Related Experiment Video
Updated: Dec 6, 2025

07:50
Facilitating Drug Discovery: An Automated High-content Inflammation Assay in Zebrafish
Published on: July 16, 2012
14.6K
Zanthoxylum nitidum extract attenuates BMP-2-induced inflammation and hyperpermeability.
Tao Hu1, Zhiwen Luo2, Kai Li3
1Department of Spine Surgery, Shanghai East Hospital, Tongji University School of Medicine, China.
Bioscience Reports
|October 8, 2020
Summary
Zanthoxylum nitidum (ZN) mitigates inflammation and vascular hyper-permeability caused by bone morphogenetic protein-2 (BMP-2) in spinal surgery. This natural compound offers a potential therapeutic strategy against BMP-2-related side effects.
Area of Science:
- Biomedical Engineering
- Pharmacology
- Cell Biology
Background:
- Bone morphogenetic protein-2 (BMP-2) is widely used in spinal fusion surgery.
- BMP-2 can cause adverse effects, including vascular hyper-permeability and inflammation.
- There is a need for effective countermeasures against BMP-2-induced side effects.
Purpose of the Study:
- To investigate the protective effects of Zanthoxylum nitidum (ZN) against BMP-2-induced inflammation and hyper-permeability.
- To elucidate the underlying molecular mechanisms of ZN's protective action.
- To assess ZN as a potential therapeutic agent for BMP-2-related complications.
Main Methods:
- Human umbilical vein endothelial cells (HUVECs) were treated with BMP-2 and ZN.
- Pro-inflammatory cytokine levels (IL-1α, IL-1β, TNF-α) were measured.
- NF-κB signaling pathway activation (p65, IκB phosphorylation, nuclear translocation) was assessed.
- Expression of tight junction proteins (VE-cadherin, Occludin) was analyzed.
- Vascular hyper-permeability was evaluated using dextran-fluorescein intensity.
Main Results:
- BMP-2 significantly increased pro-inflammatory cytokine production in HUVECs.
- ZN suppressed BMP-2-induced increases in IL-1α, IL-1β, and TNF-α.
- ZN inhibited BMP-2-induced NF-κB pathway activation and p65 nuclear translocation.
- ZN restored BMP-2-impaired expression of VE-cadherin and Occludin.
- ZN reversed BMP-2-induced HUVEC hyper-permeability.
Conclusions:
- Zanthoxylum nitidum (ZN) effectively antagonizes BMP-2-induced inflammation and vascular hyper-permeability.
- ZN acts by inhibiting the NF-κB signaling pathway and preserving endothelial barrier integrity.
- ZN demonstrates potential as a therapeutic candidate to manage BMP-2-related adverse effects in spinal fusion.

