Anti-Respiratory Syncytial Virus Mechanism of Houttuynia cordata Thunb Exploration based on Network Pharmacology

Author:

Du Haitao1,Ding Jie1,Wang Ping2,Zhang Guisheng3,WANG Dandan4,Ma Qingyun1,Li Na1,Sun Tiefeng5

Affiliation:

1. School of Pharmaceutical Sciences, Shandong University of Traditional Chinese Medicine, Jinan 250355, P.R. , China

2. State Key Laboratory of Precision Measurement Technology and Instruments, Tianjin University, Tianjin 300072, P.R. , China

3. College of Science and Technology, Shandong University of Traditional Chinese Medicine, Jinan 250355, China

4. Bone Biomechanics Engineering Laboratory of Shandong Province, Neck-Shoulder and Lumbocrural Pain Hospital, Shandong Medicinal Biotechnology Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250062, China

5. Shandong Academy of Chinese Medicine, Jinan 250014, P.R, China

Abstract

Background and Objective: : Respiratory Syncytial Virus (RSV) is the leading cause of infant lower respiratory tract infections with no mature vaccines and medicines available. Pneumonia caused by RSV kills many infants every year. There are unique advantages for Traditional Chinese Medicine (TCM) to fight against the virus. Houttuynia cordata Thunb is a commonly used anti-virus medicine in TCM, but its mechanism has not been investigated. The current study explores the anti-RSV mechanism of H. cordata Thunb by means of network pharmacology and bioinformatics. Method: The candidate compounds of H. cordata Thunb and the potential targets were obtained from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP), PubMed, CNKI, PubChem Database, and Swiss Target Prediction database. Then the potential targets and pathways of H. cordata Thunb against RSV were screened by GeneCards, GenCLiP 3, and NCBI Database. We developed a Protein-Protein Interactions (PPI) Network and Compound-Target-Pathway Network through the Cytoscape software. Furthermore, core targets were preliminary verification by Gene Expression Omnibus (GEO) database by bioinformatics methods. At last, the first 6 pathways were screened out to draw a map of the main target signal pathways. Results:: A total of 12 potentially active compounds and 47 potential interaction targets were screened. PPI Network and data from GEO showed that IL-6, STAT3, TNF, AKT1, PTGS2, SRC, and MAPK3 may play a core role in the antivirus process. KEGG enrichment pathway analysis predicted that H. cordata Thunb exerted its anti-RSV effect by regulating TNF, Rap1, HIF-1, PI3K-Akt, MAPK, and VEGF signaling pathways. Conclusion: : This study preliminarily predicted the main active compounds, targets and related pathways of H. cordata Thunb in the treatment of RSV-induced diseases, which laid a good foundation for further revealing its mechanism.

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry,Computer Science Applications,Drug Discovery,General Medicine

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