Ye Yang, Xin Xi-Yan, Zhang Hao-Lin, Fan Rui-Wen, Zhu Yu-Tian, Li Dong
Department of Traditional Chinese Medicine, Peking University Third Hospital, Beijing 100191, China.
Department of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University, Beijing 100191, China.
Heliyon. 2023 Jan 19;9(1):e13102. doi: 10.1016/j.heliyon.2023.e13102. eCollection 2023 Jan.
To establish a new mouse model of haemorrhagic transformation associated with delayed tissue-type plasminogen activator (tPA) treatment to provide a novel tool to study therapeutic strategies for haemorrhagic transformation.
Male C57BL/6 mice were subjected to carotid artery thrombosis stimulated with ferric chloride. The thrombus was then mechanically detached to induce migration toward the intracranial circulation. To induce haemorrhagic transformation, mice were intravenously injected with 10 mg/kg tPA 4.5 h after the onset of ischaemia and were sacrificed 24 h after tPA treatment.
In this new model, administration of tPA 4.5 h after stroke exacerbated the risk of intracerebral haemorrhage. Thrombolysis with tPA also exacerbated cerebral infarction, brain oedema, blood-brain barrier breakdown, and neurological deficits. However, cerebral blood flow was not significantly affected.
The present model is reproducible, easy to perform, and mimics the clinical situation of haemorrhagic transformation after tPA treatment in humans. This modified model can be used as a new tool to test experimental drugs for haemorrhagic transformation associated with delayed tPA administration after an ischaemic stroke.
建立一种与延迟组织型纤溶酶原激活剂(tPA)治疗相关的出血转化小鼠新模型,为研究出血转化的治疗策略提供一种新工具。
雄性C57BL/6小鼠接受氯化铁刺激的颈动脉血栓形成。然后机械分离血栓以诱导其向颅内循环迁移。为诱导出血转化,在缺血发作4.5小时后给小鼠静脉注射10mg/kg tPA,并在tPA治疗后24小时处死小鼠。
在这个新模型中,中风后4.5小时给予tPA会增加脑出血风险。tPA溶栓还会加重脑梗死、脑水肿、血脑屏障破坏和神经功能缺损。然而,脑血流量未受到显著影响。
本模型具有可重复性、易于操作,且模拟了人类tPA治疗后出血转化的临床情况。这种改良模型可作为一种新工具,用于测试针对缺血性中风后延迟给予tPA相关出血转化的实验药物。