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凝血酶在血小板晚期血栓生长和/或稳定性中起关键作用。一种特异性凝血酶抑制剂对暴露于流动兔血的主动脉内皮下层诱导的血栓形成的影响。

Thrombin plays a key role in late platelet thrombus growth and/or stability. Effect of a specific thrombin inhibitor on thrombogenesis induced by aortic subendothelium exposed to flowing rabbit blood.

作者信息

Gast A, Tschopp T B, Baumgartner H R

机构信息

F. Hoffmann-La Roche Ltd, Pharmaceutical Division, Preclinical Research Department, Basel, Switzerland.

出版信息

Arterioscler Thromb. 1994 Sep;14(9):1466-74. doi: 10.1161/01.atv.14.9.1466.

Abstract

Thrombin is involved in the pathogenesis of venous and arterial thrombosis. This study addressed the question of the relative importance of thrombin in the early and late phases of thrombogenesis. The effect of Ro 46-6240 (1.43 mg/kg bolus and 0.1 mg/kg per minute i.v.), a novel, selective thrombin inhibitor on thrombogenesis induced by rabbit aorta subendothelium, was measured ex vivo in a perfusion chamber model after a short (5-minute) and long (30-minute) exposure time to rabbit native blood. The role of the perfusion time was assessed at shear rates of 100/s, 650/s, and 2600/s. These shear rates mimic blood flow conditions found in veins, arteries, and small or stenosed arteries, respectively. Fibrin deposition and platelet thrombus formation on subendothelium were evaluated by microscopic morphometry. In the presence of Ro 46-6240, fibrin deposition was abolished at both perfusion times and at all shear rates. In the 5-minute experiments, thrombus height was reduced by Ro 46-6240 at shear rates of 100/s (85%) and 650/s (35%) but not at a shear rate of 2600/s, whereas thrombus area was not affected at any shear rate. In contrast, both thrombus height and thrombus area were reduced (60% to 90%) by Ro 46-6240 in the 30-minute perfusion groups at all wall shear rates. The antithrombotic effect of Ro 46-6240 after 30-minute perfusion was confirmed by the minimal increase in the pressure difference between the entrance and the exit of the perfusion chamber compared with the control groups.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

凝血酶参与静脉和动脉血栓形成的发病机制。本研究探讨了凝血酶在血栓形成早期和晚期的相对重要性问题。在体外灌注室模型中,测量新型选择性凝血酶抑制剂Ro 46-6240(1.43 mg/kg静脉推注,随后0.1 mg/kg每分钟静脉输注)对兔主动脉内皮下诱导的血栓形成的影响,该模型在短(5分钟)和长(30分钟)暴露于兔全血后进行。在100/s、650/s和2600/s的剪切速率下评估灌注时间的作用。这些剪切速率分别模拟静脉、动脉以及小动脉或狭窄动脉中的血流状况。通过显微镜形态计量学评估内皮下的纤维蛋白沉积和血小板血栓形成。在Ro 46-6240存在的情况下,在所有灌注时间和所有剪切速率下,纤维蛋白沉积均被消除。在5分钟的实验中,Ro 46-6240在100/s(85%)和650/s(35%)的剪切速率下可降低血栓高度,但在2600/s的剪切速率下则无此作用,而在任何剪切速率下血栓面积均不受影响。相比之下,在30分钟灌注组中,Ro 46-6240在所有壁面剪切速率下均使血栓高度和血栓面积降低(60%至90%)。与对照组相比,灌注室进出口压力差的最小增加证实了Ro 46-6240在30分钟灌注后的抗血栓作用。(摘要截短于250字)

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