Papadopoulos S M, Chandler W F, Salamat M S, Topol E J, Sackellares J C
J Neurosurg. 1987 Sep;67(3):394-8. doi: 10.3171/jns.1987.67.3.0394.
Systemic fibrinolytic therapy for acute stroke is no longer recommended because of resulting systemic fibrinolysis and the risk of intracerebral hemorrhage. Human tissue-type plasminogen activator (TPA) is a native enzyme that converts plasminogen to plasmin with subsequent clot lysis. The affinity for plasminogen is increased several-fold when the substrate is bound to fibrin. At appropriate dosage, "clot-specific" thrombolysis may be achieved at the surface of the thrombus without creating systemic fibrinolysis. The authors designed a study to evaluate the effect of intravenous TPA administered 2 hours after acute thromboembolic stroke in rats. This time course was chosen to simulate an analogous clinical situation. Middle cerebral artery embolic stroke was caused by intracarotid injection of 0.025 cc of human blood clot in 16 rats. Regional cerebral blood flow, measured by the hydrogen clearance technique, and electroencephalographic (EEG) recordings were obtained every 30 minutes for 5 hours after thromboembolism. Eight rats received a 1-hour infusion of intravenous TPA (1.5 mg/kg) 2 hours after injection of emboli. Ipsilateral blood flow increased significantly within 30 minutes after intravenous TPA and reached preembolic levels within 60 minutes. Blood flow did not improve in the eight control rats throughout the experiment. Power spectral analysis of the EEG recordings showed improvement in the treated group compared to the control group. Postmortem angiography revealed proximal middle cerebral artery occlusion in control animals and patent middle cerebral arteries in TPA-treated animals. Serum fibrinogen and fibrin split products were unchanged in both groups, indicating the absence of systemic fibrinolysis. There were no intracerebral hemorrhages. It is concluded that, in this rat model, TPA increases blood flow with subsequent improvement in the EEG recording after thromboembolic stroke without evidence of systemic fibrinolysis. Intravenous TPA may be useful in the treatment of acute stroke in man.
由于会导致全身纤溶以及颅内出血风险,急性中风的全身纤溶疗法已不再被推荐。人组织型纤溶酶原激活剂(TPA)是一种天然酶,可将纤溶酶原转化为纤溶酶,随后使血栓溶解。当底物与纤维蛋白结合时,对纤溶酶原的亲和力会增加几倍。在适当剂量下,可在血栓表面实现“凝块特异性”溶栓,而不会引发全身纤溶。作者设计了一项研究,以评估急性血栓栓塞性中风2小时后静脉注射TPA对大鼠的影响。选择这个时间过程来模拟类似的临床情况。通过颈内动脉注射0.025立方厘米人血凝块,在16只大鼠中造成大脑中动脉栓塞性中风。在血栓栓塞后5小时内,每30分钟通过氢清除技术测量局部脑血流量,并进行脑电图(EEG)记录。8只大鼠在注射栓子2小时后接受了1小时的静脉TPA输注(1.5毫克/千克)。静脉注射TPA后30分钟内,同侧血流量显著增加,并在60分钟内达到栓塞前水平。在整个实验过程中,8只对照大鼠的血流量没有改善。EEG记录的功率谱分析显示,治疗组与对照组相比有所改善。死后血管造影显示,对照动物大脑中动脉近端闭塞,而TPA治疗动物大脑中动脉通畅。两组的血清纤维蛋白原和纤维蛋白降解产物均未改变,表明没有全身纤溶。没有颅内出血。得出的结论是,在这个大鼠模型中,TPA可增加血流量,随后在血栓栓塞性中风后改善EEG记录,且没有全身纤溶的证据。静脉注射TPA可能对人类急性中风的治疗有用。