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阿加曲班在兔实验性血栓形成中的抗血栓活性。

Antithrombotic activity of argatroban in experimental thrombosis in the rabbit.

作者信息

Berry C N, Girard D, Girardot C, Lochot S, Lunven C, Visconte C

机构信息

Cardiovascular Department, Synthélabo Recherche, Bagneux, France.

出版信息

Semin Thromb Hemost. 1996;22(3):233-41. doi: 10.1055/s-2007-999013.

Abstract

Argatroban was evaluated in three models of thrombosis in the rabbit: the Wessler model (thromboplastin plus stasis of the left jugular vein), an arteriovenous shunt model, and a model of arterial thrombosis induced by endothelial and intimal damage of the left femoral artery. Calcium heparin was used as a comparator. Both substances inhibited thrombus formation in the Wessler model with ID50 values of 0.32 and 0.16 mg/kg intravenous bolus for argatroban and heparin respectively, with similar changes in thrombin time (4 to 5 times control) and activated partial thromboplastin time (APTT) (1.6 to 2.1 times control) for both substances at antithrombotic doses. The ID50 values of both substances were 2.4 micrograms/kg/min (argatroban) and 0.5 microgram/kg/min (heparin). When they were administered by continuous infusion, no significant effects on the APTT were noted. In the arteriovenous shunt, the ID50 values for argatroban and heparin (respectively) were 0.16 and 0.07 mg/kg intravenous bolus, and 4.5 and 2.8 micrograms/kg/min intravenous infusion. Vessel clamping followed immediately by electrical stimulation (5 mA direct current, 5 minutes) of the left femoral artery leads to the formation of an occlusive thrombus approximately 30 minutes after clamping. Argatroban infused for 60 minutes before the vascular lesion and throughout the 90 minute observation period led to a dose-dependent delay in arterial occlusion with significant effects seen at 5 micrograms/kg/min with five of eight animals showing normal femoral blood flow at 90 minutes postlesion at 20 micrograms/kg/min; no significant increases (Dunnett's test) in APTT were noted with argatroban. Heparin was without effect even at 40 micrograms/kg/min, despite an eight-fold increase in APTT at 20 micrograms/kg/min and values of more than 300 seconds at 40 micrograms/kg/min. Thus, in models of arterial but not venous thrombosis, argatroban is a more potent antithrombotic agent than heparin on a weight basis, with antithrombotic effects at a much lower degree of systemic anticoagulation.

摘要

在兔的三种血栓形成模型中对阿加曲班进行了评估

韦氏勒模型(凝血活酶加左颈静脉血流淤滞)、动静脉分流模型以及由左股动脉内皮和内膜损伤诱导的动脉血栓形成模型。使用钙肝素作为对照物。两种物质在韦氏勒模型中均抑制血栓形成,阿加曲班和肝素静脉推注的ID50值分别为0.32和0.16mg/kg,在抗血栓剂量下,两种物质的凝血酶时间(为对照值的4至5倍)和活化部分凝血活酶时间(APTT)(为对照值的1.6至2.1倍)有相似变化。两种物质的ID50值分别为2.4微克/千克/分钟(阿加曲班)和0.5微克/千克/分钟(肝素)。当通过持续输注给药时,未观察到对APTT有显著影响。在动静脉分流模型中,阿加曲班和肝素的ID50值(分别)为静脉推注0.16和0.07mg/kg,静脉输注4.5和2.8微克/千克/分钟。立即夹住血管并随后对左股动脉进行电刺激(5毫安直流电,5分钟)会在夹住后约30分钟导致闭塞性血栓形成。在血管损伤前输注阿加曲班60分钟并在整个90分钟观察期内持续输注,导致动脉闭塞出现剂量依赖性延迟,在5微克/千克/分钟时出现显著效果,在损伤后90分钟时,八只动物中有五只在20微克/千克/分钟时股动脉血流正常;使用阿加曲班未观察到APTT有显著升高(邓尼特检验)。即使在40微克/千克/分钟时肝素也无作用,尽管在20微克/千克/分钟时APTT增加了八倍,在40微克/千克/分钟时APTT值超过300秒。因此,在动脉血栓形成模型而非静脉血栓形成模型中,按重量计算阿加曲班是比肝素更有效的抗血栓药物,在全身抗凝程度低得多的情况下即具有抗血栓作用。

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