首页|黄连解毒汤对APP/PS1转基因小鼠大脑皮质中TREM2/Akt/GSK3β通路的影响

黄连解毒汤对APP/PS1转基因小鼠大脑皮质中TREM2/Akt/GSK3β通路的影响

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基于"毒损脑络"阿尔茨海默病(Alzheimer's disease,AD)中医病机,黄连解毒汤治疗AD的机制还不清楚.该研究旨在探讨黄连解毒汤调节髓样细胞触发受体2(triggering receptor expressed on myeloid cells 2,TREM2)/苏氨酸蛋白激酶(protein kinase B,Akt)/糖原合酶激酶3β(glycogen synthase kinase 3β,GSK3β)通路改善APP/PS1转基因小鼠认知障碍机制.将9月龄APP/PS1小鼠采用随机数字表法分为模型组,黄连解毒汤低、中、高(2.5、5、10 g·kg-1)组和盐酸多奈哌齐0.75 mg·kg-1组,同月龄C57BL/6J小鼠为正常组.连续给药1个月后,采用Morris水迷宫检测小鼠的学习记忆能力,苏木素-伊红(HE)染色观察小鼠皮质区神经细胞形态,免疫荧光检测β淀粉样蛋白(β-amyloid,Aβ)1-42、CD86及精氨酸酶1(arginase 1,Arg1)表达情况,实时荧光定量PCR检测小鼠皮质区白细胞介素(interleukin,IL)-1β、IL-6和IL-10 mRNA水平,Western blot法检测小鼠皮质 TREM2、磷酸酰肌醇 3-激酶(phosphoinositide-3 kinase,PI3K)、Akt、GSK3β 和 β-连环蛋白(beta-catenin,β-catenin)的蛋白表达.结果表明,与正常组相比,模型组小鼠逃避潜伏期显著延长,目标象限停留时间和穿越平台次数显著减少(P<0.01),模型组小鼠皮质内神经元数量明显减少,并出现核固缩现象,且Aβ1-42及CD86表达明显增多,组织内IL-1β 和IL-6 mRNA水平显著升高,IL-10 稍有升高,Arg1 则明显下降,皮质区 TREM2、p-PI3K(Y607)、p-Akt(T308)、p-GSK3β(Ser9)和 β-catenin 蛋白表达明显下调;与模型组相比,给药组小鼠逃避潜伏期均明显缩短,穿越平台次数和目标象限停留时间明显增加,小鼠皮质区神经元数量增多、核固缩现象改善,Aβ1-42沉积明显减少,IL-1β和IL-6 mRNA和CD86水平显著下降,而IL-10及Arg1显著上升,各给药组小鼠皮质区TREM2、p-PI3K(Y607)、p-Akt(T308)、p-GSK3β(Ser9)和β-catenin蛋白表达显著上调.综上所述,黄连解毒汤减少Aβ1-42表达和脑内炎症保护神经元,从而改善APP/PS1小鼠的学习记忆能力,可能与TREM2/Akt/GSK3β 信号通路有关.
Effect of Huanglian Jiedu Decoction on TREM2/Akt/GSK3β pathway in cerebral cortex of APP/PS1 transgenic mice
The Chinese medical mechanism of Huanglian Jieduo Decoction on treating Alzheimer's disease(AD)characterized by"toxin damaging brain collateral"is still unclear.This study aims to explore the mechanism of Huanglian Jieduo Decoction on regulating triggering receptor expressed on myeloid cells 2(TREM2)/protein kinase B(Akt)/glycogen synthase kinase 3/3(GSK3β)pathway to improve the cognitive deficit in APP/PS1 transgenic mice.APP/PS1 mice of approximately nine months old were randomly divided into the model group,the low,medium,and high(2.5,5,and 10 g·kg-1)groups of Huanglian Jiedu Decoction,and 0.75 mg·kg-1 donepezil hydrochloride group,and the C57BL/6J mice with the same age were taken as the normal group.After one month of continuous oral administration,a Morris water maze was performed to detect the learning and memory ability of mice.Hematoxylin-eosin(HE)staining was applied to observe the morphology of neuronal cells in the cortical area of mice.Immunofluorescence was used to detect the protein expressions of β-amyloid(Aβ1-42),CD86,and arginase 1(Arg1).The mRNA levels of interleukin(IL)-1/3,IL-6,and IL-10 in the cortex of mice were detected by real-time fluorescence quantitative polymerase chain reaction(RT-qPCR).The protein expressions of TREM2,phosphoinositide-3 kinase(PI3K),Akt,GSK3β,and beta-catenin(β-catenin)in mouse cortex were determined by Western blot.The results indicated that the escape latency of the model group was significantly prolonged,and the residence time in the target quadrant and the number of crossing the platform were significantly reduced compared with the normal group.Mice in the model group had a significantly lower number of neurons in the cortex and showed nuclear pyknosis and a significant increase in the expressions of Aβ1-42 and CD86.The mRNA levels of IL-1β and IL-6 in tissue were significantly increased,IL-10 were increased,while Argl were significantly decreased.The expression of TREM2,p-PI3K(Y607),p-Akt(T308),p-GSK3β(Ser9),and β-catenin in the cortex were significantly down-regulated.Compared with the model group,the escape latency of the mice in the administration group was significantly shortened,and the number of crossing the platform and the residence time in the target quadrant were significantly increased.Furthermore,the number of neurons in the cortex of mice was increased,and nuclear pyknosis was improved.Aβ1-42 deposition was decreased significantly.The mRNA levels of IL-1β,IL-6 and CD86 were significantly decreased,while IL-10 and Arg1 levels were significantly increased.The expression of TREM2,p-PI3K(Y607),p-Akt(T308),p-GSK3β(Ser9),and β-catenin protein in the cortex of each administration group was significantly up-regulated compared with the model group.In conclusion,Huanglian Jiedu Decoction reduced the expression of Aβ1-42 and neuroinflammation to a neuro-protective effect,thereby improving the learning and memory ability in APP/PS1 mice,which may be related to the TREM2/Akt/GSK3β signaling pathway.

Alzheimer's diseaseHuanglian Jiedu DecoctionneuroinflammationTREM2GSK3β

王瑞芳、宋军营、赵焕东、贾亚泉、袁永、丁蕊、王孟菲、张振强

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河南中医药大学中医药科学院,河南郑州 450046

河南中医药大学第一临床医学院,河南郑州 450046

河南中医药大学第二临床医学院,河南郑州 450046

阿尔茨海默病 黄连解毒汤 神经炎症 TREM2 GSK3β

河南省重点研发与推广专项河南省重点研发与推广专项河南省高校科技创新团队支持计划项目河南省自然科学基金面上项目

23210231050521210231108421IRTSTHN026222300420483

2024

中国中药杂志
中国药学会

中国中药杂志

CSTPCD北大核心
影响因子:1.718
ISSN:1001-5302
年,卷(期):2024.49(7)
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