Network pharmacology, molecular docking, and animal experiments reveal mechanism of Zhizhu Decoction in regulating macrophage polarization to reduce adipose tissue inflammation in obese children.
10.19540/j.cnki.cjcmm.20241009.502
- Author:
Yong-Kai YIN
1
;
Chang-Miao NIU
2
;
Li-Ting LIANG
2
;
Mo DAN
1
;
Tian-Qi GAO
1
;
Yan-Hong QIN
2
;
Xiao-Ning YAN
1
Author Information
1. the Third Clinical Medical College of Shanxi University of Chinese Medicine,Shanxi Provincial Integrated TCM and WM Hospital Jinzhong 030619, China.
2. the First Clinical Medical College of Shanxi University of Chinese Medicine Jinzhong 030619, China.
- Publication Type:Journal Article
- Keywords:
Zhizhu Decoction;
adipose tissue inflammation;
macrophages;
network pharmacology;
obese children
- MeSH:
Animals;
Drugs, Chinese Herbal/pharmacology*;
Molecular Docking Simulation;
Adipose Tissue/immunology*;
Mice;
Male;
Humans;
Network Pharmacology;
Macrophages/immunology*;
Mice, Inbred C57BL;
Child;
Protein Interaction Maps/drug effects*;
Obesity/genetics*;
Inflammation/drug therapy*
- From:
China Journal of Chinese Materia Medica
2025;50(1):228-238
- CountryChina
- Language:Chinese
-
Abstract:
Network pharmacology and molecular docking were employed to predict the mechanism of Zhizhu Decoction in regulating macrophage polarization to reduce adipose tissue inflammation in obese children, and animal experiments were then carried out to validate the prediction results. The active ingredients and targets of Zhizhu Decoction were retrieved from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform(TCMSP). The inflammation related targets in the adipose tissue of obese children were searched against GeneCards, OMIM, and DisGeNET, and a drug-disease-target network was established. STRING was used to construct a protein-protein interaction(PPI) network and screen for core targets. R language was used to carry out Gene Ontology(GO) and Kyoto Encyclopedia of Genes and Genomes(KEGG) pathway enrichment analyses. AutoDock was used for the molecular docking between core targets and active ingredients. 24 SPF grade 6-week C57B/6J male mice were adaptively fed for 1 week, and 8 mice were randomly selected as the blank group. The remaining 16 mice were fed with high-fat diet for 8 weeks to onstruct a high-fat diet induced mouse obesity model. After successful modeling, the 16 mice were randomly divided into model group and Zhizhu Decoction group, with 8 mice in each group. Zhizhu Decoction group was intervened by gavage for 14 days, once a day. Blank group and model group were given an equal amount of sterile double distilled water(ddH_2O) by gavage daily. After the last gavage, serum and inguinal adipose tissue were collected from mice for testing. The morphology of inguinal adipose tissue was observed by hematoxylin-eosin(HE) staining, the levels of inflammatory factors interleukin-6(IL-6) and tumor necrosis factor-α(TNF-α)were detected by enzyme-linked immunosorbent assay(ELISA), and the protein expression of macrophage marker molecule nitric oxide synthase(iNOS) and epidermal growth factor like hormone receptor 1(F4/80) was detected by immunofluorescence staining. Network pharmacology predicted luteolin, naringenin, and nobiletin as the main active ingredients in Zhizhu Decoction and 15 core targets. KEGG pathway enrichment analysis revealed involvement in the key signaling pathway of nuclear factor κB(NF-κB). Molecular docking showed that the active ingredients of Zhizhu Decoction bound well to the core targets. Animal experiment showed that compared with the model group, Zhizhu Decoction reduced the distribution of inflammatory cytokines in the inguinal adipose tissue of mice, lowered the levels of TNF-α and IL-6 in the serum(P<0.05, P<0.01), and down-regulated the expression of iNOS and F4/80(P<0.05). The results showed that the active ingredients in Zhizhu Decoction, such as luteolin, naringenin, and nobiletin, inhibit the aggregation of macrophages in adipose tissue, downregulate their classic activated macrophage(M1) polarization, reduce the expression of inflammatory factors IL-6 and TNF-α, and thus improve adipose tissue inflammation in obese mice.
