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RSC Adv. 2020 Jul 21;10(45):27194-27214. doi: 10.1039/d0ra04736h. eCollection 2020 Jul 15.
2
Protein post-translational modifications after spinal cord injury.脊髓损伤后的蛋白质翻译后修饰
Neural Regen Res. 2021 Oct;16(10):1935-1943. doi: 10.4103/1673-5374.308068.
3
Selenium-Doped Carbon Quantum Dots Efficiently Ameliorate Secondary Spinal Cord Injury via Scavenging Reactive Oxygen Species.硒掺杂碳量子点通过清除活性氧来有效改善继发性脊髓损伤。
Int J Nanomedicine. 2020 Dec 14;15:10113-10125. doi: 10.2147/IJN.S282985. eCollection 2020.
4
Cerium oxide nanoparticles as a new neuroprotective agent to promote functional recovery in a rat model of sciatic nerve crush injury.氧化铈纳米颗粒作为一种新型神经保护剂促进大鼠坐骨神经挤压伤模型功能恢复。
Br J Neurosurg. 2024 Apr;38(2):301-306. doi: 10.1080/02688697.2020.1864292. Epub 2020 Dec 26.
5
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Physiol Behav. 2021 Jan 1;228:113186. doi: 10.1016/j.physbeh.2020.113186. Epub 2020 Sep 25.
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Novel Approach for Efficient Recovery for Spinal Cord Injury Repair via Biofabricated Nano-Cerium Oxide Loaded PCL With Resveratrol to Improve in Vitro Biocompatibility and Autorecovery Abilities.通过生物制造的负载白藜芦醇的纳米氧化铈聚己内酯实现脊髓损伤修复高效恢复的新方法,以提高体外生物相容性和自我恢复能力。
Dose Response. 2020 Sep 2;18(3):1559325820933518. doi: 10.1177/1559325820933518. eCollection 2020 Jul-Sep.
7
Tau Pathology Triggered by Spinal Cord Injury Can Play a Critical Role in the Neurotrauma Development.脊髓损伤引发的 Tau 病理学在神经创伤发展中可发挥关键作用。
Mol Neurobiol. 2020 Nov;57(11):4845-4855. doi: 10.1007/s12035-020-02061-7. Epub 2020 Aug 18.
8
Myelin Associated Inhibitory Proteins as a Therapeutic Target for Healing of CNS Injury.髓鞘相关抑制蛋白作为中枢神经系统损伤修复的治疗靶点。
ACS Chem Neurosci. 2020 Jun 17;11(12):1699-1700. doi: 10.1021/acschemneuro.0c00280. Epub 2020 Jun 2.
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Effect of Cerium Oxide Nanoparticles on Oxidative Stress Biomarkers in Rats' Kidney, Lung, and Serum.氧化铈纳米颗粒对大鼠肾脏、肺和血清氧化应激生物标志物的影响。
Iran Biomed J. 2020 Jul;24(4):251-6. doi: 10.29252/ibj.24.4.251. Epub 2020 Feb 10.

注射氧化铈纳米颗粒治疗大鼠脊髓损伤

Injection of Cerium Oxide Nanoparticles to Treat Spinal Cord Injury in Rats.

作者信息

Behroozi Zahra, Rahimi Behnaz, Hamblin Michael R, Nasirinezhad Farinaz, Janzadeh Atousa, Ramezani Fatemeh

机构信息

From the Physiology Research Center, Institute of Neuropharmaclogy, Kerman University of Medical Sciences. Kerman, Iran.

Department of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

出版信息

J Neuropathol Exp Neurol. 2022 Jul 19;81(8):635-642. doi: 10.1093/jnen/nlac026.

DOI:10.1093/jnen/nlac026
PMID:35472142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9297098/
Abstract

This study investigated the effects of local injection of cerium oxide nanoparticles (CeONPs) in a rat spinal cord injury (SCI) model. Thirty-six adult male Wistar rats were divided into 4 groups: controls (healthy animals), sham (laminectomy), SCI (laminectomy+SCI induction), and treatment (laminectomy+SCI induction+intrathecal injection of CeONPs immediately after injury). SCI was induced using an aneurysm clip at the T12-T13 vertebral region. Motor performance and pain threshold tests were performed weekly; H&E staining and measurement of cavity sizes were performed 6 weeks after injury. The expression of granulocyte colony-stimulating factor (GCSF), P44/42 MAPK, P-P44/42 MAPK, Tau, myelin-associated glycoprotein(MAG) was evaluated after 6 weeks by Western blot. The Basso, Beattie, and Bresnahan locomotor scoring scales improved in animals receiving CeONPs compared with SCI animals. The cavity sizes were less in the treatment group. GCSF expression was similar in the animals receiving CeONPs compared with the SCI group but the expression of ERK1/ERK2 and phospho-ERK was lower than in the SCI group. Expression levels of Tau and MAG were significantly increased in treated animals compared to the SCI group. These data indicate that the use of CeONPs may improve motor functional recovery in SCI.

摘要

本研究调查了在大鼠脊髓损伤(SCI)模型中局部注射氧化铈纳米颗粒(CeONPs)的效果。36只成年雄性Wistar大鼠被分为4组:对照组(健康动物)、假手术组(椎板切除术)、SCI组(椎板切除术+SCI诱导)和治疗组(椎板切除术+SCI诱导+损伤后立即鞘内注射CeONPs)。在T12 - T13椎体区域使用动脉瘤夹诱导SCI。每周进行运动性能和疼痛阈值测试;损伤6周后进行苏木精-伊红(H&E)染色和空洞大小测量。6周后通过蛋白质印迹法评估粒细胞集落刺激因子(GCSF)、P44/42丝裂原活化蛋白激酶(MAPK)、磷酸化P44/42 MAPK、微管相关蛋白Tau、髓鞘相关糖蛋白(MAG)的表达。与SCI动物相比,接受CeONPs的动物的Basso、Beattie和Bresnahan运动评分量表有所改善。治疗组的空洞尺寸较小。与SCI组相比,接受CeONPs的动物中GCSF表达相似,但ERK1/ERK2和磷酸化ERK的表达低于SCI组。与SCI组相比,治疗动物中Tau和MAG的表达水平显著增加。这些数据表明,使用CeONPs可能会改善SCI中的运动功能恢复。