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纸质出版:2016
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王哲,刘震,刘昕,倪怀亮,郑岩,毛玉莹,冯华.两种实验性大鼠脑出血模型的对比研究[J].陆军军医大学学报(原第三军医大学学报),2016,38(13):1494-1500.
Wang Zhe,Liu Zhen,Liu Xin,Ni Huailiang,Zheng Yan,Mao Yuying,Feng Hua.Comparison of 2 rat models of intracerebral hemorrhage, autoblood injection or collagenase injection[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(13):1494-1500.
王哲,刘震,刘昕,倪怀亮,郑岩,毛玉莹,冯华.两种实验性大鼠脑出血模型的对比研究[J].陆军军医大学学报(原第三军医大学学报),2016,38(13):1494-1500. DOI:
Wang Zhe,Liu Zhen,Liu Xin,Ni Huailiang,Zheng Yan,Mao Yuying,Feng Hua.Comparison of 2 rat models of intracerebral hemorrhage, autoblood injection or collagenase injection[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(13):1494-1500. DOI:
目的 研究自体血和胶原酶两种脑出血造模方法对大鼠神经预后血脑屏障通透性及胶质瘢痕增生情况的影响。 方法 144只成年健康雄性SD大鼠,分为自体血组和胶原酶组两组,并按预设时间点(3、7、14、21 d
n=6)观察大鼠Bederson评分、伊文思蓝渗透性、脑含水量、HE染色和免疫组化荧光染色。 结果 Bederson评分、伊文思蓝渗透性和脑含水量结果显示,两组的神经预后及血脑屏障通透性均随时间恢复正常,而胶原酶组与自体血组相比,Bederson评分、伊文思蓝渗透量和脑含水量在第3、7、14天均明显升高(P0.05);HE染色结果说明,两组均随时间增加存在血肿吸收,炎症渗出,胶质瘢痕形成情况,而在第14天和第21天,自体血组较胶原酶组相比,血肿基本吸收完毕,炎症渗出及胶质瘢痕形成较少;免疫组化染色结果表示,两组血肿周围的胶质细胞原纤维酸性蛋白(glial fibrillary acidic protein
GFAP)表达随时间增加,但第7天和第14天胶原酶模型组GFAP表达水平更高。 结论 与自体血模型相比,胶原酶模型的神经功能损伤恢复过程更慢,同时血脑屏障破坏更严重,胶质瘢痕形成更明显,大鼠胶原酶注射模型更适合长时程的临床脑出血研究。
Objective To determine the effects of 2 rat models of experimental intracerebral hemorrhage (ICH) (collagenase infusion and autoblood infusion) on neurological outcome
permeability of blood-brain barrier and glial scar hyperplasia. Methods A total of 144 male Sprague-Dawley rats were randomly and equally divided into 2 groups
autoblood injection model or collagenase injection model. According to the preset-time (3
7
14 and 21 d after ICH
n=6 for each time point)
several indexes including Bederson scores
Evans blue permeation
brain dry-wet ratio
HE staining and immunohistochemical assay were assessed comprehensively. Results Bederson scores
Evans blue permeation and water content of perihematoma revealed that the neurological outcome and blood brain barrier permeability were gradually returned to normal with time elapse in the both models. Compared with the autoblood injection model
bederson scores
Evans blue permeation and water content of perihematoma were obviously increased in the collagenase injection model at the time points of 3
7 and 14 d (P0.05). HE staining results showed that the hematoma absorption
inflammatory exudation
and glial scar formation were enhanced in both models with time elapse. As compared with the collagenase injection model
more hematoma absorption
less inflammatory exudation and less glial scar formation were observed in the brain tissue of the autoblood injection model in 14 and 21 d after injection. Immunohistochemical staining showed that the expression of glial fibrillary acidic protein (GFAP) was increased with time elapse in the perihematoma region of the both models
with the highest levels in the collagenase injection model at 7 and 21 d. Conclusion As compared with the autoblood injection model
poorer neurological outcome
worse blood brain barrier breakdown and more glial scar formation are seen in the collagenase injection model. So this model is more suitable for long-term clinical study of cerebral hemorrhage.
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