Promoting spinal cord injury repair by using ZnO@MOFs nanozymes functionalized hydrogel through the ROS microenvironment regulating pathway

氧化应激 脊髓损伤 神经保护 化学 脂质过氧化 丙二醛 细胞凋亡 超氧化物歧化酶 标记法 脊髓 活性氧 光热治疗 药理学 抗氧化剂 氧化损伤 谷胱甘肽 细胞生物学 癌症研究 氧化磷酸化 程序性细胞死亡 谷胱甘肽过氧化物酶 多发性硬化 神经科学
作者
Jiaxin Ding,Binbin Gao,Zelin Sang,Zhen Xiang Dai,Zhenhua Chen,Xifan Mei
出处
期刊:Regenerative Biomaterials [University of Oxford]
卷期号:12: rbaf095-rbaf095 被引量:8
标识
DOI:10.1093/rb/rbaf095
摘要

Spinal cord injury (SCI) is a kind of health problem characterized by oxidative stress and neuronal apoptosis, which pose major challenges to the recovery of patients. Recently, the application of photothermal nanotechnology in medicine has opened up exciting new avenues for the treatment of SCI. This innovative approach leverages the unique properties of nanomaterials to enhance therapeutic outcomes. In our study, we developed a novel nanotherapeutic system named ZnO-ZIF8@H, which is designed to deliver targeted neuroprotective effects. We meticulously evaluated its performance under near-infrared (NIR) irradiation, which is known to promote local heating and stimulate biological processes. The data indicated that the application of ZnO-ZIF8@H combined with NIR irradiation significantly reduced oxidative stress levels in the affected tissues. This was evidenced by a marked decrease in malondialdehyde (MDA) levels, a well-known indicator of lipid peroxidation and cellular damage. Simultaneously, the treatment notably enhanced the activity of superoxide dismutase (SOD) and glutathione (GSH) enzymes. These findings suggest that ZnO-ZIF8@H+NIR could both protect cells from oxidative damage and boost the internal antioxidant defenses, highlighting its potential as an effective therapeutic strategy for mitigating secondary injuries following spinal cord trauma. It also suppressed neuronal apoptosis, as evidenced by TUNEL staining and decreased Cleaved-Caspase3 expression in NeuN-positive neurons. These results indicated that ZnO-ZIF8@H+NIR effectively reduces secondary damage from SCI by alleviating apoptosis and oxidative stress, offering a promising approach for the therapy of SCI.
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