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首页> 外文期刊>Journal of reconstructive microsurgery >Chronic Nerve Compression Accelerates the Progression of Diabetic Peripheral Neuropathy in a Rat Model: A Study of Gene Expression Profiling
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Chronic Nerve Compression Accelerates the Progression of Diabetic Peripheral Neuropathy in a Rat Model: A Study of Gene Expression Profiling

机译:慢性神经压缩加速了大鼠模型中糖尿病外周神经病变的进展:基因表达分析研究

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Objective This article investigates the role of chronic nerve compression in the progression of diabetic peripheral neuropathy (DPN) by gene expression profiling. Methods Chronic nerve compression was created in streptozotocin (STZ)-induced diabetic rats by wrapping a silicone tube around the sciatic nerve (SCN). Neurological deficits were evaluated using pain threshold test, motor nerve conduction velocity (MNCV), and histopathologic examination. Differentially expressed genes (DGEs) and metabolic processes associated with chronic nerve compression were analyzed. Results Significant changes in withdrawal threshold and MNCV were observed in diabetic rats 6 weeks after diabetes induction, and in DPN rats 4 weeks after diabetes induction. Histopathologic examination of the SCN in DPN rats presented typical changes of myelin degeneration in DPN. Function analyses of DEGs demonstrated that biological processes related to inflammatory response, extracellular matrix component, and synaptic transmission were upregulated after diabetes induction, and chronic nerve compression further enhanced those changes. While processes related to lipid and glucose metabolism, response to insulin, and apoptosis regulation were inhibited after diabetes induction, chronic nerve compression further enhanced these inhibitions. Conclusion Our study suggests that additional silicone tube wrapping on the SCN of rat with diabetes closely mimics the course and pathologic findings of human DPN. Further studies are needed to verify the effectiveness of this rat model of DPN and elucidate the roles of the individual genes in the progression of DPN.
机译:目的本文通过基因表达分析研究了慢性神经压缩在糖尿病外周神经病变(DPN)进展中的作用。方法通过在坐骨神经(SCN)周围缠绕硅氧烷管,在链脲佐菌素(STZ)诱导糖尿病大鼠中产生慢性神经压缩。使用疼痛阈值测试,运动神经传导速度(MNCV)和组织病理学检查来评估神经系统缺陷。分析了与慢性神经压缩相关的差异表达的基因(蒸频)和代谢过程。结果糖尿病诱导后6周和糖尿病诱导后4周的DPN大鼠在糖尿病大鼠和DPN大鼠中观察到退出阈值和MNCV的显着变化。 DPN大鼠SCN的组织病理学检查介绍了DPN中髓鞘变性的典型变化。 Degs的功能分析证明,糖尿病诱导后上调了与炎症反应,细胞外基质组分和突触传递有关的生物过程,慢性神经压缩进一步增强了这些变化。虽然糖尿病诱导术后抑制与脂质和葡萄糖代谢的过程,对胰岛素的反应和凋亡调节抑制,但慢性神经压缩进一步提高了这些抑制作用。结论我们的研究表明,患有糖尿病大鼠SCN的额外有机硅管紧密模仿人DPN的过程和病理发现。需要进一步的研究来验证DPN大鼠模型的有效性,并阐明单个基因在DPN进展中的作用。

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