Screening of traditional Chinese medicine-derived snail control drug targets based on network pharmacology
10.16250/j.32.1374.2022126
- VernacularTitle:基于网络药理学的中药来源灭螺药物相关靶点筛选
- Author:
Tao XIONG
1
;
Jin-lu GUO
2
;
Fang-guo LU
1
;
Jia-hao LIU
2
;
Tao ZHENG
2
;
Jia-shan LI
2
Author Information
1. Department of Microbiology, School of Medicine, Hunan University of Chinese Medicine, Changsha, Hunan 410219, China
2. School of Stomatology, Hunan University of Chinese Medicine, China
- Publication Type:Journal Article
- Keywords:
Oncomelania hupensis;
Pomacea;
Molluscicide;
Traditional Chinese medicine;
Network pharmacology
- From:
Chinese Journal of Schistosomiasis Control
2022;34(6):588-597
- CountryChina
- Language:Chinese
-
Abstract:
Objective To screen the targets of traditional Chinese medicine-derived potential plant molluscicides based on network pharmacology and explore the mechanisms of molluscicidal actions. Methods The traditional Chinese medicines with molluscicidal actions were screened based on retrospective literature reviews, and their molluscicidal efficiency was summarized. The active ingredients and potential targets of traditional Chinese medicines were captured from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform, Unified Protein Database and literature mining using network pharmacology. The drug-active ingredient-target network was created using the software Cytoscape 3.7.2, and the key targets were subjected to Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis using the Metascape software. Results A total of 27 types of snail control drugs derived from traditional Chinese medicines were screened from publications and classified into 14 categories. Network pharmacology identified 190 active ingredients, and the active ingredients with a high degree in the drug-active ingredient-target network included quercetin, linoleyl acetate, luteolin, beta-carotene, (24S)-ethylcholesta-5,22,25-trans-3beta-ol, fumarine and arctiin, with 181 corresponding potential targets screened. KEGG pathway enrichment analysis revealed that these targets were mainly located in 16 pathways, including the neuroactive ligand-receptor interactions, regulation of adipocyte lipolysis and adrenergic signal in myocardial cells. Conclusions This study preliminarily demonstrates the multi-ingredient, multi-target and multi-pathway mechanisms of action of 27 molluscicides. The screened key ingredient may provide the basis for isolation, purification and pharmacological studies of molluscicides, and the screened key targets and key pathways may facilitate the illustration of mechanisms of actions of traditional Chinese medicine-derived molluscicides and development of novel green molluscicides.
