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首页> 外文期刊>Journal of neurotrauma >Attenuation of the electrophysiological function of the corpus callosum after fluid percussion injury in the rat.
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Attenuation of the electrophysiological function of the corpus callosum after fluid percussion injury in the rat.

机译:大鼠液压冲击损伤后call体的电生理功能减弱。

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This study describes a new method used to evaluate axonal physiological dysfunction following fluid percussion induced traumatic brain injury (TBI) that may facilitate the study of the mechanisms and novel therapeutic strategies of posttraumatic diffuse axonal injury (DAI). Stimulated compound action potentials (CAP) were recorded extracellularly in the corpus callosum of superfused brain slices at 3 h, and 1, 3, and 7 days following central fluid percussion injury and demonstrated a temporal pattern of functional deterioration. The maximal CAP amplitude (CAPA) covaried with the intensity of impact 1 day following sham, mild (1.0-1.2 atm), and moderate (1.8-2.0 atm) injury (p < 0.05; 1.11 +/- 0.10, 0.82 +/- 0.11, and 0.49 +/- 0.08 mV, respectively). The CAPA in sham animals were approximately 1.1 mV and did not vary with survival interval (3 h, and 1, 3, and 7 days); however, they were significantly decreased at each time point following moderate injury (p < 0.05; 0.51 +/- 0.11, 0.49 +/- 0.08, 0.46 +/- 0.10, and 0.75 +/- 0.13 mV, respectively). The CAPA at 7 days in the injured group were higher than at 3 h, and 1 and 3 days. H&E and amyloid precursor protein (APP) light microscopic analysis confirmed previously reported trauma-induced axonal injury in the corpus callosum seen after fluid percussion injury. Increased APP expression was confirmed using Western blotting showing significant accumulation at 1 day (IOD 913.0 +/- 252.7; n = 3; p = 0.05), 3 days (IOD 753.1 +/- 159.1; n = 3; p = 0.03), and at 7 days (IOD 1093.8 = 105.0; n = 3; p = 0.001) compared to shams (IOD 217.6 +/- 20.4; n = 3). Thus, we report the characterization of white matter axonal dysfunction in the corpus callosum following TBI. This novel method was easily applied, and the results were consistent and reproducible. The electrophysiological changes were sensitive to the early effects of impact intensity, as well as to delayed changes occurring several days following injury. They also indicated a greater degree of attenuation than predicted by APP expression changes alone.
机译:这项研究描述了一种新的方法,用于评估液压冲击引起的颅脑损伤(TBI)后的轴突生理功能障碍,这可能有助于研究创伤后弥漫性轴索损伤(DAI)的机制和新的治疗策略。在中央液体撞击伤后3小时,1、3和7天,在融合脑片的call体的细胞外记录了刺激的复合动作电位(CAP)。假性,轻度(1.0-1.2 atm)和中度(1.8-2.0 atm)损伤后1天的最大CAP振幅(CAPA)与撞击强度相关(p <0.05; 1.11 +/- 0.10,0.82 +/-分别为0.11和0.49 +/- 0.08 mV)。假动物的CAPA约为1.1 mV,并且没有随生存间隔(3 h,1、3和7天)而变化;但是,它们在中度损伤后的每个时间点均显着降低(分别为p <0.05; 0.51 +/- 0.11、0.49 +/- 0.08、0.46 +/- 0.10和0.75 +/- 0.13 mV)。受伤组中第7天的CAPA高于3小时,第1天和第3天。 H&E和淀粉样蛋白前体蛋白(APP)的光学显微镜分析证实了先前报道的液体撞击伤后创伤引起的trauma体轴突损伤。使用Western印迹证实APP表达增加,显示在1天(IOD 913.0 +/- 252.7; n = 3; p = 0.05),3天(IOD 753.1 +/- 159.1; n = 3; p = 0.03)有明显的积累,与第7天(IOD 217.6 +/- 20.4; n = 3)相比,第7天(IOD 1093.8 = 105.0; n = 3; p = 0.001)。因此,我们报告了TBI后call体中白质轴突功能障碍的特征。这种新颖的方法易于应用,结果一致且可重复。电生理变化对冲击强度的早期影响以及受伤后几天发生的延迟变化很敏感。他们还指出,衰减程度要比仅通过APP表达变化所预测的程度更大。

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