A Network Pharmacological Approach to Explore the Mechanisms of TongXieYaoFang in Inflammatory Bowel Disease

Authors

  • Wenli You Department of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China
  • Mingjuan Li Department of Anesthesiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China
  • Aiting Di Department of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China
  • Xin Li Department of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China
  • Hairui Gao Department of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China
  • Cuixia Qiao Department of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China
  • Bin Yu Department of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China
  • Gang Zhao Department of Anorectal, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China https://orcid.org/0000-0003-3395-4954

DOI:

https://doi.org/10.1590/s2175-97902022e201157

Keywords:

Inflammatory bowel disease, Traditional chinese medicine, TongXieYaoFang, BaiZhuShaoYaoSan, Pharmacological actions

Abstract

Inflammatory bowel disease (IBD) is a chronic inflammatory disorder of the intestine, demonstrating an increasing incidence every year. TongXieYaoFang (TXYF) has been used widely in China as a complementary therapy to relieve the symptoms of IBD for hundreds of years. In the present research, a network pharmacology-based approach was used to systematically explore the intrinsic mechanisms of TXYF in IBD at the molecular level. Network pharmacology-based methods, which mainly included database mining, screening of bioactive compounds, target prediction, collection of IBD-related targets, gene enrichment analysis, network construction, and molecular docking, were employed in the present study. Network analysis revealed a total of 108 potential targets derived from 22 component compounds of TXYF, among which 34 targets were common with the IBD-related targets. In the protein-protein interaction (PPI) network, 10 key targets were identified. The gene enrichment analysis suggested that anti-inflammatory processes, such as NF-kappa B signaling pathway and Toll-like receptor signaling pathway, could be the core processes involved in the action of TXYF in IBD. Molecular docking results revealed that three compounds present in TXYF exhibited strong binding affinity for PTGS2. The present study provides novel insights into the molecular mechanisms and network approaches of TXYF action in IBD from a systemic perspective. The potential targets and pathways identified in the present study would assist in further research on the clinical application of TXYF in IBD therapy.

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Published

2022-12-23

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Original Article

How to Cite

A Network Pharmacological Approach to Explore the Mechanisms of TongXieYaoFang in Inflammatory Bowel Disease. (2022). Brazilian Journal of Pharmaceutical Sciences, 58. https://doi.org/10.1590/s2175-97902022e201157