Network pharmacology and in vivo experiments reveal the pharmacological effects and molecular mechanisms of Simiao Powder in prevention and treatment for gout

被引:12
作者
Xu, Huachong [1 ]
Wu, Jialin [1 ]
Wang, Shiqi [1 ]
Xu, Lu [1 ]
Liu, Pei [1 ]
Shi, Yucong [1 ]
Wu, Sizhi [1 ]
Deng, Li [1 ]
Chen, Xiaoyin [1 ]
机构
[1] Jinan Univ, Coll Tradit Chinese Med, Guangzhou 510632, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Simiao Powder; Gout; Traditional Chinese medicine; Network pharmacology; US GENERAL-POPULATION; SERUM URIC-ACID; ACTIVE INGREDIENTS; RENAL DYSFUNCTION; PPAR-GAMMA; HYPERURICEMIA; INFLAMMATION; PREVALENCE; MANAGEMENT; URATE;
D O I
10.1186/s12906-022-03622-0
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background Gout is a common disease with high incidence due to unhealthy diet and living habits. Simiao Powder, as a classic formula consisted of four common herbs, has been widely used in clinical practice since ancient times to prevent and treat gout. However, the pharmacological mechanism of Simiao Powder is still unclear. Methods Based on network pharmacology, Simiao Powder active compounds were identified in TCMSP, ETCM and BATMAN database, used to establish a network of interaction between potential targets of Simiao Powder and known therapeutic targets of gout. Subsequently, the key potential targets are being used for protein-protein interaction, GO enrichment analysis and KEGG pathway enrichment analysis through several authoritative open databases. Molecular docking through AutoDockTools software can verify interaction between molecules. Finally, to validate the predicted results, in vivo experiments based on hyperuricemic-gout mice model were designed and treated with Simiao powder and allopurinol. Serum levels of uric acid (UA), creatinine (Cr), blood urea nitrogen (BUN) and xanthine oxidase (XOD) were determined using a customized assay kit while the expression of PPAR-gamma, PTGS1, IL-6 and Bcl2 mRNA were analyzed through qRT-PCR. Results Disease-target-compound network was visualized basing on the 20 bioactive compounds and the 19 potential targets using Cytoscape software. The results of PPI analysis, GO enrichment and KEGG pathway enrichment analysis indicate that the potential mechanism of Simiao Powder in treating gout may be achieved by regulating immune and inflammatory reactions, improving metabolism and endocrine. The results of molecular docking show that most of the targets and components have good binding activity. In vivo experiments revealed that Simiao powder can decreased serum UA and XOD levels in hyperuricemic-gout mice, and improved renal function. Furthermore, Simiao powder certainly regulates the expression of PPAR-gamma, PTGS1, IL-6 and Bcl2 mRNA in ankle tissue in hyperuricemic-gout mice. Conclusion Collectively, this research predicted a multiple compounds, targets, and pathways model mechanism of Simiao Powder in the prevention and treatment of gout, providing new ideas and methods for in-depth research, via vivo experiments.
引用
收藏
页数:17
相关论文
共 75 条
  • [1] Al-Okbi Sahar Y., 2014, Asian Pacific Journal of Tropical Biomedicine, V4, P618, DOI 10.12980/APJTB.4.201414B66
  • [2] Leptin might be a regulator of serum uric acid concentrations in humans
    Bedir, A
    Topbas, M
    Tanyeri, F
    Alvur, M
    Arik, N
    [J]. JAPANESE HEART JOURNAL, 2003, 44 (04): : 527 - 536
  • [3] Changes in PTGS1 and ALOX12 Gene Expression in Peripheral Blood Mononuclear Cells Are Associated with Changes in Arachidonic Acid, Oxylipins, and Oxylipin/Fatty Acid Ratios in Response to Omega-3 Fatty Acid Supplementation
    Berthelot, Claire C.
    Kamita, Shizuo George
    Sacchi, Romina
    Yang, Jun
    Nording, Malin L.
    Georgi, Katrin
    Karbowski, Christine Hegedus
    German, J. Bruce
    Weiss, Robert H.
    Hogg, Ronald J.
    Hammock, Bruce D.
    Zivkovic, Angela M.
    [J]. PLOS ONE, 2015, 10 (12):
  • [4] The mechanisms of inflammation in gout and pseudogout (CPP-induced arthritis)
    Busso, N.
    Ea, H. -K.
    [J]. REUMATISMO, 2011, 63 (04) : 230 - 237
  • [5] Peroxisome Proliferator Activated Receptor gamma (PPARγ) Agonist Rosiglitazone Ameliorate Airway Inflammation by Inhibiting Toll-Like Receptor 2 (TLR2)/Nod-Like Receptor with Pyrin Domain Containing 3 (NLRP3) Inflammatory Corpuscle Activation in Asthmatic Mice
    Cheng, Yinzhi
    Li, Shuai
    Wang, Muzi
    Cheng, Cheng
    Liu, Rongyu
    [J]. MEDICAL SCIENCE MONITOR, 2018, 24 : 9045 - 9053
  • [6] Mechanistic Aspects of Inflammation and Clinical Management of Inflammation in Acute Gouty Arthritis
    Cronstein, Bruce N.
    Sunkureddi, Prashanth
    [J]. JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2013, 19 (01) : 19 - 29
  • [7] Gout
    Dalbeth, Nicola
    Merriman, Tony R.
    Stamp, Lisa K.
    [J]. LANCET, 2016, 388 (10055) : 2039 - 2052
  • [8] Mechanism of Action of Colchicine in the Treatment of Gout
    Dalbeth, Nicola
    Lauterio, Thomas J.
    Wolfe, Henry R.
    [J]. CLINICAL THERAPEUTICS, 2014, 36 (10) : 1465 - 1479
  • [9] Cellular Characterization of the Gouty Tophus A Quantitative Analysis
    Dalbeth, Nicola
    Pool, Bregina
    Gamble, Greg D.
    Smith, Timothy
    Callon, Karen E.
    McQueen, Fiona M.
    Cornish, Jillian
    [J]. ARTHRITIS AND RHEUMATISM, 2010, 62 (05): : 1549 - 1556
  • [10] Autophagy inhibition prevents glucocorticoid-increased adiposity via suppressing BAT whitening
    Deng, Jiali
    Guo, Yajie
    Yuan, Feixiang
    Chen, Shanghai
    Yin, Hanrui
    Jiang, Xiaoxue
    Jiao, Fuxin
    Wang, Fenfen
    Ji, Hongbin
    Hu, Guohong
    Ying, Hao
    Chen, Yan
    Zhai, Qiwei
    Xiao, Fei
    Guo, Feifan
    [J]. AUTOPHAGY, 2020, 16 (03) : 451 - 465