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本文引用的文献

1
Systemic polyethylene glycol promotes neurological recovery and tissue sparing in rats after cervical spinal cord injury.全身应用聚乙二醇可促进大鼠颈脊髓损伤后的神经功能恢复并减少组织损伤。
J Neuropathol Exp Neurol. 2009 Jun;68(6):661-76. doi: 10.1097/NEN.0b013e3181a72605.
2
Atorvastatin prevents early apoptosis after thoracic spinal cord contusion injury and promotes locomotion recovery.阿托伐他汀可预防胸段脊髓挫伤损伤后的早期细胞凋亡,并促进运动功能恢复。
Neurosci Lett. 2009 Mar 27;453(1):73-6. doi: 10.1016/j.neulet.2009.01.062. Epub 2009 Jan 29.
3
Recombinant human erythropoietin protects against experimental spinal cord trauma injury by regulating expression of the proteins MKP-1 and p-ERK.重组人促红细胞生成素通过调节MKP-1和p-ERK蛋白的表达来预防实验性脊髓创伤损伤。
J Int Med Res. 2009 Mar-Apr;37(2):511-9. doi: 10.1177/147323000903700227.
4
Effectiveness of riluzole in suppressing spasticity in the spinal cord injured rat.利鲁唑对脊髓损伤大鼠痉挛的抑制作用
Neurosci Lett. 2009 May 15;455(2):150-3. doi: 10.1016/j.neulet.2009.03.016. Epub 2009 Mar 11.
5
Systemic hypothermia improves histological and functional outcome after cervical spinal cord contusion in rats.全身低温可改善大鼠颈髓挫伤后的组织学和功能结局。
J Comp Neurol. 2009 Jun 10;514(5):433-48. doi: 10.1002/cne.22014.
6
Magnesium chloride in a polyethylene glycol formulation as a neuroprotective therapy for acute spinal cord injury: preclinical refinement and optimization.聚乙二醇制剂中氯化镁作为急性脊髓损伤的神经保护治疗:临床前细化和优化。
J Neurotrauma. 2009 Aug;26(8):1379-93. doi: 10.1089/neu.2009.0884.
7
Gene expression profiling in anti-CD11d mAb-treated spinal cord-injured rats.抗CD11d单克隆抗体治疗的脊髓损伤大鼠的基因表达谱分析。
J Neuroimmunol. 2009 Apr 30;209(1-2):104-13. doi: 10.1016/j.jneuroim.2009.02.002. Epub 2009 Feb 27.
8
Ibuprofen enhances recovery from spinal cord injury by limiting tissue loss and stimulating axonal growth.布洛芬通过限制组织损失和刺激轴突生长来促进脊髓损伤的恢复。
J Neurotrauma. 2009 Jan;26(1):81-95. doi: 10.1089/neu.2007.0464.
9
Peroxisome proliferator-activated receptor gamma pathway targeting in carcinogenesis: implications for chemoprevention.过氧化物酶体增殖物激活受体γ通路在致癌作用中的靶向作用:对化学预防的意义。
Clin Cancer Res. 2009 Jan 1;15(1):2-8. doi: 10.1158/1078-0432.CCR-08-0326.
10
Effects of progesterone on oligodendrocyte progenitors, oligodendrocyte transcription factors, and myelin proteins following spinal cord injury.脊髓损伤后孕酮对少突胶质前体细胞、少突胶质细胞转录因子及髓鞘蛋白的影响。
Glia. 2009 Jun;57(8):884-97. doi: 10.1002/glia.20814.

急性脊髓损伤的非侵入性药物神经保护治疗的系统评价。

A systematic review of non-invasive pharmacologic neuroprotective treatments for acute spinal cord injury.

机构信息

University of British Columbia, Combined Neurosurgical and Orthopaedic Spine Program, Department of Orthopaedics, Vancouver, British Columbia, Canada.

出版信息

J Neurotrauma. 2011 Aug;28(8):1545-88. doi: 10.1089/neu.2009.1149. Epub 2010 Apr 14.

DOI:10.1089/neu.2009.1149
PMID:20146558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3143410/
Abstract

An increasing number of therapies for spinal cord injury (SCI) are emerging from the laboratory and seeking translation into human clinical trials. Many of these are administered as soon as possible after injury with the hope of attenuating secondary damage and maximizing the extent of spared neurologic tissue. In this article, we systematically review the available pre-clinical research on such neuroprotective therapies that are administered in a non-invasive manner for acute SCI. Specifically, we review treatments that have a relatively high potential for translation due to the fact that they are already used in human clinical applications, or are available in a form that could be administered to humans. These include: erythropoietin, NSAIDs, anti-CD11d antibodies, minocycline, progesterone, estrogen, magnesium, riluzole, polyethylene glycol, atorvastatin, inosine, and pioglitazone. The literature was systematically reviewed to examine studies in which an in-vivo animal model was utilized to assess the efficacy of the therapy in a traumatic SCI paradigm. Using these criteria, 122 studies were identified and reviewed in detail. Wide variations exist in the animal species, injury models, and experimental designs reported in the pre-clinical literature on the therapies reviewed. The review highlights the extent of investigation that has occurred in these specific therapies, and points out gaps in our knowledge that would be potentially valuable prior to human translation.

摘要

越来越多的脊髓损伤 (SCI) 治疗方法正在从实验室中涌现,并寻求转化为人体临床试验。许多治疗方法在受伤后尽快进行,希望减轻继发性损伤并最大限度地保留神经组织。在本文中,我们系统地回顾了这些非侵入性急性 SCI 神经保护治疗方法的可用临床前研究。具体来说,我们回顾了那些由于已经在人类临床应用中使用,或者可以以可用于人类的形式提供而具有较高转化潜力的治疗方法。这些方法包括:促红细胞生成素、非甾体抗炎药、抗 CD11d 抗体、米诺环素、孕酮、雌激素、镁、利鲁唑、聚乙二醇、阿托伐他汀、肌苷和吡格列酮。系统地审查了文献,以检查在创伤性 SCI 范式中利用体内动物模型评估治疗效果的研究。使用这些标准,确定了 122 项研究,并进行了详细审查。在综述的治疗方法的临床前文献中,动物物种、损伤模型和实验设计存在广泛差异。该综述强调了这些特定疗法的研究程度,并指出了在人类转化之前可能有价值的知识空白。