冲程(发动机)
纤溶酶原激活剂
医学
病变
纤溶
纤溶酶原激活剂
组织纤溶酶原激活剂
溶栓
血脑屏障
内科学
药理学
麻醉
中枢神经系统
病理
心肌梗塞
机械工程
工程类
作者
Antoine Anfray,Camille Brodin,Antoine Drieu,Fanny Potzeha,Basile Dalarun,Véronique Agin,Denis Vivien,Cyrille Orset
标识
DOI:10.1016/j.expneurol.2021.113606
摘要
Tissue type Plasminogen Activator (tPA), named alteplase (Actilyse®) under its commercial form, is currently the only pharmacological treatment approved during the acute phase of ischemic stroke, used either alone or combined with thrombectomy. Interestingly, the commercial recombinant tPA (rtPA) contains two physiological forms of rtPA: the single chain rtPA (sc-rtPA) and the two-chains rtPA (tc-rtPA), with differential properties demonstrated in vitro. Using a relevant mouse model of thromboembolic stroke, we have investigated the overall effects of these two forms of rtPA when infused early after stroke onset (i.e. 20 min) on recanalization, lesion volumes, alterations of the integrity of the blood brain barrier and functional recovery. Our data reveal that there is no difference in the capacity of sc-rtPA and tc-rtPA to promote fibrinolysis and reperfusion of the tissue. However, compared to sc-rtPA, tc-rtPA is less efficient to reduce lesion volumes and to improve functional recovery, and is associated with an increased opening of the blood brain barrier. These data indicate better understanding of differential effects of these tPA forms might be important to ultimately improve stroke treatment.
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