Bamba Ravinder, Riley David Colton, Kim Justine S, Cardwell Nancy L, Pollins Alonda C, Shack R Bruce, Thayer Wesley P
Department of Plastic Surgery, Vanderbilt University Medical Center, Nashville, TN; Department of Surgery, Georgetown University, Washington, DC.
Department of Plastic Surgery, Vanderbilt University Medical Center, Nashville, TN; Georgetown University School of Medicine, Washington, DC.
J Hand Surg Am. 2018 Jan;43(1):82.e1-82.e7. doi: 10.1016/j.jhsa.2017.07.014. Epub 2017 Aug 16.
Polyethylene glycol (PEG) has been hypothesized to restore axonal continuity using an in vivo rat sciatic nerve injury model when nerve repair occurs within minutes after nerve injury. We hypothesized that PEG could restore axonal continuity when nerve repair was delayed.
The left sciatic nerves of female Sprague-Dawley rats were transected and repaired in an end-to-end fashion using standard microsurgical techniques at 3 time points (1, 8, and 24 hours) after injury. Polyethylene glycol was delivered to the neurorrhaphy in the experimental group. Post-repair compound action potentials were immediately recorded after repair. Animals underwent behavioral assessments at 3 days and 1 week after surgery using the sciatic functional index test. The animals were sacrificed at 1 week to obtain axon counts.
The PEG-treated nerves had improved compound action potential conduction and animals treated with PEG had improved sciatic function index. Compound action potential conduction was restored in PEG-fused rats when nerves were repaired at 1, 8, and 24 hours. In the control groups, no compound action potential conduction was restored when nerves were repaired. Sciatic functional index was superior in PEG-fused rats at 3 and 7 days after surgery compared with control groups at all 3 time points of nerve repair. Distal motor and sensory axon counts were higher in the PEG-treated rats.
Polyethylene glycol fusion is a new adjunct for nerve repair that allows rapid restoration of axonal continuity. It effective when delayed nerve repair is performed.
Nerve repair with application of PEG is a potential therapy that may have efficacy in a clinical setting. It is an experimental therapy that needs more investigation as well as clinical trials.
有人提出,在大鼠坐骨神经损伤模型中,当神经损伤后数分钟内进行神经修复时,聚乙二醇(PEG)可恢复轴突的连续性。我们推测,当神经修复延迟时,PEG仍可恢复轴突的连续性。
对雌性Sprague-Dawley大鼠的左侧坐骨神经进行横断,并在损伤后的3个时间点(1、8和24小时)使用标准显微外科技术进行端端修复。在实验组中,将聚乙二醇应用于神经缝合处。修复后立即记录复合动作电位。术后3天和1周,使用坐骨神经功能指数测试对动物进行行为评估。术后1周处死动物以进行轴突计数。
经PEG处理的神经,其复合动作电位传导得到改善,接受PEG治疗的动物坐骨神经功能指数也有所提高。当在1、8和24小时进行神经修复时,PEG融合的大鼠恢复了复合动作电位传导。在对照组中,神经修复后未恢复复合动作电位传导。与所有3个神经修复时间点的对照组相比,PEG融合的大鼠在术后3天和7天的坐骨神经功能指数更高。PEG治疗组大鼠的远端运动和感觉轴突计数更高。
聚乙二醇融合是一种用于神经修复的新辅助方法,可快速恢复轴突的连续性。在进行延迟神经修复时有效。
应用PEG进行神经修复是一种可能在临床环境中有效的潜在治疗方法。这是一种需要更多研究以及临床试验的实验性治疗方法。