Riley David Colton, Boyer Richard B, Deister Curt A, Pollins Alonda C, Cardwell Nancy L, Kelm Nathaniel D, Does Mark D, Dortch Richard D, Bamba Ravinder, Shack Robert Bruce, Thayer Wesley P
From the *Department of Plastic Surgery, Vanderbilt University Medical Center, Nashville, TN; †Axogen Corporation, Alachua, FL; ‡Vanderbilt University Institute of Imaging Science; and §Department of Radiology and Radiological Sciences, Vanderbilt University, Nashville, TN.
Ann Plast Surg. 2017 Dec;79(6):590-599. doi: 10.1097/SAP.0000000000001242.
The management of peripheral nerve injuries remains a large challenge for plastic surgeons. With the inability to fuse axonal endings, results after microsurgical nerve repair have been inconsistent. Our current nerve repair strategies rely upon the slow and lengthy process of axonal regeneration (~1 mm/d). Polyethylene glycol (PEG) has been investigated as a potential axonal fusion agent; however, the percentage of axonal fusion has been inconsistent. The purpose of this study was to identify a PEG delivery device to standardize outcomes after attempted axonal fusion with PEG.
We used a rat sciatic nerve injury model in which we completely transected and repaired the left sciatic nerve to evaluate the efficacy of PEG fusion over a span of 12 weeks. In addition, we evaluated the effectiveness of a delivery device's ability to optimize results after PEG fusion.
We found that PEG rapidly (within minutes) restores axonal continuity as assessed by electrophysiology, fluorescent retrograde tracer, and diffusion tensor imaging. Immunohistochemical analysis shows that motor axon counts are significantly increased at 1 week, 4 weeks, and 12 weeks postoperatively in PEG-treated animals. Furthermore, PEG restored behavioral functions up to 50% compared with animals that received the criterion standard epineurial repair (control animals).
The ability of PEG to rapidly restore nerve function after neurotmesis could have vast implications on the clinical management of traumatic injuries to peripheral nerves.
周围神经损伤的处理对整形外科医生来说仍然是一个巨大的挑战。由于无法使轴突末端融合,显微外科神经修复后的效果一直不稳定。我们目前的神经修复策略依赖于轴突再生这一缓慢而漫长的过程(约1毫米/天)。聚乙二醇(PEG)已被作为一种潜在的轴突融合剂进行研究;然而,轴突融合的百分比并不稳定。本研究的目的是确定一种PEG递送装置,以规范在尝试用PEG进行轴突融合后的结果。
我们使用大鼠坐骨神经损伤模型,完全横断并修复左侧坐骨神经,在12周的时间跨度内评估PEG融合的疗效。此外,我们评估了一种递送装置在PEG融合后优化结果的能力。
我们发现,通过电生理学、荧光逆行示踪剂和扩散张量成像评估,PEG能迅速(在数分钟内)恢复轴突的连续性。免疫组织化学分析表明,在接受PEG治疗的动物中,术后1周、4周和12周时运动轴突计数显著增加。此外,与接受标准神经外膜修复的动物(对照动物)相比,PEG使行为功能恢复了高达50%。
PEG在神经切断术后迅速恢复神经功能的能力可能对外周神经创伤损伤的临床处理产生重大影响。