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Updated: Jul 12, 2026

Synergetic Use of Neural Precursor Cells and Self-assembling Peptides in Experimental Cervical Spinal Cord Injury
Published on: February 23, 2015
A novel schisantherin B-loaded Prussian blue nanozyme for treating spinal cord injury
Wei Wang1,2,3, Ensi Liu4, Jinxia Wang5
1Graduate School of Dalian Medical University, Dalian 116044, Liaoning, China.
Abstract:
Spinal cord injury (SCI) encompasses a series of pathophysiological processes, including inflammation, apoptosis, autophagy, and pyroptosis, leading to an imbalance in the microenvironment. The microenvironment following injury inhibits axonal regeneration, ultimately resulting in the loss of neurological function. Among these pathological processes, inflammation plays a critical role in the recovery from SCI. The inflammatory cascade triggered by SCI leads to cell apoptosis, cell death, and impaired angiogenesis, which collectively hinder axonal regeneration. In recent years, nano-enzymes exhibiting Prussian blue enzyme-like peroxidase activity have garnered significant attention as alternatives to natural enzymes in therapeutic applications, biosensing, and environmental remediation. Schisandra, a traditional Chinese medicine, contains schisantherin B as its principal component, which has been reported to possess neuroprotective effects in various neurological diseases. In this study, we designed a Prussian blue nanozyme drug delivery system, a schisantherin B-loaded Prussian blue nanozyme (SchB@PBzyme), for the treatment of SCI. Our findings indicate that the SchB@PBzyme significantly suppresses the inflammatory response and promotes neural remodeling, thereby offering a novel treatment strategy for SCI.
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