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4-氨基吡啶用于慢性脊髓损伤患者的临床前试验。

Preclinical trial of 4-aminopyridine in patients with chronic spinal cord injury.

作者信息

Hayes K C, Blight A R, Potter P J, Allatt R D, Hsieh J T, Wolfe D L, Lam S, Hamilton J T

机构信息

Department of Physical Medicine & Rehabilitation, Parkwood Hospital, London, Ontario, Canada.

出版信息

Paraplegia. 1993 Apr;31(4):216-24. doi: 10.1038/sc.1993.40.

Abstract

4-Aminopyridine (4-AP) is a K+ channel blocking agent that enhances nerve conduction through areas of demyelination by prolonging the duration of the action potential and increasing the safety factor for conduction. We have investigated the effects of 4-AP (24 mg total dose-intravenous) in 6 patients with spinal cord injury (3 complete, 3 incomplete) with the intent of overcoming central conduction block, or slowing, due to demyelination. Vital signs remained stable and only mild side effects were noted. The 3 patients with incomplete injuries all demonstrated enhanced volitional EMG interference patterns and one patient exhibited restored toe movements. The changes were reversed on drug washout. There were no changes in segmental reflex activities. These results are consistent with those obtained from 4-AP trials with animal models of spinal cord injury, showing modest therapeutic benefit attributable to enhanced central conduction.

摘要

4-氨基吡啶(4-AP)是一种钾通道阻滞剂,它通过延长动作电位的持续时间和增加传导的安全系数来增强神经在脱髓鞘区域的传导。我们研究了4-AP(总剂量24毫克,静脉注射)对6例脊髓损伤患者(3例完全性损伤,3例不完全性损伤)的影响,目的是克服因脱髓鞘导致的中枢传导阻滞或传导减慢。生命体征保持稳定,仅观察到轻微的副作用。3例不完全性损伤患者的随意肌电图干扰模式均增强,1例患者的脚趾运动恢复。停药后这些变化逆转。节段性反射活动无变化。这些结果与在脊髓损伤动物模型上进行的4-AP试验结果一致,表明因中枢传导增强而有适度的治疗益处。

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