首页|基于PERK-eIF2α-NF-κB信号通路研究苁蓉散治疗阿尔茨海默病的作用机制

基于PERK-eIF2α-NF-κB信号通路研究苁蓉散治疗阿尔茨海默病的作用机制

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目的 基于PERK-eIF2α-NF-κB信号通路研究苁蓉散治疗阿尔茨海默病(Alzheimer's disease,AD)的作用机制.方法 将60只SD大鼠分为正常组,模型组、苁蓉散组(4.62、9.24、18.48 g·kg-1)和安理申组,每组10只.除正常组外其余大鼠组予双侧海马注射Aβ1-42建立AD模型.灌胃结束后进行水迷宫行为学检测学习记忆能力;尼氏染色观察神经元及尼氏小体变化;免疫荧光检测NF-κB核转移情况;透射电镜观察大鼠海马区内质网形态;酶免疫测定Aβ1-42及炎症因子含量;Western blot 检测 PERK、eIF2α、NF-κB的蛋白表达水平.结果 水迷宫结果显示,苁蓉散能提高AD大鼠的逃避潜伏期时间、增加穿越求生平台次数、延长目标象限停留时间(P<0.05或P<0.01);尼氏染色结果显示,苁蓉散各剂量组神经元细胞排列较整齐,胞核存在,尼氏小体较为丰富;免疫荧光表明,苁蓉散可降低AD大鼠脑内NF-κB入核表达(P<0.05或P<0.01);透射电镜结果显示,苁蓉散各剂量组内质网形态整齐、未见明显扩张,结构正常;ELISA结果表明,苁蓉散可降低AD海马中的Aβ1-42,IL-1,TNF-α的含量;Western blot结果显示,苁蓉散各剂量组p-PERK/PERK,p-eIF2α/eIF2α,p-NF-κB p65/NF-κB p65 的蛋白比值明显下降(P<0.05或P<0.01).结论 苁蓉散可通过抑制PERK-eIF2α-NF-κB信号通路的活化,缓解神经元细胞ERS状态下免疫炎症反应,以改善AD大鼠的认知功能.
Mechanism of action for the treatment of Cong Rong San in the Alzheimer's disease based on PERK-eIF20e-NF-κB signaling pathway
Aim To explore the mechanism of Cong Rong San on AD model rats based on protein kinase R-like endoplasmic reticulum kinase(PERK)-eukaryotic initiation factor 2α(eIF2α)-nuclear factor kappa B(NF-κB)signaling pathway.Methods Sixty mice were randomly divided into normal group,model group,Cong Rong San groups(4.62,9.24,18.48 g·kg-1)and donepezil group,with 10 mice in each group.All groups of rats received bilateral hippocampal injections of Aβ1-42 to establish the AD model,except the normal group.After the intragastric administration,the Morris water maze behavior test was performed for rats to test-ed the learning and memory abilities.Nissl staining was detected the quantity and Nissl bodies of nerve cells.To detect the nuclear translocation of NF-κB by immu-nofluorescence.To observe the ultrastructure of endo-plasmic reticulum by Transmission electron microsco-py.ELISA for Aβ1-42 and inflammatory cytokines quantification.Western blot was used to detect the ex-pression level of protein in the hippocampus in PERK-eIF2α-NF-κB signaling pathway.Results The morris water maze results showed that Cong Rong San im-proved the escape latency time,increased the number of platform crossings,and prolonged the time spent in the target quadrant in AD rats.(P<0.05 or P<0.01).Nissl staining shows the neuronal cells are ar-ranged neatly,nucleus are present and the number of Nissl bodies was numerous and the number of neurons was increased in various doses of Cong Rong San.Im-munofluorescence showed that the expression of NF-κB in the nucleus of rats was decreased(P<0.05 or P<0.01).The shape of endoplasmic reticulum was neat,no significantly expanded,and the structure was normal in various doses of Cong Rong San.The levels of Aβ1-42,IL-1,TNF-α and the ratio of p-PERK/PERK,p-eIF2α/eIF2α,p-NF-κB p65/NF-κB p65 in hippo-campus of Cong Rong San group was significantly de-creased in ELISA and Western blot test(P<0.05 or P<0.01).Conclusion Cong Rong San can alleviates the immune inflammatory response of neuronal cells in the ERS state for improve the learning and memory a-bility of AD rats,the mechanism of action may through restraint the activation of PERK-eIF2α-NF-κB signa-ling pathway.

Alzheimer's diseaseCong Rong Sanen-doplasmic reticulum stressPERK-eIF2α-NF-κB sig-naling pathwayinflammatoryAβ1-42

王曦、龙清华、蔡元钦、王政喻、陈显兵、曾楚华

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湖北民族大学医学部,湖北恩施 445000

湖北民族大学风湿性疾病发生与干预湖北省重点实验室,湖北恩施 445000

云南中医药大学基础医学院,云南 昆明 650000

阿尔兹海默病 苁蓉散 内质网应激 PERK-eIF2α-NF-κB信号通路 炎症 Aβ1-42

2025

中国药理学通报
中国药理学会

中国药理学通报

北大核心
影响因子:1.54
ISSN:1001-1978
年,卷(期):2025.41(1)