世界中医药
文章摘要
引用本文:徐立,宋文婷,任建勋,王光蕊,朱盛,姚明江,侯金才,刘建勋.结扎颈总动脉复合低氧致C 57 BL/6小鼠缺血缺氧性脑病模型的建立及溶栓胶囊的作用[J].世界中医药,2018,(01):.  
结扎颈总动脉复合低氧致C 57 BL/6小鼠缺血缺氧性脑病模型的建立及溶栓胶囊的作用
Establishment of C 57 BL/6 Mice of Hypoxic-ischemic Encephalopathy (HIE) Model by Arteria Carotis Communis Ligation Combined with Hypoxia Inhalation and Effects of Rongshuan Capsules
投稿时间:2017-12-20  
DOI:10.3969/j.issn.1673-7202.2018.01.004
中文关键词:  缺血缺氧性脑病  模型  肌力  学习记忆  溶栓胶囊
English Keywords:Hypoxic-ischemic encephalopathy (HIE)  Animal models  Muscle strength  Learning and memory  Rongshuan Capsules
基金项目:国家科技重大专项“重大新药创制”(2017ZX09301018);国家自然科学基金项目(81603617)
作者单位
徐立,宋文婷,任建勋,王光蕊,朱盛,姚明江,侯金才,刘建勋 中国中医科学院西苑医院基础医学研究所,中药药理北京市重点实验室,北京,100091 
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中文摘要:
      目的:通过结扎颈总动脉复合低氧建立C 57 BL/6小鼠缺血缺氧性脑病(HIE)的模型,并观察溶栓胶囊的作用。方法:C 57 BL/6小鼠随机分为假手术组、模型组、溶栓胶囊大、中、小剂量组(400、200、100 mg生药/kg)。采用左侧颈总动脉结扎并通入氧气和氮气(8:92)15 min的方法,建立C 57 BL/6小鼠缺血缺氧性脑病模型。在缺血缺氧损伤24 h后开始灌胃给药,1次/d,连续给药4周。4周后观察模型小鼠肌力、学习记忆能力的改变以及脑组织病理形态学变化以及NSE、MAP-2和Caspase-3的表达。结果:手术后4周,缺血缺氧性脑病C 57 BL/6小鼠肌力和学习记忆能力显著下降,NSE和MAP-2低表达,Caspase-3高表达,病理学检查可见神经元细胞排列紊乱,大量变性、坏死及凋亡细胞,另见大片软化灶,血管扩张充血,多量炎性反应细胞浸润。溶栓胶囊对上述指标有明显改善作用。结论:通过结扎颈总动脉合并低氧成功建立了C 57 BL/6小鼠缺血缺氧性脑病模型,溶栓胶囊可改善模型小鼠肌力、学习记忆下降等症状,减轻脑组织病理性损伤,其机制可能与其神经保护作用有关。
English Summary:
      To establish hypoxic-ischemic encephalopathy (HIE) model on C 57 BL/6 mice by carotid artery ligation and hypoxia inhalation, and to observe the effect of Rongshuan Capsules. Methods: C 57 BL/6 mice were randomly divided into 5 groups: sham-operation group, model group, large dosage of Rongshuan Capsules, middle dosage of Rongshuan Capsules, and small dosage of Rongshuan Capsules (400 mg/kg, 200 mg/kg and 100 mg/kg). HIE model mice were established by left carotid artery ligation on C 57 BL/6 mice and hypoxia inhalation (O2:N2 = 8:92) for 15 minutes. Intragastric administration was used on HIE model mice 24 hours after ischemia anoxic damage, 1 time/day and consecutively treated for 4 weeks. After 4 weeks of treatment, muscle strength, ability of learning and memory, NSE, MAP-2 and Caspase-3 expression and the brain tissue pathomorphological changes were tested. Results: Four weeks after model establishment, muscle strength and learning and memory ability of HIE model mice were decreased significantly. MAP-2 and NSE expression was down-regulated, and Caspase-3 expression was up-regulated. Pathological examination showed that neurons were arranged in disorders, large amount of degenerated, necrotic and apoptotic cells. Large pieces of softening lesion, expansion and congestion of vessels and inflammatory cell infiltration were also observed. Rongshuan Capsules improved these indexes significantly in drug administration groups. Conclusion: Caroted artery ligation with hypoxia successfully established HIE models on C 57 BL/6 mice. Rongshuan Capsules facilitated model mice of muscle strength and learning and memory ability as well as MAP-2 and Caspase-3 expression, release the pathological injury of brain tissues, whose mechanism may be related to its neural protection.
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