Network Pharmacology-Based Analysis of the Underlying Mechanism of Huajiao for Pain Relief

Mingquan Wu; Hong-Ling Du; Xu Zhou; Wei Peng; Limei Liu; Zhong Zhang; He Tu

doi:10.1155/2021/5526132

Network Pharmacology-Based Analysis of the Underlying Mechanism of Huajiao for Pain Relief

Evid Based Complement Alternat Med. 2021 Apr 4:2021:5526132. doi: 10.1155/2021/5526132. eCollection 2021.

Authors

Mingquan Wu¹, Hong-Ling Du², Xu Zhou¹, Wei Peng¹, Limei Liu¹, Zhong Zhang¹, He Tu^{1

2}

Affiliations

¹ Department of Pharmacy, Sichuan Orthopedic Hospital, Chengdu, Sichuan, China.
² College of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.

Abstract

Objective: Pain is a common symptom among patients, and pain management is an important clinical practice topic. The mechanism of Huajiao (HJ; Zanthoxylum bungeanum Maxim.) and its effective components for treating pain was explored using network pharmacology and molecular docking to verify its pain relief function in traditional medical practice.

Methods: HJ's components were collected via the Traditional Chinese Medicine Systems Pharmacology platform and published studies. HJ-associated target proteins were predicted using the drug similarity rule via Swiss Target Prediction. Online Mendelian Inheritance in Man was used to search for pain-related genes and proteins, and the Database of Interacting Proteins was used to obtain the human interactive target proteins. The compound-target-disease network of HJ for pain relief was constructed with protein-protein interaction networks. The obtained target proteins were uploaded on the Database for Annotation, Visualization, and Integrated Discovery to annotate, visualize, and integrally discover the related signaling pathway, and semiflexible molecular docking by Autodock Vina was applied to verify the potential mechanism.

Results: A total of 157 molecules in HJ were obtained, and the top 20 active components or active groups were mainly focused on the amide alkaloids (e.g., [6RS]-[2E,7E,9E]-6-hydroxy-N-[2-hydroxy-2-methylpropyl]-11-oxo-2,7,9-dodecatrienamide and [2E,7E,9E]-N-[2-hydroxy-2-methylpropyl]-11-ethoxy-6-hydroxy-dodeca-2,7,9-trienamide). Also, the 66 main targets were filtered from 746 predicted targets and 928 pain-related targets through module Network Analyzer in Cytoscape 3.6.0. Finally, there were 3 critical signaling pathways, including mitogen-activated protein kinase, phosphoinositide 3-kinase-protein kinase B-mammalian target of rapamycin, and IκB kinase-nuclear factor κB-cyclooxygenase 2 based on integrated discovery with 54 enriched signaling pathways.

Conclusions: HJ is used as a pain relief and has multicomponents, multitargets, and multiapproaches. Amide alkaloids are important substance bases, and HJ is more suitable for treating inflammatory pain.