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聚乙二醇干扰素-β在颈脊髓挫伤后结合强制运动可调节急性炎症反应和恢复。

PEGylated interferon-beta modulates the acute inflammatory response and recovery when combined with forced exercise following cervical spinal contusion injury.

机构信息

Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA 19129, USA.

出版信息

Exp Neurol. 2010 Jun;223(2):439-51. doi: 10.1016/j.expneurol.2010.01.009. Epub 2010 Jan 28.

Abstract

Secondary degeneration leads to an expansion of the initial tissue damage sustained during a spinal cord injury (SCI). Dampening the cellular inflammatory response that contributes to this progressive tissue damage is one possible strategy for neuroprotection after acute SCI. We initially examined whether treatment with a PEGylated form of rat interferon-beta (IFN-beta) would modulate the expression of several markers of inflammation and neuroprotection at the site of a unilateral cervical level 5 contusion injury. Adult female Sprague-Dawley rats were injured using the Infinite Horizon Impactor at a force of 200 kdyn (equivalent to a severe injury) and a mean displacement of 1600-1800 mum. A single dose (5x10(6) units) of PEGylated IFN-beta or vehicle was administered 30 min following SCI. Here we demonstrate temporal changes in pro- and anti-inflammatory cytokine levels and the expression of heat shock proteins and iNOS (involved in neuroprotection) at the lesion epicenter and one segment caudally after SCI and PEG IFN-beta treatment. The results suggested a potential therapeutic treatment strategy for modulation of secondary damage after acute SCI. Therefore, we examined whether acute treatment with PEG IFN-beta would improve forelimb function alone or when combined with forced exercise (Ex). Animals began the Ex paradigm 5 days post SCI and continued for 5 days/week over 8 weeks. Locomotion (forelimb locomotor scale [FLS], hindlimb BBB, and TreadScan) and sensorimotor function (grid walking) was tested weekly. Additional outcome measures included lesion size and glial cell reactivity. Significant FLS improvements occurred at 1 week post SCI in the PEGylated IFN-beta-treated group but not at any other time point or with any other treatment approaches. These results suggest that this acute neuroprotective treatment strategy does not translate into long term behavioral recovery even when combined with forced exercise.

摘要

继发性退化导致脊髓损伤 (SCI) 期间初始组织损伤的扩大。抑制导致这种进行性组织损伤的细胞炎症反应是急性 SCI 后神经保护的一种可能策略。我们最初研究了聚乙二醇化形式的大鼠干扰素-β(IFN-β)治疗是否会调节单侧颈 5 挫伤损伤部位的几种炎症和神经保护标志物的表达。成年雌性 Sprague-Dawley 大鼠使用 Infinite Horizon 冲击器在 200 kdyn 的力(相当于严重损伤)和 1600-1800 mum 的平均位移下受伤。SCI 后 30 分钟给予单次剂量(5x10(6)单位)聚乙二醇化 IFN-β或载体。在这里,我们展示了 SCI 和 PEG IFN-β 治疗后损伤中心和一个节段尾部的促炎和抗炎细胞因子水平以及热休克蛋白和 iNOS(参与神经保护)表达的时间变化。结果表明,这是一种调节急性 SCI 后继发性损伤的潜在治疗策略。因此,我们研究了急性给予 PEG IFN-β 是否仅改善前肢功能,或与强制运动(Ex)联合使用时是否改善。动物在 SCI 后 5 天开始 Ex 范式,并在 8 周内每周进行 5 天/周。每周测试运动(前肢运动量表 [FLS]、后肢 BBB 和 TreadScan)和感觉运动功能(网格行走)。其他结果测量包括损伤大小和神经胶质细胞反应性。在 PEG IFN-β 治疗组中,在 SCI 后 1 周时 FLS 显著改善,但在其他任何时间点或使用任何其他治疗方法时均未改善。这些结果表明,即使与强制运动相结合,这种急性神经保护治疗策略也不会转化为长期行为恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133e/2864368/aa7a5668af15/nihms175237f1a.jpg

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