实验性脊髓损伤大鼠的治疗模型:1 .死亡率和运动障碍。

P L Perot, W A Lee, C Y Hsu, E L Hogan, R D Cox, A J Gross
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引用次数: 46

摘要

在建立实验性脊髓损伤大鼠治疗模型的过程中,我们测定了外伤剂量(20、30、40、50和60 g-cm)对损伤后4周死亡率和运动功能障碍的影响。死亡率与创伤剂量有关:20 g-cm, 11%;30 g-cm, 14%;40 g-cm, 27%;50 g-cm, 32%;60 g-cm, 41%。线性回归的统计分析表明,死亡率随创伤剂量的增加而增加。由改良的Tarlov量表测定的运动缺陷也依赖于创伤剂量。基于本研究的创伤剂量-反应曲线表明,如果安慰剂组和治疗组各有30只大鼠,则可以检测到将运动缺陷从40 g-cm减少到30 g-cm的药物,其显著水平为0.05,幂为0.8。同样的样本量将发现死亡率从40 g-cm显著降低到30 g-cm。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic model for experimental spinal cord injury in the rat: I. Mortality and motor deficit.

In the course of establishing a therapeutic model for experimental spinal cord injury in the rat, we determined the effects of trauma dose (20, 30, 40, 50, and 60 g-cm) on the mortality and motor deficit in the 4 weeks following injury. Mortality was dependent upon the trauma dose: 20 g-cm, 11%; 30 g-cm, 14%; 40 g-cm, 27%; 50 g-cm, 32%; 60 g-cm, 41%. Statistical analysis by linear regression is highly significant for increasing mortality with increasing trauma dose. The motor deficit determined by a modified Tarlov scale also was dependent upon trauma dose. A trauma dose-response curve based on this study indicates that a drug which reduces the motor deficit from that found at 40 g-cm to that at 30 g-cm may be detected at a significant level of 0.05 with a power of 0.8 if 30 rats are included in each of placebo and treated groups. The same sample size would detect a significant reduction of mortality from that of 40 g-cm to 30 g-cm.

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