A Novel Network Pharmacology Strategy Based on the Universal Effectiveness-Common Mechanism of Medical Herbs Uncovers Therapeutic Targets in Traumatic Brain Injury

Drug Des Devel Ther. 2024 Apr 16:18:1175-1188. doi: 10.2147/DDDT.S450895. eCollection 2024.

Abstract

Purpose: Many herbs can promote neurological recovery following traumatic brain injury (TBI). There must lie a shared mechanism behind the common effectiveness. We aimed to explore the key therapeutic targets for TBI based on the common effectiveness of the medicinal plants.

Material and methods: The TBI-effective herbs were retrieved from the literature as imputes of network pharmacology. Then, the active ingredients in at least two herbs were screened out as common components. The hub targets of all active compounds were identified through Cytohubba. Next, AutoDock vina was used to rank the common compound-hub target interactions by molecular docking. A highly scored compound-target pair was selected for in vivo validation.

Results: We enrolled sixteen TBI-effective medicinal herbs and screened out twenty-one common compounds, such as luteolin. Ten hub targets were recognized according to the topology of the protein-protein interaction network of targets, including epidermal growth factor receptor (EGFR). Molecular docking analysis suggested that luteolin could bind strongly to the active pocket of EGFR. Administration of luteolin or the selective EGFR inhibitor AZD3759 to TBI mice promoted the recovery of body weight and neurological function, reduced astrocyte activation and EGFR expression, decreased chondroitin sulfate proteoglycans deposition, and upregulated GAP43 levels in the cortex. The effects were similar to those when treated with the selective EGFR inhibitor.

Conclusion: The common effectiveness-based, common target screening strategy suggests that inhibition of EGFR can be an effective therapy for TBI. This strategy can be applied to discover core targets and therapeutic compounds in other diseases.

Keywords: AZD3759; astrocyte; epidermal growth factor receptor; luteolin; medicinal plants; traditional Chinese medicine.

MeSH terms

  • Animals
  • Brain Injuries, Traumatic* / drug therapy
  • Brain Injuries, Traumatic* / metabolism
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / metabolism
  • Humans
  • Luteolin / chemistry
  • Luteolin / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Docking Simulation*
  • Network Pharmacology*
  • Plants, Medicinal / chemistry

Substances

  • ErbB Receptors
  • Luteolin

Grants and funding

This work was supported by the National Natural Science Foundation of China [grant number 82174259, 81973665], The Science and Technology Innovation Program of Hunan Province/the Hunan Provincial Key Research and Development Program [grant number 2023SK2021, 2022SK2015], the Hunan TCM Scientific Research Program [grant number 2021032, D2022065 and B2024113], The National Science Foundation of Hunan Province (2022JJ40853), and the Postdoctoral Fellowship Program of CPSF (GZC20233202).