» Articles » PMID: 35172688

Mechanism of Action of for Treatment of Idiopathic Membranous Nephropathy Based on Network Pharmacology

Overview
Journal Ren Fail
Publisher Informa Healthcare
Date 2022 Feb 17
PMID 35172688
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Although thunder god vine () has been widely used for treatment of idiopathic membranous nephropathy (IMN), the pharmacological mechanisms underlying its effects are still unclear. This study investigated potential therapeutic targets and the pharmacological mechanism of for the treatment of IMN based on network pharmacology.

Methods: Active components of were obtained from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform. IMN-associated target genes were collected from the GeneCards, DisGeNET, and OMIM databases. VENNY 2.1 was used to identify the overlapping genes between active compounds of and IMN target genes. The STRING database and Cytoscape 3.7.2 software were used to analyze interactions among overlapping genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses of the targets were performed using Rx64 4.0.2 software, colorspace, stringi, DOSE, clusterProfiler, and enrichplot packages.

Results: A total of 153 compound-related genes and 1485 IMN-related genes were obtained, and 45 core genes that overlapped between both categories were identified. The protein-protein interaction network and MCODE results indicated that the targets TP53, MAPK8, MAPK14, STAT3, IFNG, ICAM1, IL4, TGFB1, PPARG, and MMP1 play important roles in the treatment of on IMN. Enrichment analysis showed that the main pathways of targets were the AGE signaling pathway, IL-17 signaling pathway, TNF signaling pathway, and Toll-like receptor signaling pathway.

Conclusion: This study revealed potential multi-component and multi-target mechanisms of for the treatment of IMN based on network pharmacological, and provided a scientific basis for further experimental studies.

Citing Articles

IgG4-related disease complicated by PLA2R-associated membranous nephropathy: A case report.

Huang M, Liu J, Li X Open Life Sci. 2024; 19(1):20220921.

PMID: 39071497 PMC: 11282913. DOI: 10.1515/biol-2022-0921.


Effectiveness and safety of tripterygium wilfordii poly-glycosides on glomerulonephritis: a systematic review and meta-analysis.

Yan X, Shi J, Zhang Y, Liu J, Lin X, Yu C Front Pharmacol. 2024; 15:1339153.

PMID: 38841368 PMC: 11150713. DOI: 10.3389/fphar.2024.1339153.


QiDiTangShen granules alleviates diabetic nephropathy podocyte injury: A network pharmacology study and experimental validation in vivo and vitro.

Gao F, Zhou Y, Yu B, Xie H, Shi Y, Zhang X Heliyon. 2024; 10(1):e23535.

PMID: 38223704 PMC: 10784173. DOI: 10.1016/j.heliyon.2023.e23535.


Membranous nephropathy: Systems biology-based novel mechanism and traditional Chinese medicine therapy.

Miao H, Zhang Y, Yu X, Zou L, Zhao Y Front Pharmacol. 2022; 13:969930.

PMID: 36176440 PMC: 9513429. DOI: 10.3389/fphar.2022.969930.

References
1.
Polanco N, Gutierrez E, Rivera F, Castellanos I, Baltar J, Lorenzo D . Spontaneous remission of nephrotic syndrome in membranous nephropathy with chronic renal impairment. Nephrol Dial Transplant. 2011; 27(1):231-4. DOI: 10.1093/ndt/gfr285. View

2.
Meng S, Sun L, Wang L, Lin Z, Liu Z, Xi L . Loading of water-insoluble celastrol into niosome hydrogels for improved topical permeation and anti-psoriasis activity. Colloids Surf B Biointerfaces. 2019; 182:110352. DOI: 10.1016/j.colsurfb.2019.110352. View

3.
Malik S, Bhatia J, Suchal K, Gamad N, Dinda A, Gupta Y . Nobiletin ameliorates cisplatin-induced acute kidney injury due to its anti-oxidant, anti-inflammatory and anti-apoptotic effects. Exp Toxicol Pathol. 2015; 67(7-8):427-33. DOI: 10.1016/j.etp.2015.04.008. View

4.
Huang Y, Fu S, Lu K, Chen J, Hsieh H, Sytwu H . Inhibition of tumor necrosis factor signaling attenuates renal immune cell infiltration in experimental membranous nephropathy. Oncotarget. 2018; 8(67):111631-111641. PMC: 5762348. DOI: 10.18632/oncotarget.22881. View

5.
Sharma D, Gondaliya P, Tiwari V, Kalia K . Kaempferol attenuates diabetic nephropathy by inhibiting RhoA/Rho-kinase mediated inflammatory signalling. Biomed Pharmacother. 2018; 109:1610-1619. DOI: 10.1016/j.biopha.2018.10.195. View