Network Pharmacology Identifies the Mechanisms of Action of TaohongSiwu Decoction Against Essential Hypertension

被引:32
作者
Liu, Tian-hao [1 ]
Chen, Wei-hao [1 ]
Chen, Xu-dong [1 ]
Liang, Qiu-er [1 ]
Tao, Wen-cong [1 ]
Lin, Zhen [1 ]
Xiao, Ya [1 ]
Chen, Li-guo [1 ]
机构
[1] Jinan Univ, Chinese Med Coll, Guangzhou, Guangdong, Peoples R China
来源
MEDICAL SCIENCE MONITOR | 2020年 / 26卷
关键词
Computer Communication Networks; Hypertension; Phenylephrine; ARTERIAL-HYPERTENSION; SIGNALING PATHWAY; QUERCETIN; EXTRACT; DYSLIPIDEMIA; PREDICTION; FORMULAS; PROTECTS; TARGETS; INJURY;
D O I
10.12659/MSM.920682
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: TaohongSiwu decoction (THSWT), a traditional herbal formula, has been used to treat cardiovascular and cere-brovascular diseases such as essential hypertension (EH) in China. However, the pharmacological mechanism is not clear. To investigate the mechanisms of THSWT in the treatment of EH, we performed compounds, targets prediction and network analysis using a network pharmacology method. Material/Methods: We selected chemical constituents and targets of THSWT according to TCMSP and UniProtKB databases and collected therapeutic targets on EH from Online Mendelian Inheritance in Man (OMIM), Drugbank and DisGeNET databases. The protein-protein interaction (PPI) was analyzed by using String database. Then network was constructed by using Cytoscape_v3.7.1, and the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment was performed by using Database for Annotation, Visualization and Integrated Discovery (DAVID) software. Results: The results of our network pharmacology research showed that the THSWT, composed of 6 Chinese herbs, con- tained 15 compounds, and 23 genes regulated the main signaling pathways related to EH. Moreover, the PPI network based on targets of THSWT on EH revealed the interaction relationship between targets. These core compounds were 6 of the 15 disease-related compounds in the network, kaempferol, quercetin, luteolin, Myricanone, beta-sitosterol, baicalein, and the core genes contained ADRB2, CALM1, HMOX1, JUN, PPARG, and VEGFA, which were regulated by more than 3 compounds and significantly associated with Calcium signaling pathway, cGMP-PKG signaling pathway, cAMP signaling pathway, PI3K-Akt signaling pathway, Rapl signaling pathway, and Ras signaling pathway. Conclusions: This network pharmacological study can reveal potential mechanisms of multi-target and multi-component THSWT in the treatment of EH, provide a scientific basis for studying the mechanism.
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页数:10
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共 54 条
  • [1] Aalbers J, 2010, Cardiovasc J Afr, V21, P120
  • [2] Dipeptidyl Peptidase 4 Inhibition Alleviates Shortage of Circulating Glucagon-Like Peptide-1 in Heart Failure and Mitigates Myocardial Remodeling and Apoptosis via the Exchange Protein Directly Activated by Cyclic AMP 1/Ras-Related Protein 1 Axis
    Aoyama, Morihiko
    Kawase, Haruya
    Bando, Yasuko K.
    Monji, Akio
    Murohara, Toyoaki
    [J]. CIRCULATION-HEART FAILURE, 2016, 9 (01)
  • [3] THE INOSITOL TRISPHOSPHATE/CALCIUM SIGNALING PATHWAY IN HEALTH AND DISEASE
    Berridge, Michael J.
    [J]. PHYSIOLOGICAL REVIEWS, 2016, 96 (04) : 1261 - 1296
  • [4] VEGF/PKD-1 signaling mediates arteriogenic gene expression and angiogenic responses in reversible human microvascular endothelial cells with extended lifespan
    Best, Brad
    Moran, Patrick
    Ren, Bin
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2018, 446 (1-2) : 199 - 207
  • [5] The UniProtKB guide to the human proteome
    Breuza, Lionel
    Poux, Sylvain
    Estreicher, Anne
    Famiglietti, Maria Livia
    Magrane, Michele
    Tognolli, Michael
    Bridge, Alan
    Baratin, Delphine
    Redaschi, Nicole
    Xenarios, Ioannis
    Bougueleret, Lydie
    Bairoch, Amos
    Aimo, Lucila
    Auchincloss, Andrea
    Axelsen, Kristian
    Argoud-Puy, Ghislaine
    Bansal, Parit
    Binz, Pierre-Alain
    Blatter, Marie-Claude
    Boeckmann, Brigitte
    Bolleman, Jerven
    Boutet, Emmanuel
    Braconi-Quintaje, Silvia
    Casal-Casas, Cristina
    de Castro, Edouard
    Cerutti, Lorenzo
    Coudert, Elisabeth
    Cuche, Beatrice
    Cusin, Isabelle
    Doche, Mikael
    Dornevil, Dolnide
    Duvaud, Severine
    Ferro-Rojas, Serenella
    Feuermann, Marc
    Gasteiger, Elisabeth
    Gehant, Sebastien
    Gerritsen, Vivienne
    Gos, Arnaud
    Gruaz-Gumowski, Nadine
    Hinz, Ursula
    Hulo, Chantal
    James, Janet
    Jimenez, Silvia
    Jungo, Florence
    Keller, Guillaume
    Kerhornou, Arnaud
    Kappler, Thomas
    Lane, Lydie
    Lara, Vicente
    Lemercier, Philippe
    [J]. DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION, 2016,
  • [6] Protective effect of luteolin on skin ischemia-reperfusion injury through an AKT-dependent mechanism
    Chen, Gang
    Shen, Hugang
    Zang, Linlin
    Su, Zhonglan
    Huang, Jilong
    Sun, Yong
    Wang, Hongwei
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2018, 42 (06) : 3073 - 3082
  • [7] A Network Pharmacology Approach to Uncover the Mechanisms of Shen-Qi-Di-Huang Decoction against Diabetic Nephropathy
    Di, Sha
    Han, Lin
    Wang, Qing
    Liu, Xinkui
    Yang, Yingying
    Li, Fan
    Zhao, Linhua
    Tong, Xiaolin
    [J]. EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2018, 2018
  • [8] ADRB2 polymorphisms and dyslipidemia risk in Chinese hypertensive patients
    Gu, Wei
    Liu, Jilin
    Wang, Zuoguang
    Liu, Ya
    Wen, Shaojun
    [J]. CLINICAL AND EXPERIMENTAL HYPERTENSION, 2017, 39 (02) : 139 - 144
  • [9] Farnesyl pyrophosphate synthase inhibitor, ibandronate, improves endothelial function in spontaneously hypertensive rats
    Han, Jie
    Jiang, Dong-Mei
    Ye, Yang
    Du, Chang-Qing
    Yang, Jian
    Hu, Shen-Jiang
    [J]. MOLECULAR MEDICINE REPORTS, 2016, 13 (05) : 3787 - 3796
  • [10] The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®
    Hartley, Taila
    Balci, Tugce B.
    Rojas, Samantha K.
    Eaton, Alison
    Dyment, David A.
    Boycott, Kym M.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2018, 178 (04) : 458 - 463