Mehta J L, Chen L, Nichols W W, Johannesen M, Bregengård C, Hedner U, Saldeen T G
Department of Medicine, University of Florida College of Medicine, Gainesville 32610-0277.
J Am Coll Cardiol. 1995 Mar 1;25(3):753-60. doi: 10.1016/0735-1097(94)00444-u.
This study examined the modification of recombinant tissue-type plasminogen activator (rt-PA)-induced thrombolysis by recombinant lys-plasminogen.
Recombinant tissue-type plasminogen activator restores flow in the thrombosed coronary artery, but the artery often reoccludes. The rt-PA-induced thrombolysis is a result of activation of plasminogen bound to fibrin in the thrombus and results in generation of the fibrinolytic enzyme plasmin. Small amounts of lys-plasminogen are formed when rt-PA is used. Lys-plasminogen binds to fibrin with a 10-fold greater affinity than the predominant native glu-plasminogen, leading to a loose fibrin structure.
Dogs with electrically induced occlusive intracoronary thrombus were treated with saline solution (n = 9), glu-plasminogen (2 mg/kg body weight, n = 5) or lys-plasminogen (2 mg/kg, n = 5), followed by infusion of rt-PA (1 mg/kg over 20 min) 10 min later.
Reperfusion rates were similar in all groups of dogs, but the time to reflow was lowest in dogs given lys-plasminogen compared with those given saline solution or glu-plasminogen before rt-PA (mean [+/- SE] 14 +/- 2 vs. 22 +/- 2 and 23 +/- 3 min, respectively, p < 0.05). None of the reperfused coronary arteries reoccluded in the lys-plasminogen plus rt-PA group, whereas 75% reoccluded in dogs given saline solution plus rt-PA, and 50% reoccluded in those given glu-plasminogen plus rt-PA. Accordingly, duration of reflow was greater in the lys-plasminogen plus rt-PA group (> 120 vs. 39 +/- 7 and 82 +/- 21 min, respectively, p < 0.05). Plasminogen activator inhibitor-1 activity decreased during rt-PA infusion and thereafter increased in all dogs, but less so in dogs given lys-plasminogen (p < 0.05 vs. those given saline solution before rt-PA).
Treatment with recombinant lys-plasminogen before rt-PA reduces time to reflow and sustains reflow after thrombolysis, whereas glu-plasminogen has no such effect.
本研究检测了重组赖氨酸纤溶酶原对重组组织型纤溶酶原激活剂(rt-PA)诱导的溶栓作用的影响。
重组组织型纤溶酶原激活剂可恢复血栓形成的冠状动脉血流,但该动脉常再次闭塞。rt-PA诱导的溶栓是血栓中与纤维蛋白结合的纤溶酶原激活的结果,会产生纤溶酶。使用rt-PA时会形成少量赖氨酸纤溶酶原。赖氨酸纤溶酶原与纤维蛋白的结合亲和力比主要的天然谷氨酸纤溶酶原高10倍,导致纤维蛋白结构松散。
用电诱导冠状动脉闭塞性血栓的犬,分别给予生理盐水(n = 9)、谷氨酸纤溶酶原(2mg/kg体重,n = 5)或赖氨酸纤溶酶原(2mg/kg,n = 5),10分钟后再输注rt-PA(20分钟内1mg/kg)。
所有犬组的再灌注率相似,但与rt-PA前给予生理盐水或谷氨酸纤溶酶原的犬相比,给予赖氨酸纤溶酶原的犬再灌注时间最短(平均[±标准误]分别为14±2分钟、22±2分钟和23±3分钟,p<0.05)。赖氨酸纤溶酶原加rt-PA组再灌注的冠状动脉均未再次闭塞,而给予生理盐水加rt-PA的犬75%再次闭塞,给予谷氨酸纤溶酶原加rt-PA的犬50%再次闭塞。因此,赖氨酸纤溶酶原加rt-PA组的再灌注持续时间更长(分别>120分钟、39±7分钟和82±21分钟,p<0.05)。在rt-PA输注期间纤溶酶原激活物抑制剂-1活性降低,之后所有犬的该活性均升高,但给予赖氨酸纤溶酶原的犬升高幅度较小(与rt-PA前给予生理盐水的犬相比,p<0.05)。
rt-PA前用重组赖氨酸纤溶酶原治疗可缩短再灌注时间并维持溶栓后的再灌注,而谷氨酸纤溶酶原无此作用。