首页> 外文期刊>Neurology India. >Combination of NEP 1-40 infusion and bone marrow-derived neurospheres transplantation inhibit glial scar formation and promote functional recovery after rat spinal cord injury.
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Combination of NEP 1-40 infusion and bone marrow-derived neurospheres transplantation inhibit glial scar formation and promote functional recovery after rat spinal cord injury.

机译:NEP 1-40输注与骨髓源性神经球移植相结合可抑制神经胶质瘢痕的形成并促进大鼠脊髓损伤后的功能恢复。

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BACKGROUND AND AIMS: Studies have shown that administration of NEP1-40, a Nogo-66 receptor antagonist peptide, improves locomotor recovery in rats. We hypothesize that combining NEP1-40 with another promising therapy, neural stem cell transplantation, might further improve the degree of locomotor recovery. In the present study, we examined whether NEP1-40 combined with bone marrow stromal cells-derived neurospheres (BMSC-NSs) transplantation would produce synergistic effects on recovery. MATERIAL AND METHODS: Adult Sprague-Dawley rats were subjected to spinal cord injury (SCI) at the T10 vertebral level. Immediately after injury, rats were administrated NEP1-40 intrathecally for 4 weeks. BrdU-labeled BMSC-NSs (2x105 ) were transplanted into the injured site 7 days after SCI. Locomotor recovery was assessed for 10 weeks with BBB scoring. Animals were perfused transcardially 10 weeks after contusion, and histological examinations were performed. RESULTS: The combined therapy group showed statistically better locomotor recovery than the control group at 7 weeks of contusion. Neither of the two single-agent treatments improved locomotor function. The average area of the cystic cavity was significantly smaller in the combined therapy group than in the control group. Fluorescence microscopic analysis showed that NEP1-40 dramatically inhibited the formation of glial scar and promoted the axons penetration into the scar barrier. CONCLUSION: This study revealed that BMSC-NSs and NEP 1-40 exhibit synergistic effects on recovery in rat SCI. This may represent a potential new strategy for the treatment of SCI.
机译:背景与目的:研究表明,施用NEP1-40(一种Nogo-66受体拮抗剂肽)可改善大鼠的运动恢复。我们假设将NEP1-40与另一种有前途的疗法神经干细胞移植结合起来,可能会进一步改善运动恢复的程度。在本研究中,我们检查了NEP1-40联合骨髓基质细胞源性神经球(BMSC-NSs)移植是否会对恢复产生协同作用。材料与方法:成年Sprague-Dawley大鼠在T10椎骨水平受到脊髓损伤(SCI)。损伤后,立即鞘内给予NEP1-40大鼠4周。 SCI后7天,将BrdU标记的BMSC-NS(2x105)移植到受伤部位。用BBB评分评估运动恢复10周。挫伤后10周对动物进行心内灌注,并进行组织学检查。结果:在挫伤7周时,联合治疗组的运动恢复明显优于对照组。两种单药治疗均未改善运动功能。联合治疗组的胆囊腔平均面积明显小于对照组。荧光显微镜分析表明,NEP1-40显着抑制了神经胶质瘢痕的形成,并促进了轴突渗透到瘢痕屏障中。结论:这项研究表明,BMSC-NSs和NEP 1-40对大鼠SCI的恢复具有协同作用。这可能代表了治疗SCI的潜在新策略。

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