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基于网络药理学与分子对接及生物信息学的全杜仲胶囊抗高血压肾病作用机制

毛金娣 周朝忠 梁兆昌 王素芸 艾文强 刘厚权 唐云

井冈山大学学报(自然科学版)2026,Vol.47Issue(3):42-49,8.
井冈山大学学报(自然科学版)2026,Vol.47Issue(3):42-49,8.DOI:10.3969/j.issn.1674-8085.2026.03.006

基于网络药理学与分子对接及生物信息学的全杜仲胶囊抗高血压肾病作用机制

Action mechanism of Quanduzhong capsule against anti-hypertensive nephropathy based on network pharmacology,molecular docking and bioinformatics

毛金娣 1周朝忠 1梁兆昌 2王素芸 3艾文强 3刘厚权 3唐云2

作者信息

  • 1. 井冈山大学中医药学院,江西,吉安 343009||江西普正制药股份有限公司,江西,吉安 343100
  • 2. 井冈山大学中医药学院,江西,吉安 343009
  • 3. 江西普正制药股份有限公司,江西,吉安 343100
  • 折叠

摘要

Abstract

In this study,network pharmacology,molecular docking and bioinformatics methods were used to systematically elucidate the"multi-component-multi-target and multi-pathway"mechanism underlying the intervention of Quanduzhong capsule in hypertensive nephropathy.Based on the TCMSP and BATMAN-TCM databases,oral bioavailability(OB≥30%)and drug-like properties(DL≥0.18)were defined as screening criteria,and finally 22 key active compounds derived from Eucommia ulmoides were screened.Integrating the SwissTargetPrediction platform,213 potential targets were predicted;a total of 3,025 targets related to hypertensive nephropathy were retrieved from disease databases such as GenCards and DisGeNET.A total of 127"component-disease"intersection targets were obtained by STRING database,which were subsequently imported into Cytoscape to construct a PPI network.With the screening threshold set at a degree value>35,the top 10 core targets such as AKT1,MAPK1,IL6 and VEGFA were identified.GO functional enrichment analysis yielded 2,642 terms,while KEGG enrichment analysis generated 176 entries,and they significantly affected the PI3K-Akt,AGE-RAGE,and HIF-1 signaling pathways.In addition,bioinformatics and molecular docking experiments confirmed that there were differences in the expression of MAPK1,AKT1,and TP53 genes,and these core genes exhibited strong binding affinity to the active component quercetin.In summary,the present study elucidates that Quanduzhong capsule exerts a therapeutic effect against hypertensive nephropathy by regulating the expression of MAPK1,AKT1 and TP53 genes,as well as inhibiting renal cell apoptosis.Its underlying mechanism is predicted to involve the modulation of PI3K-AKT signaling pathway,which provides novel scientific evidence for the prevention and treatment of secondary renal injury with traditional Chinese medicine formulas.

关键词

网络药理学/分子对接/生物信息学/全杜仲胶囊/高血压肾病

Key words

network pharmacology/molecular docking/bioinformatics/Quanduzhong capsule/hypertensive nephropathy

分类

农业科技

引用本文复制引用

毛金娣,周朝忠,梁兆昌,王素芸,艾文强,刘厚权,唐云..基于网络药理学与分子对接及生物信息学的全杜仲胶囊抗高血压肾病作用机制[J].井冈山大学学报(自然科学版),2026,47(3):42-49,8.

基金项目

江西省自然科学基金一般项目(20232BAB206160) (20232BAB206160)

井冈山大学学报(自然科学版)

1674-8085

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