Exploration of the main active components and pharmacological mechanism of Yerba Mate based on network pharmacology

被引:1
作者
Yue, Zhaodi [1 ,2 ,5 ,6 ,7 ]
Fu, Hui [8 ]
Ma, Huifen [4 ]
Li, Li [1 ,2 ]
Feng, Ziyun [1 ,2 ]
Yin, Yanyan [1 ,2 ,5 ,7 ]
Wang, Fangqi [7 ]
Du, Bingyu [1 ,2 ,5 ,6 ,7 ]
Liu, Yibo [1 ,2 ,5 ,6 ,7 ]
Zhao, Renjie [1 ,2 ,5 ,6 ,7 ]
Kan, Mengfan [1 ,2 ,5 ,6 ,7 ]
Sun, Helin [1 ,2 ,5 ,6 ]
Zhang, Zhongwen [1 ,2 ,5 ,6 ]
Yu, Shaohong [1 ,2 ,3 ]
机构
[1] Shandong Med Univ 1, Affiliated Hosp 1,, Shandong Univ Tradit Chinese Med 2, Affiliated Hosp 2,Shandong Univ Tradit Chinese Med, Jinan, Peoples R China
[2] Shandong Prov Qianfoshan Hosp, Jinan, Peoples R China
[3] Shandong Univ Tradit Chinese Med, Clin Med Coll 2, Jinan, Peoples R China
[4] Natl Hlth Commiss Capac Bldg, Continuing Educ Ctr, Beijing, Peoples R China
[5] Shandong Med Univ 1, Affiliated Hosp 1, Dept Endocrinol & Metabol, Jinan, Peoples R China
[6] Shandong Prov Qianfoshan Hosp, Shandong Inst Nephrol, Shandong Key Lab Rheumat Dis & Translat Med, Jinan, Peoples R China
[7] Shandong Univ Tradit Chinese Med, Coll Rehabil Med, Jinan, Peoples R China
[8] Shandong Univ, Cheeloo Coll Med, Jinan, Peoples R China
关键词
yerba mate; pharmacological mechanism; biotargets; network pharmacology; ILEX-PARAGUARIENSIS; LUNG-CANCER; METABOLISM; MICE;
D O I
10.5603/EP.a2022.0026
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Yerba mate is widely consumed in South American countries and is gaining popularity around the world. Long-term consumption of yerba mate has been proven to have health-care functions and therapeutic effects on many diseases; however, its underlying mechanism has not been clearly elucidated. In this research, we explored the pharmacological mechanism of yerba mate through a network pharmacological approach.Material and metbods: The bioactive components of yerba mate were screened from published literature and the Traditional Chinese Medicine System Pharmacology Database (TCMSP), and the targets and related diseases were retrieved by TCMSP. Furthermore, the component-target-disease network and protein-protein interaction (PPI) network were constructed, and combined with gene ontology (GO) functional analysis and Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway enrichment analysis to explore the pharmacological mechanism of yerba mate.Results: As a result, 16 bioactive components of yerba mate were identified, which acted on 229 targets in total. Yerba mate can be used to treat 305 diseases, such as breast cancer, asthma, Alzheimer's disease, osteoarthritis, diabetes mellitus, atherosclerosis, and obesity. Protein kinase B (AKT1), signal transducer and activator of transcription 3 (STAT3), mitogen-activated protein kinase 1 (MAPK1), transcription factor AP-1 (JUN), cellular tumour antigen (p53) TP53, tumour necrosis factor (TNF), transcription factor p65 (RELA), interleukin-6 (IL6), amyloid-beta precursor protein (APP), and vascular endothelial growth factor A (VEGFA) were identified as the key targets of yerba mate playing pharmacological roles. The signalling pathways identified by KEGG pathway enrichment analysis that were most closely related to the effects of yerba mate included pathways in cancer, fluid shear stress and atherosclerosis, and human cytomegalovirus infection. Conclusion: The results of our study preliminarily verify the basic pharmacological action and possible mechanism of yerba mate and provide a reference for the further development of its medicinal value. (Endokrynol Pol 2022; 73 (4): 725-735)
引用
收藏
页码:725 / 735
页数:11
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