Thomas G R, Thibodeaux H, Bennett W F, Refino C J, Badillo J M, Errett C J, Zivin J A
Department of Cardiovascular Research, Genentech Inc., South San Francisco, California.
J Pharmacol Exp Ther. 1993 Jan;264(1):67-73.
The dose-dependent effects of tissue-type plasminogen activator (t-PA) on the kinetics of cerebral clot lysis in a rabbit model of middle cerebral artery embolic stroke were investigated. The clots were formed in vitro and tagged with 99Tc for gamma-scintigraphic imaging. After embolization, groups of animals were treated with t-PA. Dose-response curves for the t-PA were generated, and in addition, long and short dosing schedules were assessed. The optimal doses for frequency and rate of cerebral clot lysis in this model are approximately 6.3 mg/kg given over 2 hr or 3.3 mg/kg given over 30 min. These dosing regimens for t-PA were accompanied by approximately 50% consumption of plasma plasminogen, fibrinogen and alpha 2-antiplasmin. Doses of t-PA on either side of this optimum caused attenuation in both the frequency and rate of cerebral clot lysis. Treatment with t-PA under either dosing regimen did not augment the frequency of hemorrhagic transformation, but the size of the resultant hemorrhage in those animals where intracranial bleeding occurred was reduced by 3.3 mg/kg t-PA given over 30 min.
研究了组织型纤溶酶原激活剂(t-PA)在大脑中动脉栓塞性中风兔模型中对脑血凝块溶解动力学的剂量依赖性效应。血凝块在体外形成并用99Tc标记用于γ闪烁成像。栓塞后,对动物组给予t-PA治疗。生成了t-PA的剂量反应曲线,此外,还评估了长给药方案和短给药方案。在该模型中,脑血凝块溶解频率和速率的最佳剂量约为2小时内给予6.3mg/kg或30分钟内给予3.3mg/kg。这些t-PA给药方案伴随着血浆纤溶酶原、纤维蛋白原和α2抗纤溶酶约50%的消耗。该最佳剂量两侧的t-PA剂量均导致脑血凝块溶解频率和速率降低。两种给药方案下用t-PA治疗均未增加出血转化的频率,但在发生颅内出血的动物中,30分钟内给予3.3mg/kg t-PA可使由此产生的出血大小减小。