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Synergetic Use of Neural Precursor Cells and Self-assembling Peptides in Experimental Cervical Spinal Cord Injury
Published on: February 23, 2015
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Promoting spinal cord injury repair by using ZnO@MOFs nanozymes functionalized hydrogel through the ROS
Jiaxin Ding1,2,3, Binbin Gao4, Zelin Sang3,5
1Dalian Medical University, Dalian, 116044, China.
Regenerative Biomaterials
|November 5, 2025
Summary
A novel nanotherapeutic, ZnO-ZIF8@H, combined with near-infrared (NIR) irradiation, effectively reduces oxidative stress and neuronal apoptosis in spinal cord injury (SCI) models. This photothermal nanotechnology offers a promising therapeutic strategy for mitigating secondary damage.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Neuroscience
Background:
- Spinal cord injury (SCI) causes significant patient recovery challenges due to oxidative stress and neuronal apoptosis.
- Photothermal nanotechnology presents a novel therapeutic avenue for SCI treatment.
- Developing targeted nanotherapeutics is crucial for enhancing treatment outcomes.
Purpose of the Study:
- To develop and evaluate a novel nanotherapeutic system, ZnO-ZIF8@H, for treating spinal cord injury.
- To investigate the efficacy of ZnO-ZIF8@H combined with near-infrared (NIR) irradiation in mitigating SCI-induced damage.
- To assess the impact of the treatment on oxidative stress markers and neuronal apoptosis.
Main Methods:
- Development of a ZnO-ZIF8@H nanotherapeutic system.
- Application of the nanotherapeutic system combined with NIR irradiation on SCI models.
- Measurement of malondialdehyde (MDA) levels to assess lipid peroxidation.
- Assay of superoxide dismutase (SOD) and glutathione (GSH) enzyme activity.
- TUNEL staining and Cleaved-Caspase3 expression analysis in NeuN-positive neurons to evaluate apoptosis.
Main Results:
- ZnO-ZIF8@H + NIR irradiation significantly reduced oxidative stress markers, including decreased MDA levels.
- The treatment enhanced the activity of antioxidant enzymes, SOD and GSH.
- Neuronal apoptosis was suppressed, as indicated by reduced TUNEL staining and Cleaved-Caspase3 expression in neurons.
- The combined therapy effectively alleviated secondary damage following spinal cord injury.
Conclusions:
- The ZnO-ZIF8@H nanotherapeutic system combined with NIR irradiation demonstrates significant neuroprotective effects against SCI.
- This approach effectively mitigates secondary injury by reducing oxidative stress and inhibiting neuronal apoptosis.
- ZnO-ZIF8@H + NIR represents a promising therapeutic strategy for spinal cord injury management.

