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首页> 外文期刊>Neuropsychiatric Disease and Treatment >Electroacupuncture Promoting Axonal Regeneration in Spinal Cord Injury Rats via Suppression of Nogo/NgR and Rho/ROCK Signaling Pathway
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Electroacupuncture Promoting Axonal Regeneration in Spinal Cord Injury Rats via Suppression of Nogo/NgR and Rho/ROCK Signaling Pathway

机译:通过抑制Nogo / Ngr和Rho /岩石信号通路抑制脊髓损伤大鼠轴突再生的电针

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摘要

Purpose: To observe the changes of Nogo/NgR and Rho/ROCK signaling pathway-related gene and protein expression in rats with spinal cord injury (SCI) treated with electroacupuncture (EA) and to further investigate the possible mechanism of EA for treating SCI. Methods: Allen’s method was used to create the SCI rat model. Sixty-four model rats were further subdivided into four subgroups, namely, the SCI model group (SCI), EA treatment group (EA), blocking agent Y27632 treatment group (Y27632) and EA+blocking agent Y27632 treatment group (EA+Y), according to the treatment received. The rats were subjected to EA and/or blocking agent Y27632 treatment. After 14 days, injured spinal cord tissue was extracted for analysis. The mRNA and protein expression levels were determined by real-time fluorescence quantitative PCR and Western blotting, respectively. Cell apoptosis changes in the spinal cord were evaluated by in situ hybridization. Hindlimb motor function in the rats was evaluated by Basso-Beattie-Bresnahan assessment methods. Results: Except for RhoA protein expression, compared with the SCI model group, EA, blocking agent Y27632 and EA+blocking agent Y27632 treatment groups had significantly reduced mRNA and protein expression of Nogo-A, NgR, LINGO-1, RhoA and ROCK II in spinal cord tissues, increased mRNA and protein expression of MLCP, decreased p-MYPT1 protein expression and p-MYPT1/MYPT1 ratio, and caspase3 expression, and improved lower limb movement function after treatment for 14 days (P0.01 or 0.05). The combination?of EA and the blocking agent Y27632 was superior to EA or blocking agent Y27632 treatment alone (P 0.01 or 0.05). Conclusion: EA may have an obvious inhibitory effect on the Nogo/NgR and Rho/ROCK signaling pathway after SCI, thereby reducing the inhibition of axonal growth, which may be a key mechanism of EA treatment for SCI.
机译:目的:观察用电针(EA)处理的脊髓损伤(SCI)对大鼠Nogo / NgR和Rho /摇滚信令途径相关基因和蛋白质表达,进一步研究EA治疗SCI的可能机制。方法:Allen的方法用于创建SCI大鼠模型。六十四种模型大鼠进一步细分为四个亚组,即SCI模型组(SCI),EA治疗组(EA),阻断剂Y27632处理组(Y27632)和EA +阻断剂Y27632治疗组(EA + Y) ,根据收到的治疗。对大鼠进行EA和/或阻断剂Y27632处理。 14天后,提取受伤的脊髓组织进行分析。通过实时荧光定量PCR和Western印迹测定mRNA和蛋白表达水平。通过原位杂交评估脊髓细胞凋亡的变化。大鼠中的后肢电机功能由Basso-Beattie-Bresnahan评估方法评估。结果:除了rhOA蛋白表达外,与SCI模型组相比,EA,阻断剂Y27632和EA +阻断剂Y27632治疗组具有显着降低的MRNA-A,NGR,Lingo-1,RhoA和岩石II的mRNA和蛋白表达在脊髓组织中,MLCP的增加的mRNA和蛋白质表达,降低P-mypt1蛋白表达和P-mypt1 / mypt1的比例,并且Caspase3表达,并在治疗后改善了下肢运动功能14天(P <0.01或<0.05) 。组合α和阻断剂Y27632优于EA或阻断剂Y27632单独处理(P <0.01或<0.05)。结论:SCI后对Nogo / NgR和Rho /岩石信号通路具有明显的抑制作用,从而降低了轴突生长的抑制,这可能是SCI的EA治疗的关键机制。

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