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骨髓基质细胞与 Rho 激酶(ROCK)抑制剂法舒地尔协同促进大鼠脊髓损伤轴突再生。

Synergistic effects of bone marrow stromal cells and a Rho kinase (ROCK) inhibitor, fasudil on axon regeneration in rat spinal cord injury.

机构信息

Department of Neurosurgery, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

出版信息

Neuropathology. 2010 Jun;30(3):241-50. doi: 10.1111/j.1440-1789.2009.01077.x. Epub 2009 Nov 18.

Abstract

Transplanted bone marrow stromal cells (BMSC) promote functional recovery after spinal cord injury (SCI) through multiple mechanisms. A Rho kinase inhibitor, Fasudil also enhances axonal regeneration. This study was aimed to evaluate whether combination therapy of BMSC transplantation and Fasudil further enhances axonal regeneration and functional recovery in rats subjected to SCI. Fasudil or vehicle was injected for 2 weeks. BMSC or vehicle transplantation into the rostral site of SCI was performed at 7 days after injury. Neurological symptoms were assessed throughout the experiments. Fluoro-Ruby was injected into the dorsal funiculus of the rostral site of SCI at 63 days after injury. The fate of the transplanted BMSC was examined using immunohistochemistry. BMSC transplantation significantly increased the number of Fluoro-Ruby -labeled fibers of the dorsal corticospinal tracts at the caudal site of SCI, enhancing functional recovery of the hind limbs. Some of the engrafted BMSC were positive for Fluoro-Ruby, neuronal specific nuclear protein and microtubule-associated protein-2, suggesting that they acquired neuronal phenotypes and built synaptic connection with the host's neural circuits. Fasudil treatment also improved axonal continuity, but did not promote functional recovery. Combination therapy dramatically increased the number of Fluoro-Ruby-labeled fibers of the dorsal corticospinal tracts at the caudal site of SCI, but did not further boost the therapeutic effects on locomotor function by BMSC transplantation. The findings suggest that BMSC transplantation and Fasudil provide synergistic effects on axon regeneration after SCI, although further studies would be necessary to further enhance functional recovery.

摘要

骨髓基质细胞(BMSC)通过多种机制促进脊髓损伤(SCI)后的功能恢复。Rho 激酶抑制剂法舒地尔也能促进轴突再生。本研究旨在评估 BMSC 移植和法舒地尔联合治疗是否能进一步增强 SCI 大鼠的轴突再生和功能恢复。在损伤后 7 天,Fasudil 或载体注射 2 周,BMSC 或载体移植到 SCI 的近端部位。在整个实验过程中评估神经症状。在损伤后 63 天,将荧光 Ruby 注入 SCI 近端背柱。用免疫组织化学法检查移植 BMSC 的命运。BMSC 移植显著增加了 SCI 尾部背侧皮质脊髓束中 Fluoro-Ruby 标记纤维的数量,增强了后肢的功能恢复。一些植入的 BMSC 对 Fluoro-Ruby、神经元特异性核蛋白和微管相关蛋白-2 呈阳性,表明它们获得了神经元表型,并与宿主的神经回路建立了突触连接。Fasudil 治疗也改善了轴突连续性,但没有促进功能恢复。联合治疗显著增加了 SCI 尾部背侧皮质脊髓束中 Fluoro-Ruby 标记纤维的数量,但并没有进一步增强 BMSC 移植对运动功能的治疗效果。研究结果表明,BMSC 移植和法舒地尔对 SCI 后轴突再生有协同作用,尽管需要进一步研究以进一步增强功能恢复。

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