egcg激活nrf2are通路对液压冲击脑损伤的神经保护作用及其机制word格式论文.docxVIP

egcg激活nrf2are通路对液压冲击脑损伤的神经保护作用及其机制word格式论文.docx

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egcg激活nrf2are通路对液压冲击脑损伤的神经保护作用及其机制word格式论文

目录中文摘要···········································································································1英文摘要···········································································································5英文缩写·········································································································10研究论文EGCG激活Nrf2-ARE通路对液压冲击脑损伤的神经保护作用及其机制前言··········································································································11材料与方法······························································································13结果·········································································································24附图··········································································································27附表··········································································································42讨论··········································································································47结论··········································································································52参考文献··································································································53综述EGCG 抗氧化性质及其对中枢神经系统疾病的保护作用57致谢··············································································································71个人简历··········································································································72EGCG激活Nrf2-ARE通路对液压冲击脑损伤的神经保护作用及其机制摘要目的:通过观察表没食子儿茶素没食子酸酯(EGCG)对液压冲击脑损伤后核因子E2相关因子2(Nrf2)、caspase-3、caspase-12及炎性细胞因子表达变化的影响,探讨EGCG在液压冲击脑损伤所发挥的抗凋亡、抗炎的神经保护作用及其机制。方法:1体重为250g±50g的成年雄性SD大鼠24只,随机分成3组:假手术组(ShamGroup)、脑损伤溶媒组(TBI+VehicleGroup)以及脑损伤干预组(TBI+EGCGGroup),每组8只。后两组均实施麻醉后,于颅骨矢状缝右侧、冠状缝后约5mm处磨取骨窗,直径约4mm,常规行液压冲击,其中TBI+Vehicle组磨骨窗、液压冲击后给予腹腔注射生理盐水1ml,TBI+EGCG组磨骨窗、液压冲击后给予腹腔注射EGCG50mg/kg+1ml生理盐水;Sham组大鼠常规麻醉后,头颅磨除骨窗,保持硬膜完整,但不行液压冲击伤。2所有动物在24h进行mNSS神经功能缺损评分,并过度麻醉,断头处死后迅速开颅取出脑组织。在大鼠脑组织损伤区前部切取大约100mg,应用E

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