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重组人促红细胞生成素可预防大鼠慢性颈脊髓压迫模型中运动神经元凋亡。

Recombinant human erythropoietin prevents motor neuron apoptosis in a rat model of cervical sub-acute spinal cord compression.

机构信息

Shandong University, Shandong, China; Department of Orthopedic, Jinan Central Hospital of Shandong University, Shandong, China.

出版信息

Neurosci Lett. 2011 Feb 18;490(1):57-62. doi: 10.1016/j.neulet.2010.12.025. Epub 2010 Dec 16.

Abstract

The objective of the study was to investigate the effects of recombinant human erythropoietin (rhEPO) in a rat model of cervical sub-acute spinal cord compression. 80 Wistar rats were randomly divided into 4 groups. Rats in the sham group (Group A, n=5) underwent surgical procedures without cervical spinal cord compression; while rats in other groups were subjected to the spinal compression process. In the control group (Group B, n=25), rats received an i.v. injection of 1 mL saline at day 7 post-surgery. Rats in the low-dose group (Group C, n=25) and the high-dose group (Group D, n=25) were treated with rhEPO at 500 units/kg body-weight and 5000 units/kg, respectively, via intravenous injection at day 7 post surgery. Limb motor function was scored by Basso-Beattie-Bresnahan (BBB) standards at 3, 7, 14, 21 and 28 days post-surgery. The distribution and quantities of EPO and its receptor (EPO-R) in the compressed segment of the spinal cord were detected by immunohistochemistry. Motor neuron apoptosis in the spinal cord was evaluated using TUNEL staining and flow cytometry at the indicated time points. Finally, IL-8, TNF-α, IL-6, and IL-1β levels in the compressed cervical spinal cord were determined by ELISA within the lesion epicenter at each time point post-surgery. The data suggest that expression of EPO-R was significantly increased following sub-acute cervical spinal cord compression; Groups C and D exhibited better BBB scores at all observed time points compared with the control group (p<0.01). Using TUNEL staining and FCM, we observed that rhEPO profoundly inhibited motor neuron apoptosis in the spinal cord at day 21 (p<0.01). Additionally, treatment with rhEPO halted the elevation of inflammatory cytokines. rhEPO administration decreased motor neuron apoptosis in the cervical spinal cord, improved motor functions and reduced the inflammatory response in a sub-acute cervical spinal cord compression model. Moreover, sustained treatment with low doses of rhEPO revealed a positive therapeutic effect.

摘要

本研究旨在探讨重组人促红细胞生成素(rhEPO)在大鼠慢性颈脊髓压迫模型中的作用。80 只 Wistar 大鼠随机分为 4 组。假手术组(A 组,n=5)大鼠行手术但不压迫颈脊髓;其余各组大鼠行脊髓压迫手术。对照组(B 组,n=25)大鼠术后第 7 天给予静脉注射生理盐水 1ml。低剂量组(C 组,n=25)和高剂量组(D 组,n=25)大鼠分别于术后第 7 天给予 rhEPO500 单位/kg 和 5000 单位/kg 静脉注射。术后第 3、7、14、21 和 28 天采用 Basso-Beattie-Bresnahan(BBB)评分标准评估大鼠肢体运动功能。免疫组化法检测受压脊髓段 EPO 及其受体(EPO-R)的分布和数量。在指定时间点采用 TUNEL 染色和流式细胞术评估脊髓运动神经元凋亡。最后,在术后各时间点,采用 ELISA 法测定病变中心受压颈脊髓 IL-8、TNF-α、IL-6 和 IL-1β 水平。结果显示,慢性颈脊髓压迫后 EPO-R 表达明显增加;与对照组相比,C 组和 D 组在所有观察时间点的 BBB 评分均明显升高(p<0.01)。TUNEL 染色和 FCM 结果显示,rhEPO 可显著抑制脊髓运动神经元在第 21 天的凋亡(p<0.01)。此外,rhEPO 治疗可阻止炎症细胞因子水平升高。rhEPO 可减少慢性颈脊髓压迫模型中脊髓运动神经元凋亡,改善运动功能,减轻炎症反应,且持续低剂量 rhEPO 治疗具有积极的治疗效果。

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