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Axonal degeneration and demyelination following traumatic spinal cord injury: A systematic review and meta-analysis.创伤性脊髓损伤后轴突变性和脱髓鞘:系统评价和荟萃分析。
J Chem Neuroanat. 2019 Apr;97:9-22. doi: 10.1016/j.jchemneu.2019.01.009. Epub 2019 Feb 3.
2
Epidural Spinal Cord Stimulation Facilitates Immediate Restoration of Dormant Motor and Autonomic Supraspinal Pathways after Chronic Neurologically Complete Spinal Cord Injury.硬膜外脊髓电刺激促进慢性完全性脊髓损伤后休眠的运动和自主神经上位通路的即刻恢复。
J Neurotrauma. 2019 Aug 1;36(15):2325-2336. doi: 10.1089/neu.2018.6006. Epub 2019 Mar 6.
3
Spinal Cord Stimulation for Pain Treatment After Spinal Cord Injury.脊髓刺激治疗脊髓损伤后疼痛。
Neurosci Bull. 2019 Jun;35(3):527-539. doi: 10.1007/s12264-018-0320-9. Epub 2018 Dec 17.
4
Olig2-expressing Mesenchymal Stem Cells Enhance Functional Recovery after Contusive Spinal Cord Injury.表达少突胶质细胞转录因子2的间充质干细胞可促进脊髓挫伤损伤后的功能恢复。
Int J Stem Cells. 2018 Nov 30;11(2):177-186. doi: 10.15283/ijsc18071.
5
Targeted neurotechnology restores walking in humans with spinal cord injury.靶向神经技术恢复脊髓损伤患者的行走能力。
Nature. 2018 Nov;563(7729):65-71. doi: 10.1038/s41586-018-0649-2. Epub 2018 Oct 31.
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Neuromodulation in the restoration of function after spinal cord injury.脊髓损伤后功能恢复中的神经调节。
Lancet Neurol. 2018 Oct;17(10):905-917. doi: 10.1016/S1474-4422(18)30287-4. Epub 2018 Sep 18.
7
Silencing of PHLPP1 promotes neuronal apoptosis and inhibits functional recovery after spinal cord injury in mice.PHLPP1 的沉默促进小鼠脊髓损伤后的神经元凋亡,并抑制功能恢复。
Life Sci. 2018 Sep 15;209:291-299. doi: 10.1016/j.lfs.2018.08.030. Epub 2018 Aug 13.
8
Amiloride Promotes Oligodendrocyte Survival and Remyelination after Spinal Cord Injury in Rats.阿米洛利可促进大鼠脊髓损伤后少突胶质细胞存活及髓鞘再生。
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Neurosci Bull. 2018 Apr;34(2):247-260. doi: 10.1007/s12264-018-0207-9. Epub 2018 Feb 3.
10
The Protective Effect of Spinal Cord Stimulation Postconditioning Against Spinal Cord Ischemia/Reperfusion Injury in Rabbits.脊髓刺激后处理对兔脊髓缺血/再灌注损伤的保护作用
Neuromodulation. 2018 Jul;21(5):448-456. doi: 10.1111/ner.12751. Epub 2018 Jan 18.

硬膜外脊髓电刺激通过增强少突胶质细胞的存活和分化并保护脊髓损伤后的髓鞘来促进运动功能恢复。

Epidural Spinal Cord Stimulation Promotes Motor Functional Recovery by Enhancing Oligodendrocyte Survival and Differentiation and by Protecting Myelin after Spinal Cord Injury in Rats.

机构信息

Department of Orthopedics, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, 200072, China.

Spinal Pain Research Institute, Tongji University School of Medicine, Shanghai, 200072, China.

出版信息

Neurosci Bull. 2020 Apr;36(4):372-384. doi: 10.1007/s12264-019-00442-0. Epub 2019 Nov 16.

DOI:10.1007/s12264-019-00442-0
PMID:31732865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7142180/
Abstract

Epidural spinal cord stimulation (ESCS) markedly improves motor and sensory function after spinal cord injury (SCI), but the underlying mechanisms are unclear. Here, we investigated whether ESCS affects oligodendrocyte differentiation and its cellular and molecular mechanisms in rats with SCI. ESCS improved hindlimb motor function at 7 days, 14 days, 21 days, and 28 days after SCI. ESCS also significantly increased the myelinated area at 28 days, and reduced the number of apoptotic cells in the spinal white matter at 7 days. SCI decreased the expression of 2',3'-cyclic-nucleotide 3'-phosphodiesterase (CNPase, an oligodendrocyte marker) at 7 days and that of myelin basic protein at 28 days. ESCS significantly upregulated these markers and increased the percentage of Sox2/CNPase/DAPI-positive cells (newly differentiated oligodendrocytes) at 7 days. Recombinant human bone morphogenetic protein 4 (rhBMP4) markedly downregulated these factors after ESCS. Furthermore, ESCS significantly decreased BMP4 and p-Smad1/5/9 expression after SCI, and rhBMP4 reduced this effect of ESCS. These findings indicate that ESCS enhances the survival and differentiation of oligodendrocytes, protects myelin, and promotes motor functional recovery by inhibiting the BMP4-Smad1/5/9 signaling pathway after SCI.

摘要

硬膜外脊髓电刺激(ESCS)显著改善脊髓损伤(SCI)后的运动和感觉功能,但潜在机制尚不清楚。在这里,我们研究了 ESCS 是否会影响 SCI 大鼠的少突胶质细胞分化及其细胞和分子机制。ESCS 可改善 SCI 后 7 天、14 天、21 天和 28 天的后肢运动功能。ESCS 还可显著增加 28 天时的髓鞘面积,并减少 7 天时脊髓白质中的凋亡细胞数量。SCI 可降低 7 天时 2',3'-环核苷酸 3'-磷酸二酯酶(CNPase,少突胶质细胞标志物)的表达和 28 天时髓鞘碱性蛋白的表达。ESCS 可显著上调这些标志物,并增加 Sox2/CNPase/DAPI 阳性细胞(新分化的少突胶质细胞)的百分比在 7 天时。重组人骨形态发生蛋白 4(rhBMP4)在 ESCS 后明显下调了这些因子。此外,ESCS 可显著降低 SCI 后 BMP4 和 p-Smad1/5/9 的表达,而 rhBMP4 则降低了 ESCS 的这种作用。这些发现表明,ESCS 通过抑制 BMP4-Smad1/5/9 信号通路,增强少突胶质细胞的存活和分化,保护髓鞘,并促进运动功能恢复。