Department of Orthopedics, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Neurol India. 2011 Jul-Aug;59(4):579-85. doi: 10.4103/0028-3886.84341.
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.
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 (2×105 ) 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.
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.
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.
研究表明,给予 Nogo-66 受体拮抗剂肽 NEP1-40 可改善大鼠的运动功能恢复。我们假设,将 NEP1-40 与另一种有前途的治疗方法——神经干细胞移植相结合,可能会进一步提高运动功能恢复的程度。在本研究中,我们研究了 NEP1-40 与骨髓基质细胞源性神经球(BMSC-NSs)移植相结合是否会产生协同作用。
成年 Sprague-Dawley 大鼠在 T10 椎骨水平进行脊髓损伤(SCI)。损伤后立即鞘内给予 NEP1-40 4 周。SCI 后 7 天,将 BrdU 标记的 BMSC-NSs(2×105 个)移植到损伤部位。用 BBB 评分评估 10 周的运动功能恢复情况。在挫伤后 10 周,经心灌注动物,进行组织学检查。
与对照组相比,联合治疗组在挫伤后 7 周时的运动恢复有显著统计学差异。两种单药治疗均未改善运动功能。联合治疗组的囊腔平均面积明显小于对照组。荧光显微镜分析表明,NEP1-40 可显著抑制胶质瘢痕的形成,并促进轴突穿透瘢痕屏障。
本研究表明,BMSC-NSs 和 NEP1-40 对大鼠 SCI 的恢复具有协同作用。这可能代表 SCI 治疗的一种新的潜在策略。