Jang I K, Gold H K, Leinbach R C, Fallon J T, Collen D
Cardiac Unit, Massachusetts General Hospital, Boston 02114.
Circ Res. 1990 Dec;67(6):1552-61. doi: 10.1161/01.res.67.6.1552.
The effects of heparin and the synthetic competitive thrombin inhibitor (2R,4R)-4-methyl-1-[N2-(3-methyl-1,2,3,4-tetrahydro-8-quinolinesulfon yl)-L-arginyl]-2-piperidinecarboxylic acid monohydrate (Argatroban) on thrombolysis with recombinant tissue-type plasminogen activator (rt-PA) was studied in groups of six or seven rabbits with arterial thrombosis. The model consisted of a whole-blood clot produced in a 1-cm isolated femoral arterial segment with superimposed endothelial damage and distal high-grade stenosis. rt-PA was injected as an intravenous bolus of 0.45 mg/kg body wt at 15-minute intervals until recanalization, or up to a maximum of four boluses. In seven rabbits given an intravenous injection of 17 mg/kg aspirin, rt-PA induced transient reflow in only one animal. In seven rabbits that received intravenous heparin (200 units/kg over 60 minutes), rt-PA administration produced reflow in five animals, which was persistent in two rabbits. Combined administration of aspirin and heparin in seven rabbits was associated with similar rt-PA-induced recanalization. rt-PA administration in six rabbits given intravenous Argatroban (100 micrograms/kg/min for 60 minutes) caused recanalization in five, with persistent patency in three. In six rabbits given aspirin and Argatroban, rt-PA caused recanalization in all, with persistent patency in five animals. Reflow occurred significantly more rapidly with Argatroban (14 +/- 7 minutes) than with heparin (35 +/- 11 minutes), reflow was obtained with fewer boluses of rt-PA in combination with Argatroban (median value of one bolus) than with heparin (median value, three boluses), and reocclusion after reflow was less frequent with Argatroban (0 of 11 versus 5 of 10 rabbits). Furthermore, the degree of thrombolysis determined by pathological analysis was significantly more extensive with Argatroban than with heparin, and patency persisted during a 3-hour observation period, despite elimination of Argatroban from the circulation. Thus, Argatroban, relative to heparin, enhances and sustains thrombolysis with rt-PA. It may offer promise as an adjunctive agent for thrombolytic therapy of arterial thrombosis.
在患有动脉血栓形成的每组六只或七只兔子中,研究了肝素和合成竞争性凝血酶抑制剂(2R,4R)-4-甲基-1-[N2-(3-甲基-1,2,3,4-四氢-8-喹啉磺酰基)-L-精氨酰基]-2-哌啶羧酸一水合物(阿加曲班)对重组组织型纤溶酶原激活剂(rt-PA)溶栓作用的影响。该模型由在一段1厘米长的孤立股动脉段中产生的全血凝块组成,伴有叠加的内皮损伤和远端高度狭窄。rt-PA以0.45毫克/千克体重的静脉推注剂量,每隔15分钟注射一次,直至再通,或最多注射四次推注剂量。在七只静脉注射17毫克/千克阿司匹林的兔子中,rt-PA仅在一只动物中诱导了短暂再通。在七只接受静脉注射肝素(60分钟内200单位/千克)的兔子中,给予rt-PA后五只动物出现再通,其中两只兔子的再通持续存在。七只兔子联合给予阿司匹林和肝素与rt-PA诱导的类似再通相关。在六只静脉注射阿加曲班(100微克/千克/分钟,持续60分钟)的兔子中给予rt-PA,五只出现再通,三只保持通畅。在六只给予阿司匹林和阿加曲班的兔子中,rt-PA使所有兔子均出现再通,五只动物保持通畅。与肝素(35±11分钟)相比,阿加曲班组再通发生得明显更快(14±7分钟),与肝素组(中位值为三次推注)相比,联合使用阿加曲班时rt-PA推注次数更少(中位值为一次推注)即可实现再通,且阿加曲班组再通后再闭塞的情况较少(11只兔子中0只,而10只兔子中有5只)。此外,通过病理分析确定的溶栓程度,阿加曲班组比肝素组明显更广泛,并且尽管阿加曲班已从循环中清除,但在3小时观察期内通畅情况持续存在。因此,相对于肝素,阿加曲班可增强并维持rt-PA的溶栓作用。它可能有望作为动脉血栓形成溶栓治疗的辅助药物。