warfarin intake. The hemostatic effect was mediated by intense thrombosis on the wound surface with the active recruitment of platelets in the process. The peculiarities of the demonstrated effects of FM may be mediated though the mechanisms of its action that have not yet been identified, which necessitates continuation of the research in this direction.
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