中国神经再生研究(英文版) ›› 2019, Vol. 14 ›› Issue (10): 1796-1804.doi: 10.4103/1673-5374.257534

• 原著:脑损伤修复保护与再生 • 上一篇    下一篇

两种严重创伤性脑损伤模型的病理变化差异

  

  • 出版日期:2019-10-15 发布日期:2019-10-15
  • 基金资助:

    国家自然科学基金(81671221)

Differences in pathological changes between two rat models of severe traumatic brain injury

Yi-Ming Song 1, 2, Yu Qian 1, 2, Wan-Qiang Su 1, 2, Xuan-Hui Liu 1, 2, Jin-Hao Huang 1, 2, Zhi-Tao Gong 1, 2, Hong-Liang Luo 1, 2, Chuang Gao 1, 2, Rong-Cai Jiang 1, 2   

  1. 1 Department of Neurosurgery, General Hospital, Tianjin Medical University, Tianjin, China
    2 Key Laboratory of Injuries, Variations and Regeneration of Nervous System, Tianjin Neurological Institute, Tianjin, China
  • Online:2019-10-15 Published:2019-10-15
  • Contact: Rong-Cai Jiang, PhD, jiang116216@163.com
  • Supported by:

    This study was supported by the National Natural Science Foundation of China, No. 81671221 (to RCJ)

摘要:

重型自由落体下降模型能模拟重型颅脑损伤造成的弥漫性轴索损伤,而重型控制性皮质撞击模型则能通过设定精确的打击参数来建立起重型颅脑损伤模型。为此,实验拟比较这两种模型的病理机制和病理变化来确定其造成的重型颅脑损伤的异同点。实验采用电子控制性皮质撞击装置建立重型控制性皮质撞击大鼠模型,通过塑料管引导从1.8 m高处使500 g重物自由垂直下落建立重型自由落体下降大鼠模型。实验记录了两种模型大鼠的体温和死亡率,通过改良大鼠神经功能缺损评分评估其神经功能损伤情况,通过脑水含量和伊文思蓝外渗实验来检测脑水肿和血脑屏障损伤情况。采用细胞因子阵列试剂盒检测各组损伤后的炎症反应情况,并用免疫荧光染色检测各组大脑和脑干神经细胞凋亡。结果显示:(1)重型控制性皮质撞击模型和重型自由落体下降模型均表现出明显的神经功能损伤和体温波动,重型控制性皮质撞击大鼠模型的运动功能损伤更严重,重型自由落体下降大鼠模型的认知功能损伤更严重;(2)重型控制性皮质撞击大鼠模型的脑水肿,炎症细胞因子改变和大脑神经细胞凋亡更为显着,血脑屏障损伤更集中;(3)重型自由落体下降大鼠模型表现出更明显的脑干神经元凋亡和弥漫性的血脑屏障损伤,死亡率更高,重复性更低;(4)上述结果表明,重型控制性皮质撞击大鼠模型更稳定,可重复率高,在短时间内即显示出明显的脑组织病理变化。相反,重型自由落体下降大鼠模型则表现出高死亡率,并有重型控制性皮质撞击中未表现的严重脑干损伤。因此,作者推测,重型控制性皮质撞击大鼠模型有助于临床重型颅脑损伤后的病理机制研究,而重型自由落体下降模型则侧重于临床弥漫性轴索损伤的基础动物研究。实验经天津医科大学动物伦理委员会批准(批准号IRB2012-028-02,批准时间:2012年2月)

orcid: 0000-0002-9119-0115 (Rong-Cai Jiang)

关键词: 重型颅脑损伤, 动物模型比较, 自由落体下降, 控制性皮质撞击, 神经功能损伤, 神经炎症, 血脑屏障损伤, 神经元凋亡, 弥漫性轴索损伤, 脑干损伤

Abstract:

The rat high-impact free weight drop model mimics the diffuse axonal injury caused by severe traumatic brain injury in humans, while severe controlled cortical impact can produce a severe traumatic brain injury model using precise strike parameters. In this study, we compare the pathological mechanisms and pathological changes between two rat severe brain injury models to identify the similarities and differences. The severe controlled cortical impact model was produced by an electronic controlled cortical impact device, while the severe free weight drop model was produced by dropping a 500 g free weight from a height of 1.8 m through a plastic tube. Body temperature and mortality were recorded, and neurological deficits were assessed with the modified neurological severity score. Brain edema and blood-brain barrier damage were evaluated by assessing brain water content and Evans blue extravasation. In addition, a cytokine array kit was used to detect inflammatory cytokines. Neuronal apoptosis in the brain and brainstem was quantified by immunofluorescence staining. Both the severe controlled cortical impact and severe free weight drop models exhibited significant neurological impairments and body temperature fluctuations. More severe motor dysfunction was observed in the severe controlled cortical impact model, while more severe cognitive dysfunction was observed in the severe free weight drop model. Brain edema, inflammatory cytokine changes and cortical neuronal apoptosis were more substantial and blood-brain barrier damage was more focal in the severe controlled cortical impact group compared with the severe free weight drop group. The severe free weight drop model presented with more significant apoptosis in the brainstem and diffused blood-brain barrier damage, with higher mortality and lower repeatability compared with the severe controlled cortical impact group. Severe brainstem damage was not found in the severe controlled cortical impact model. These results indicate that the severe controlled cortical impact model is relatively more stable, more reproducible, and shows obvious cerebral pathological changes at an earlier stage. Therefore, the severe controlled cortical impact model is likely more suitable for studies on severe focal traumatic brain injury, while the severe free weight drop model may be more apt for studies on diffuse axonal injury. All experimental procedures were approved by the Ethics Committee of Animal Experiments of Tianjin Medical University, China (approval number: IRB2012-028-02) in February, 2012.

Key words: nerve regeneration, severe traumatic brain injury, animal model comparison, free weight drop, controlled cortical impact, neurological impairment, neuroinflammation, blood-brain barrier damage, neuronal apoptosis, diffuse axonal injury, brainstem injury, neural regeneration