A Network Pharmacology to Explore the Mechanism of Membranaceus in the Treatment of Diabetic Retinopathy.

Evid Based Complement Alternat Med

Surgical Department of Fundus Disease and Trauma, Eye Hospital, China Academy of Chinese Medical Sciences, Beijing 100040, China.

Published: November 2020

AI Article Synopsis

  • Diabetic retinopathy (DR) is caused by retinal damage from diabetes, severely affecting vision and quality of life, making it a significant burden on individuals and society.
  • Recent studies suggest that Membranaceus (AM), a traditional Chinese medicine, may have potential in treating DR, although its exact mechanism remains unclear.
  • This research identifies 24 active compounds from AM and 38 core targets linked to its therapeutic effects on DR, indicating AM works through various pathways involved in oxidative stress, cell apoptosis, and inflammation.

Article Abstract

Background: Diabetic retinopathy (DR) includes a series of typical lesions affected by retinal microvascular damage caused by diabetes mellitus (DM), which not only seriously damages the vision, affecting the life's quality of patients, but also brings a considerable burden to the family and society. Membranaceus (AM) is a commonly used medicine in clinical therapy of eye disorders in traditional Chinese medicine (TCM). In recent years, it is also used for treating DR, but the specific mechanism is unclear. Therefore, this study explores the potential mechanism of AM in DR treatment by using network pharmacology.

Methods: Based on the oral bioavailability (OB) and drug likeness (DL) of two ADME (absorption, distribution, metabolism, excretion) parameters, Traditional Chinese Medicine Systems Pharmacology Database (TCMSP), Swiss Target Prediction platform, GeneCards, and OMIM database were used to predict and screen the active compounds of AM, the core targets of AM in DR treatment. The Metascape data platform was used to perform Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis on the core targets.

Results: 24 active compounds were obtained, such as quercetin, kaempferol, and astragaloside IV. There were 169 effective targets of AM in DR treatment, and the targets were further screened and finally, 38 core targets were obtained, such as VEGFA, AKT1, and IL-6. EGFR tyrosine kinase inhibitor resistance, AGE-RAGE signaling pathway in diabetic complications, PI3K-Akt signaling pathway, and other metabolic pathways participated in oxidative stress, cell apoptosis, angiogenesis signal transduction, inflammation, and other biological processes.

Conclusion: AM treats DR through multiple compounds, multiple targets, and multiple pathways. AM may play a role in the treatment of DR by targeting VEGFA, AKT1, and IL-6 and participating in oxidative stress, angiogenesis, and inflammation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652614PMC
http://dx.doi.org/10.1155/2020/8878569DOI Listing

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