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首页> 外文期刊>International Journal of Neuroscience >The effects of triptolide on the cellular activity of cryopreserved rat sciatic nerves and nerve regeneration after allotransplantation
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The effects of triptolide on the cellular activity of cryopreserved rat sciatic nerves and nerve regeneration after allotransplantation

机译:ringolide对冷冻保存大鼠坐骨神经和神经再生后的细胞活性的影响

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摘要

Purpose: To investigate the effects of triptolide (T10) on the cellular activity of cryopreserved rat sciatic nerves and nerve regeneration after allotransplantation. Materials and methods: After the optimal T10 concentration was determine, sciatic nerve fragments from Sprague-Dawley (SD) rats were randomly divided into 5 groups: the fresh nerve group (group A), the Dulbecco's modified Eagle's medium (DMEM)-preservation group (group B), the T10-preservation group (group C), the T10-pretreatment, DMEM-preservation group (group D), and the T10-pretreatment, T10-preservation group (group E). The nerves in the preservation groups were preserved at 4 degrees C for 4 w. Then, either cryopreserved or fresh nerves were used to repair 10-mm sciatic nerve defects in Wistar rats (group A ', group B ', group C ', group D ', and group E ', which correspond to the nerve groups described above); in addition, one fresh homologous transplantation group (group F ') was established. Results: Nerve growth factor (NGF) was expressed at significantly higher levels in the groups treated with the T10 solution at 37 degrees C. After rat sciatic nerves were cryopreserved for 4 w, group E had increased numbers of live nerve cells and increased levels of biological activity (P < 0.001) and reduced levels of immunogenicity (P < 0.001) when compared with those for the other groups. Sixteen weeks after transplantation, recipient nerve regeneration in group E ' was increased compared with that in groups A ', B ', C ', and D ' (P < 0.05). Conclusions: The application of T10 in vitro induced the expression of neurotrophic factors in rat sciatic nerves, increased the biological activity of cryopreserved nerves, reduced immunogenicity, and promoted recipient nerve regeneration after allotransplantation.
机译:目的:探讨雷公藤内酯(T10)对分征后冷冻保存大鼠坐骨神经和神经再生的细胞活性的影响。材料和方法:在最佳T10浓度确定后,来自Sprague-Dawley(SD)大鼠的坐骨神经碎片随机分为5组:新鲜神经组(A组),Dulbecco改良的Eagle的培养基(DMEM) - 营业组(B组),T10保存组(C组),T10-PRETREATEMMENT,DMEM保存组(D)和T10-PRETREATMENT,T10-PRETERATION组(e)。保存组中的神经以4℃保存4次。然后,使用冷冻保存或新鲜神经来修复Wistar大鼠(A',B组,C组,组和e'组D'和Group e'中的10mm坐骨神经缺陷,其对应于上述神经基团);此外,建立了一种新鲜同源移植组(组F')。结果:神经生长因子(NGF)在37℃下用T10溶液处理的基团的显着较高的水平表达。在对大鼠坐骨神经中冷却4W后,e群次数增加了活神经细胞数量和增加的水平与其他组相比,生物活性(P <0.001)和免疫原性水平降低(P <0.001)。移植后十六周,e'组中的受体神经再生与A',B',C'和D'组(P <0.05)增加。结论:T10在体外应用诱导大鼠坐骨神经中神经营养因子的表达,增加了冷冻保存神经的生物活性,降低免疫原性,并在同质化后促进受体神经再生。

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