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脊髓损伤中的炎症与细胞凋亡。

Inflammation & apoptosis in spinal cord injury.

机构信息

Department of Orthopaedics, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Indian J Med Res. 2012 Mar;135(3):287-96.

PMID:22561613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3361863/
Abstract

Spinal cord injury (SCI) consists of a two-steps process involving a primary mechanical injury followed by an inflammatory process and apoptosis. Secondary insult is characterized by further destruction of neuronal and glial cells, and leads to expansion of the damage, so that the paralysis can extend to higher segments. With the identification of mechanisms that either promote or prevent neuronal inflammation and apoptosis come new approaches for preventing and treating neurodegenerative disorders. From a clinical perspective, this article discusses novel targets for the development of therapeutic agents that have the potential to protect the spinal cord from irreversible damage and promote functional recovery.

摘要

脊髓损伤(SCI)由两个步骤组成,包括原发性机械损伤,随后是炎症过程和细胞凋亡。继发性损伤的特征是神经元和神经胶质细胞的进一步破坏,并导致损伤扩大,从而使瘫痪扩展到更高的节段。随着促进或预防神经元炎症和细胞凋亡的机制的确定,出现了预防和治疗神经退行性疾病的新方法。从临床角度来看,本文讨论了开发治疗药物的新靶点,这些药物有可能保护脊髓免受不可逆转的损伤并促进功能恢复。

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本文引用的文献

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Spinal Cord. 2011 Mar;49(3):337-44. doi: 10.1038/sc.2010.127. Epub 2010 Sep 28.
2
Body cooling ameliorating spinal cord injury may be neurogenesis-, anti-inflammation- and angiogenesis-associated in rats.体温降低改善大鼠脊髓损伤可能与神经发生、抗炎及血管生成相关。
J Trauma. 2011 Apr;70(4):885-93. doi: 10.1097/TA.0b013e3181e7456d.
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Microarray analysis of expression of cell death-associated genes in rat spinal cord cells exposed to cyclic tensile stresses in vitro.体外循环拉伸应力作用下大鼠脊髓细胞细胞凋亡相关基因表达的基因芯片分析。
BMC Neurosci. 2010 Jul 22;11:84. doi: 10.1186/1471-2202-11-84.
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A model for ex vivo spinal cord segment culture--a tool for analysis of injury repair strategies.离体脊髓节段培养模型——一种分析损伤修复策略的工具。
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Evaluation of protective effects of the alpha lipoic acid after spinal cord injury: an animal study.评估α-硫辛酸对脊髓损伤后的保护作用:一项动物研究。
Injury. 2010 Oct;41(10):1068-74. doi: 10.1016/j.injury.2010.05.027.
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Inflammatory hyperalgesia induces essential bioactive lipid production in the spinal cord.炎症性痛觉过敏会在脊髓中引起必需的生物活性脂质的产生。
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Selective adenosine A(2a) receptor agonists reduce the apoptosis in an experimental model of spinal cord trauma.选择性腺苷 A(2a)受体激动剂可减少脊髓创伤实验模型中的细胞凋亡。
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Immunization with neural-derived antigens inhibits lipid peroxidation after spinal cord injury.免疫神经来源抗原可抑制脊髓损伤后的脂质过氧化。
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