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Establishment of a Spinal Cord Injury Model in Adult Rats by an Electrocircuit-Controlled Impacting Device and its Pathological Observations

机译:电路控制冲击装置在成年大鼠脊髓损伤模型中的建立及病理观察

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One of the crucial challenges in medicine is the treatment and rehabilitation of spinal cord injury (SCI). In this study, we established a stable and reproducible acute spinal cord injury model in adult rats. The SCI was inflicted by our self-innovated spinal cord impact device controlled by electrical circuit. The Basso, Beattie, and Bresnahan Locomotor Rating Scale (BBB) score, electrophysiology, histological, and immunohistochemical changes after SCI were observed. The BBB score of the injured rats began to increase from the 3rd day of SCI and reached at the score 7.2 ± 1.3 at the 28th day. The latency of cortical somatosensory evoked potentials (CSEP) was not observed 2 and 6 h after injury, but appeared 24 h after injury which was significantly prolonged. It recovered from day 3 gradually to 27.3 ± 2.7 ms on day 28. H&E staining showed that the structure of gray and white matter was disrupted after the SCI. The result also showed dramatic neuron degenerations, cellular swelling, and the proliferation of glial cells. The immunohistochemical analysis showed that the expression of neuron specific enolase (NSE) and neurofilament 200 (NF200) started lowering at 2 h and dropped to the bottom at 24 h. Their expression rebound from day 3 and yet to the original level at day 28 (P < 0.05). The number of cells expressing glial fibrillary acidic protein (GFAP) hiked from day 3, peaked at day 14, and began recovering from day 28 (P < 0.05). The changes of NSE, NF200, GFAP, and CSEP were significantly associated with the BBB score (P < 0.05). In conclusion, our self-innovated device can reproduce the injury model stably. The changes of NSE, NF, and GFAP after spinal cord injury reflect the characteristics of pathological change, which are closely associated with the functional recovery from the spinal cord injury.
机译:医学上的关键挑战之一是脊髓损伤(SCI)的治疗和康复。在这项研究中,我们建立了成年大鼠稳定和可复制的急性脊髓损伤模型。 SCI是由我们通过电路控制的自主创新的脊髓撞击装置造成的。观察到SCI后的Basso,Beattie和Bresnahan运动自评量表(BBB)得分,电生理,组织学和免疫组化变化。受伤大鼠的BBB评分从SCI第3天开始增加,并在第28天达到7.2±1.3。损伤后2和6小时未观察到皮层体感诱发电位(CSEP)的潜伏期,但在损伤后24小时出现潜伏期,这显着延长。它从第3天开始逐渐恢复至第28天的27.3±2.7ms。H&E染色显示SCI后灰色和白色物质的结构被破坏。结果还显示出严重的神经元变性,细胞肿胀和神经胶质细胞的增殖。免疫组织化学分析显示,神经元特异性烯醇化酶(NSE)和神经丝200(NF200)的表达在2 h开始降低,在24 h降至底部。他们的表达从第3天开始反弹,但到第28天仍恢复到原始水平(P <0.05)。从第3天开始,表达神经胶质纤维酸性蛋白(GFAP)的细胞数量增加,在第14天达到峰值,并从第28天开始恢复(P <0.05)。 NSE,NF200,GFAP和CSEP的变化与BBB评分显着相关(P <0.05)。总之,我们的创新设备可以稳定地再现损伤模型。脊髓损伤后NSE,NF和GFAP的变化反映了病理变化的特征,这与脊髓损伤后的功能恢复密切相关。

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