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基于网络药理学、分子模拟及实验验证探讨益脑胶囊治疗阿尔茨海默病的作用机制

余寅丰 王智森 晁桂林 陈君 马东来 马旭伟 梁策

中国中医药信息杂志2026,Vol.33Issue(9):27-37,11.
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中国中医药信息杂志2026,Vol.33Issue(9):27-37,11.DOI:10.19879/j.cnki.1005-5304.202603554

基于网络药理学、分子模拟及实验验证探讨益脑胶囊治疗阿尔茨海默病的作用机制

Exploration on the Mechanism of Yinao Capsules in Alzheimer Disease Based on Network Pharmacology,Molecular Simulation,and Experimental Verification

余寅丰 1王智森 2晁桂林 1陈君 2马东来 3马旭伟 4梁策3

作者信息

  • 1. 河北中医药大学药学院,河北 石家庄 050200
  • 2. 石家庄藏诺药业股份有限公司,河北 石家庄 050035||河北省民族药制剂产业技术研究院,河北 石家庄 050035
  • 3. 河北中医药大学药学院,河北 石家庄 050200||河北省中药组方制剂技术创新中心,河北 石家庄 050091
  • 4. 石家庄东方药业股份有限公司,河北 石家庄 050031
  • 折叠

摘要

Abstract

Objective To investigate the potential mechanism of Yinao Capsules in the treatment of Alzheimer disease(AD)through network pharmacology,molecular simulation,molecular dynamics simulations,and experimental validation.Methods Network pharmacology methods were comprehensively applied to screen active components and potential targets of Yinao Capsules for AD treatment,and a drug-component-target network was constructed.GO and KEGG pathway enrichment analyses were performed on the intersection targets.Molecular docking and molecular dynamics simulations were used to verify binding interactions of core components and targets.Taking C57BL/6 mice as the normal group,APP/PS1 transgenic mice were randomly divided into model group,donepezil hydrochloride group(0.65 mg/kg)and Yinao Capsules low-and high-dosage groups(351 and 1 404 mg/kg),and were intervened for 60 days.Cognitive ability was evaluated using novel object recognition and Morris water maze tests.Hippocampal CA1 neuronal morphology was observed via HE staining.Serum contents of IL-6 and TNF-α were detected by ELISA.Protein expressions of CASP3 and BCL2 in brain tissue were measured by Western blot.Results Network pharmacology identified 66 active components,including deoxyharringtonine and ginsenoside Rg5_qt,and 218 potential targets,with AKT1,IL6,and CASP3 as core targets.The enrichment analysis results of GO and KEGG pathways showed that Yinao Capsules intervened in AD through protein phosphorylation,G protein coupled receptor signal pathway coupled with cyclic nucleotide second messenger,positive regulation of ERK1 and ERK2 cascade reaction and Alzheimer disease,neuroactive ligand receptor interaction,neurodegenerative disease pathway-a variety of diseases,cell apoptosis and other pathways.Molecular docking and dynamics simulations confirmed that β-sitosterol and GSK3B form a stable complex.Animal experiments showed that Yinao Capsules significantly improved cognitive function in mice(P<0.05,P<0.01),reduced serum IL-6 and TNF-α contents(P<0.05),up-regulated BCL2 protein expression and inhibited CASP3 protein activation(P<0.05),and reduced neuronal loss in the hippocampal CA1 region.Conclusion Yinao Capsules can exert synergistic effects through multiple components,regulating key signaling nodes such as AKT1/GSK3β and IL-6/TNF-α,inhibiting neuroinflammation and apoptosis,thereby improving cognitive function and hippocampal pathological damage in AD model mice.Its mechanism involves multiple signaling pathways including AD-related pathways.

关键词

阿尔茨海默病/益脑胶囊/网络药理学/分子对接/APP/PS1小鼠/神经炎症

Key words

Alzheimer disease/Yinao Capsules/network pharmacology/molecular docking/APP/PS1 mice/neuroinflammation

分类

医药卫生

引用本文复制引用

余寅丰,王智森,晁桂林,陈君,马东来,马旭伟,梁策..基于网络药理学、分子模拟及实验验证探讨益脑胶囊治疗阿尔茨海默病的作用机制[J].中国中医药信息杂志,2026,33(9):27-37,11.

基金项目

河北省省级科技计划(25362501D) (25362501D)

河北省中医药管理局科研计划(2021098) (2021098)

河北省高等学校科学研究项目(QN2026454) (QN2026454)

中国中医药信息杂志

1005-5304

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