Exploring the Pharmacological Mechanism of Liuwei Dihuang Decoction for Diabetic Retinopathy: A Systematic Biological Strategy-Based Research
Author(s) -
Mengxia Yuan,
Qi He,
Zhiyong Long,
Xiaofei Zhu,
Wang Xiang,
Yonghe Wu,
Shibin Lin
Publication year - 2021
Publication title -
evidence-based complementary and alternative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.552
H-Index - 90
eISSN - 1741-4288
pISSN - 1741-427X
DOI - 10.1155/2021/5544518
Subject(s) - diabetic retinopathy , angiogenesis , signal transduction , mechanism (biology) , gene ontology , pharmacology , medicine , diabetes mellitus , bioinformatics , biology , gene , cancer research , gene expression , endocrinology , microbiology and biotechnology , biochemistry , philosophy , epistemology
Objective To explore the pharmacological mechanism of Liuwei Dihuang decoction (LDD) for diabetic retinopathy (DR).Methods The potential targets of LDD were predicted by PharmMapper. GeneCards and other databases were used to collect DR genes. Cytoscape was used to construct and analyze network DR and LDD's network, and DAVID was used for Gene Ontology (GO) and pathway enrichment analysis. Finally, animal experiments were carried out to verify the results of systematic pharmacology.Results Five networks were constructed and analyzed: (1) diabetic retinopathy genes' PPI network; (2) compound-compound target network of LDD; (3) LDD-DR PPI network; (4) compound-known target network of LDD; (5) LDD known target-DR PPI network. Several DR and treatment-related targets, clusters, signaling pathways, and biological processes were found. Animal experiments found that LDD can improve the histopathological changes of the retina. LDD can also increase erythrocyte filtration rate and decrease the platelet adhesion rate ( P < 0.05) and decrease MDA and TXB2 ( P < 0.05). Compared with the model group, the retinal VEGF and HIF-1 α expression in the LDD group decreased significantly ( P < 0.05).Conclusion The therapeutic effect of LDD on DR may be achieved by interfering with the biological processes (such as response to insulin, glucose homeostasis, and regulation of angiogenesis) and signaling pathways (such as insulin, VEGF, HIF-1, and ErbB signaling pathway) related to the development of DR that was found in this research.
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