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本文引用的文献

1
Umbilical cord blood banking: an update.脐带血库:更新。
J Assist Reprod Genet. 2011 Aug;28(8):669-76. doi: 10.1007/s10815-011-9577-x. Epub 2011 May 27.
2
Control of the embryonic stem cell state.胚胎干细胞状态的控制。
Cell. 2011 Mar 18;144(6):940-54. doi: 10.1016/j.cell.2011.01.032.
3
Stem cells for spinal cord regeneration: Current status.用于脊髓再生的干细胞:现状
Surg Neurol Int. 2010 Dec 25;1:93. doi: 10.4103/2152-7806.74240.
4
Histological repair of damaged spinal cord tissue from chronic contusion injury of rat: a LM observation.大鼠慢性挫伤性脊髓损伤组织的组织学修复:LM 观察。
Histol Histopathol. 2011 Jan;26(1):45-58. doi: 10.14670/HH-26.45.
5
Glial scar and neuroregeneration: histological, functional, and magnetic resonance imaging analysis in chronic spinal cord injury.胶质瘢痕与神经再生:慢性脊髓损伤的组织学、功能学及磁共振成像分析。
J Neurosurg Spine. 2010 Aug;13(2):169-80. doi: 10.3171/2010.3.SPINE09190.
6
Scarring after spinal cord injury.脊髓损伤后的瘢痕形成。
J Neurosurg Spine. 2010 Aug;13(2):165-7; discussion 167-8. doi: 10.3171/2009.11.SPINE09862.
7
Triptolide promotes spinal cord repair by inhibiting astrogliosis and inflammation.雷公藤内酯醇通过抑制星形胶质细胞增生和炎症反应促进脊髓修复。
Glia. 2010 Jun;58(8):901-15. doi: 10.1002/glia.20972.
8
Transplanted olfactory mucosal cells restore paw reaching function without regeneration of severed corticospinal tract fibres across the lesion.移植嗅黏膜细胞可恢复前肢抓握功能,而无需再生损伤处的切断皮质脊髓束纤维。
Brain Res. 2009 Dec 15;1303:26-31. doi: 10.1016/j.brainres.2009.09.073. Epub 2009 Sep 24.
9
NG2 and phosphacan are present in the astroglial scar after human traumatic spinal cord injury.在人类创伤性脊髓损伤后的星形胶质瘢痕中存在神经聚糖(NG2)和磷酸软骨素蛋白聚糖。
BMC Neurol. 2009 Jul 15;9:32. doi: 10.1186/1471-2377-9-32.
10
Spinal cord injury reveals multilineage differentiation of ependymal cells.脊髓损伤揭示了室管膜细胞的多谱系分化。
PLoS Biol. 2008 Jul 22;6(7):e182. doi: 10.1371/journal.pbio.0060182.

脊髓损伤:从炎症到胶质瘢痕

Spinal cord injury: From inflammation to glial scar.

作者信息

Leal-Filho Manoel Baldoino

机构信息

Department of Neurosurgery, Casamater Hospital, Teresina, PI, Brazil.

出版信息

Surg Neurol Int. 2011;2:112. doi: 10.4103/2152-7806.83732. Epub 2011 Aug 13.

DOI:10.4103/2152-7806.83732
PMID:21886885
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3162797/
Abstract

BACKGROUND

Glial scar (GS) is the most important inhibitor factor to neuroregeneration after spinal cord injury (SCI) and behaves as a tertiary lesion. The present review of the literature searched for representative studies concerning GS and therapeutic strategies to neuroregeneration.

METHODS

The author used the PubMed database and Google scholar to search articles published in the last 20 years. Key words used were SCI, spinal cord (SC) inflammation, GS, and SCI treatment.

RESULTS

Both inflammation and GS are considered important events after SCI. Despite the fact that firstly they seem to cause benefit, in the end they cause more harm than good to neuroregeneration. Each stage has its own aspects under the influence of the immune system causing inflammation, from the primary to secondary lesion and from those to GS (tertiary lesion).

CONCLUSION

Future studies should stress the key points where and when GS presents itself as an inhibitory factor to neuroregeneration. Considering GS as an important event after SCI, the author defends GS as being a tertiary lesion. Current strategies are presented with emphasis on stem cells and drug therapy. A better understanding will permit the development of a therapeutic basis in the treatment of the SCI patients considering each stage of the lesion, with emphasis on GS and neuroregeneration.

摘要

背景

胶质瘢痕(GS)是脊髓损伤(SCI)后神经再生最重要的抑制因素,表现为三级损伤。本综述检索了有关GS及神经再生治疗策略的代表性研究。

方法

作者使用PubMed数据库和谷歌学术搜索过去20年发表的文章。使用的关键词为SCI、脊髓(SC)炎症、GS和SCI治疗。

结果

炎症和GS均被认为是SCI后的重要事件。尽管它们最初似乎有益,但最终对神经再生弊大于利。在免疫系统引起炎症的影响下,从原发性损伤到继发性损伤,再到GS(三级损伤),每个阶段都有其自身特点。

结论

未来的研究应强调GS在何时何地成为神经再生抑制因素的关键点。考虑到GS是SCI后的一个重要事件,作者认为GS是一种三级损伤。目前的策略重点介绍了干细胞和药物治疗。更好地理解将有助于在考虑损伤各阶段的情况下,为SCI患者的治疗建立治疗基础,重点是GS和神经再生。