The Inhibition of Inflammatory Signaling Pathway by Secretory Leukocyte Protease Inhibitor can Improve Spinal Cord Injury.

Abstract

Spinal cord injury leads to loss of sensory motor functions below the damaged area, and can significantly affects physical and mental health. An effective spinal cord injury treatment is currently unavailable, in part, because of the intricacy of the brain, as well as the complex pathophysiological mechanism of the injury. Inflammation is an important biological process in multitudinous diseases, with no exception for spinal cord injury. Nuclear factor kappa beta (NF-κB) signaling pathway is a key inflammatory element, as it is involved in cell survival, apoptosis, proliferation, differentiation, and immune response. Activation of the NF-κB signaling pathway leads to the release of a large number of inflammatory factors that can affect tissue repair. Hence, the inhibition of inflammatory responses could improve the repair of injured spinal cord tissues. Secretory leukocyte protease inhibitor (SLPI) has anti-inflammatory and anti-bacterial properties, and promotes wound healing. SLPI can bind to the promoter region of tumor necrosis factor-αand interleukin-8 (IL-8) to inhibit the NF-κB signaling pathway. Additionally, SLPI can reduce secondary damages after spinal cord injury, and prevent further complications. In this report, we analyze the pathophysiological mechanism of spinal cord injury, the role of NF-κB signaling pathway following spinal cord injury, and how SLPI regulates the NF-κB signaling pathway to curtail inflammatory reaction.

• Authors: Renzhe Tang, Benson O A Botchway, Yanfeng Meng, Yong Zhang, Conghui Zhou, Junsong Jiang, Xuehong Liu
• Journal: Cellular and molecular neurobiology (Cell Mol Neurobiol) Vol. 40 Issue 7 Pg. 1067-1073 (Oct 2020) ISSN: 1573-6830 [Electronic] United States
• PMID: 31993863 (Publication Type: Journal Article, Review)

Chemical References

• Anti-Inflammatory Agents
• Tumor Necrosis Factor-alpha

Topics

• Animals
• Anti-Inflammatory Agents (pharmacology)
• Humans
• Inflammation (drug therapy, metabolism)
• Signal Transduction (drug effects, physiology)
• Spinal Cord (drug effects, metabolism)
• Spinal Cord Injuries (drug therapy, metabolism)
• Tumor Necrosis Factor-alpha (pharmacology)