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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >The Effect of Electroacupuncture on the Extracellular Matrix Synthesis and Degradation in a Rabbit Model of Disc Degeneration
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The Effect of Electroacupuncture on the Extracellular Matrix Synthesis and Degradation in a Rabbit Model of Disc Degeneration

机译:电针对家兔椎间盘退变模型细胞外基质合成与降解的影响。

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The present study was aimed at determining if the electroacupuncture (EA) is able to protect degenerated disc in vivo. New Zealand white rabbits (n = 40) were used for the study. The rabbits were randomly assigned to four groups. EA intervention was applied to one of the four groups. Magnetic resonance imaging and Pfirrmann's classification were obtained for each group to evaluate EA treatment on the intervertebral disc degeneration. Discs were analyzed using immunofluorescence for the labeling of collagens 1 and 2, bone morphogenetic protein-2 (BMP-2), matrix metalloproteinase-13 (MMP-13), and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1). For protein expression analysis, western blot was used for biglycan and decorin. Outcomes indicated that EA intervention decreased the grades compared with the compressed disc. Immunofluorescence analysis showed a significant increase of collagens 1 and 2, TIMP-1, and BMP-2 positive cells, in contrast to MMP-13 after EA treatment for 28 days. The protein expression showed a sign of regeneration that decorin and biglycan were upregulated. It was concluded that EA contributed to the extracellular matrix (ECM) anabolic processes and increased the ECM components. MMPs and their inhibitors involved in the mechanism of EA intervention on ECM decreased disc. It kept a dynamic balance between ECM synthesis and degradation.
机译:本研究旨在确定电针(EA)是否能够在体内保护退化的椎间盘。该研究使用了新西兰白兔(n = 40)。将兔子随机分为四组。 EA干预应用于四组之一。每组均获得磁共振成像和Pfirrmann分类,以评估EA对椎间盘退变的治疗效果。使用免疫荧光对椎间盘进行分析,以标记胶原蛋白1和2,骨形态发生蛋白2(BMP-2),基质金属蛋白酶13(MMP-13)和组织金属蛋白酶-1组织抑制剂(TIMP-1)。对于蛋白质表达分析,蛋白质印迹用于双糖链蛋白聚糖和decorin。结果表明,与压缩椎间盘相比,EA干预降低了评分。免疫荧光分析显示,与EA处理28天后的MMP-13相比,胶原1和2,TIMP-1和BMP-2阳性细胞显着增加。蛋白质表达显示出再生的迹象,即decorin和biglycan被上调。结论是,EA促进了细胞外基质(ECM)的合成代谢过程并增加了ECM成分。 MMP及其抑制剂参与EA对ECM的干预机制降低了椎间盘。它在ECM合成和降解之间保持了动态平衡。

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