Division of Brain Science, Department of Physiology, Kurume University School of Medicine, Kurume, Japan.
Department of Neurosurgery, Kurume University School of Medicine, Kurume, Japan.
Oxid Med Cell Longev. 2017;2017:6873281. doi: 10.1155/2017/6873281. Epub 2017 Nov 10.
The combination of alteplase, a recombinant tissue plasminogen activator, and edaravone, an antioxidant, reportedly enhances recanalization after acute ischemic stroke. We examined the influence of edaravone on the thrombolytic efficacy of alteplase by measuring thrombolysis using a newly developed microchip-based flow-chamber assay. Rat models of embolic cerebral ischemia were treated with either alteplase or alteplase-edaravone combination therapy. The combination therapy significantly reduced the infarct volume and improved neurological deficits. Human blood samples from healthy volunteers were exposed to edaravone, alteplase, or a combination of alteplase and edaravone or hydrogen peroxide. Whole blood was perfused over a collagen- and thromboplastin-coated microchip; capillary occlusion was monitored with a video microscope and flow-pressure sensor. The area under the curve (extent of thrombogenesis or thrombolysis) at 30 minutes was 69.9% lower in the edaravone-alteplase- than alteplase-treated group. The thrombolytic effect of alteplase was significantly attenuated in the presence of hydrogen peroxide, suggesting that oxidative stress might hinder thrombolysis. D-dimers were measured to evaluate these effects in human platelet-poor plasma samples. Although hydrogen peroxide significantly decreased the elevation of D-dimers by alteplase, edaravone significantly inhibited the decrease. Edaravone enhances alteplase-mediated thrombolysis, likely by preventing oxidative stress, which inhibits fibrinolysis by alteplase in thrombi.
阿替普酶,一种重组组织型纤溶酶原激活物,和依达拉奉,一种抗氧化剂,联合使用据称可以增强急性缺血性脑卒中后的再通。我们通过使用新开发的基于微芯片的流动室测定法测量溶栓作用,检查了依达拉奉对阿替普酶溶栓效果的影响。采用阿替普酶或阿替普酶-依达拉奉联合治疗栓塞性脑缺血大鼠模型。联合治疗显著减小了梗死体积并改善了神经功能缺损。将健康志愿者的人血样本暴露于依达拉奉、阿替普酶、阿替普酶-依达拉奉联合或过氧化氢。全血在涂覆有胶原蛋白和凝血酶原的微芯片上灌注;通过视频显微镜和流量压力传感器监测毛细血管闭塞。在 30 分钟时,依达拉奉-阿替普酶组的曲线下面积(血栓形成或溶栓的程度)比阿替普酶组低 69.9%。在存在过氧化氢的情况下,阿替普酶的溶栓作用显著减弱,表明氧化应激可能会阻碍溶栓。通过测量 D-二聚体来评估人血小板缺乏血浆样本中的这些作用。尽管过氧化氢显著降低了阿替普酶升高的 D-二聚体,但依达拉奉显著抑制了其降低。依达拉奉增强了阿替普酶介导的溶栓作用,可能是通过防止氧化应激来实现的,氧化应激会抑制血栓中的阿替普酶的纤维蛋白溶解作用。