Yu Xinge, Li Yang V
Department of Biomedical Sciences, Ohio University, Athens, OH, 45701, USA.
Program in Biological Sciences, Ohio University, 346 Irvine Hall, Athens, OH, 45701, USA.
Acta Neurochir Suppl. 2016;121:115-9. doi: 10.1007/978-3-319-18497-5_20.
Thrombotic cerebral ischemia is one of the leading causes of mortality and chronic disability. Animal models provide an essential tool for understanding the complex cellular and molecular pathophysiology of ischemia and for improving treatment and testing novel neuroprotective drugs in the preclinical setting. In this study, we tested zebrafish as a novel model for thrombotic ischemic brain damage. Zebrafish were intraperitoneally injected with Rose Bengal and light exposure was directed onto the optic tectum region of the brain to induce photothrombosis. After full recovery from anesthesia, zebrafish consistently exhibited abnormal swimming patterns, indicating brain injury from the procedure. The staining of 2,3,5-triphenyltetrazolium chloride (TTC) 24 h after the treatment showed lack of staining of the exposed area of the brain, which further confirmed the ischemic injury. Application of Activase®-tPA improved viability of the brain. The tPA treatment also reduced the occurrence of moving disability as well as the mortality rate, demonstrating that the zebrafish model not only showed focal ischemic injury but also responded well to tPA therapy. Our results suggest that the current photothrombotic method induced focal ischemia in zebrafish and produced consistent brain damage that can be measured by behavioral changes and quantified by histological staining.
血栓性脑缺血是导致死亡和慢性残疾的主要原因之一。动物模型为理解缺血复杂的细胞和分子病理生理学,以及在临床前环境中改进治疗方法和测试新型神经保护药物提供了重要工具。在本研究中,我们测试了斑马鱼作为血栓性缺血性脑损伤的新型模型。给斑马鱼腹腔注射孟加拉玫瑰红,并将光照直接照射到脑的视顶盖区域以诱导光血栓形成。从麻醉中完全恢复后,斑马鱼持续表现出异常的游泳模式,表明该操作导致了脑损伤。处理后24小时的2,3,5-三苯基氯化四氮唑(TTC)染色显示脑暴露区域无染色,这进一步证实了缺血性损伤。应用阿替普酶(Activase®-tPA)可提高脑的存活率。tPA治疗还降低了行动障碍的发生率以及死亡率,表明斑马鱼模型不仅显示出局灶性缺血损伤,而且对tPA治疗反应良好。我们的结果表明,当前的光血栓形成方法在斑马鱼中诱导了局灶性缺血,并产生了可通过行为变化测量和通过组织学染色量化的一致脑损伤。