Department of Neurology, Yonsei University College of Medicine, Seoul, Korea ; Severance Integrative Research Institute for Cerebral and Cardiovascular Diseases, Yonsei University College of Medicine, Seoul, Korea ; Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Korea.
PLoS One. 2013 Nov 18;8(11):e81165. doi: 10.1371/journal.pone.0081165. eCollection 2013.
Saxatilin, a novel disintegrin purified and cloned from the venom of the Korean snake Gloydius saxatilis, strongly inhibits activation and aggregation of platelets. Glycoprotein (GP) IIb/IIIa receptor antagonists can resolve thrombus, so saxatilin might also have thrombolytic effects. We investigated the thrombolytic effects of saxatilin in mice using a ferric chloride-induced carotid arterial thrombosis model. Thrombotic occlusion and thrombus resolution were evaluated quantitatively by measuring blood flow in the carotid artery with an ultrasonic flow meter and calculating the degree of flow restoration on a minute-by-minute basis; results were confirmed by histological examination. Saxatilin dissolved thrombi in a dose-dependent manner. Saxatilin at 5 mg/kg restored blood flow to baseline levels. As saxatilin dose increased, time to recanalization decreased. A bolus injection of 10% of a complete dose with continuous infusion of the remaining dose for 60 minutes resulted in effective recanalization without reocclusion. The thrombolytic effect of saxatilin was also demonstrated in vitro using platelet aggregometry by administering saxatilin in preformed thrombi. Bleeding complications were observed in 2 of 71 mice that received saxatilin. Fibrin/fibrinogen zymography and platelet aggregometry studies indicated that saxatilin does not have fibrinolytic activity, but exerted its action on platelets. Integrin-binding assays showed that saxatilin inhibited multiple integrins, specifically α2bβ3 (GP IIb/IIIa), α5β1, αvβ3, αvβ1, and αvβ5, which act on platelet adhesion/aggregation. Saxatilin inhibited multiple integrins by acting on platelets, and was safe and effective in resolving thrombi in mice.
沙甲凝素是从韩国蛇(Gloydius saxatilis)毒液中纯化和克隆的一种新型解整合素,强烈抑制血小板的激活和聚集。糖蛋白(GP)IIb/IIIa 受体拮抗剂可溶解血栓,因此沙甲凝素可能也具有溶栓作用。我们用氯化铁诱导的颈动脉血栓形成模型研究了沙甲凝素在小鼠体内的溶栓作用。用超声流量计测量颈动脉血流来定量评估血栓形成和血栓溶解情况,并根据每分钟的恢复程度计算血流恢复程度;通过组织学检查进行了验证。沙甲凝素呈剂量依赖性溶解血栓。沙甲凝素 5mg/kg 可使血流恢复至基线水平。随着沙甲凝素剂量的增加,再通时间缩短。给予 10%的全剂量的推注,并持续输注剩余剂量 60 分钟,可有效再通而无再闭塞。通过在已形成的血栓中给予沙甲凝素,在体外的血小板聚集测定中也观察到了沙甲凝素的溶栓作用。71 只接受沙甲凝素的小鼠中有 2 只出现出血并发症。纤维蛋白原/纤维蛋白溶酶图谱和血小板聚集测定研究表明,沙甲凝素没有纤维蛋白溶解活性,而是对血小板起作用。整合素结合测定表明,沙甲凝素抑制多种整合素,特别是α2bβ3(GP IIb/IIIa)、α5β1、αvβ3、αvβ1 和αvβ5,这些整合素作用于血小板的黏附和聚集。沙甲凝素通过作用于血小板抑制多种整合素,在小鼠体内安全有效地溶解血栓。