中国神经再生研究(英文版) ›› 2023, Vol. 18 ›› Issue (4): 814-818.doi: 10.4103/1673-5374.353498

• 原著:周围神经损伤修复保护与再生 • 上一篇    下一篇

再生坐骨周围神经横断后接口可防止神经瘤形成

  

  • 出版日期:2023-04-15 发布日期:2022-10-29
  • 基金资助:
    湖北省卫健委医学领军人才项目(LJ20200405)

Regenerative peripheral nerve interface prevents neuroma formation after peripheral nerve transection

Zheng Wang#, Xin-Zeyu Yi#, Ai-Xi Yu*   

  1. Department of Orthopedics Trauma and Microsurgery, Zhongnan Hospital of Wuhan University, Wuhan, Hubei Province, China
  • Online:2023-04-15 Published:2022-10-29
  • Contact: Ai-Xi Yu, MD, yuaixi@whu.edu.cn.
  • Supported by:
    This study was supported by the Health Commission of Hubei Province Medical Leading Talent Project, No. LJ20200405 (to AXY).

摘要:

周围神经横断后形成神经瘤通常导致严重的神经性疼痛。在临床中,再生周围神经接口被发现能够减少截肢后痛性神经瘤的发生,但是尚无相关机制的研究,且无再生周围神经接口与其他神经瘤预防手段的对比研究。因此,我们建立了左侧坐骨神经横断大鼠模型,以再生周围神经接口和神经残端肌肉植入分别进行干预,结果显示,与神经残端肌肉植入相比,行再生周围神经接口修复的大鼠坐骨神经近端中胶原纤维和不规则再生轴突的增殖受到抑制,纤维化标志物α-平滑肌肌动蛋白和炎症标志物Sigma-1受体的表达减少,自噬行为减少,损伤侧背根神经节中疼痛相关标志物c-fos和P物质减少,胶质细胞源性神经营养因子的表达增加。提示再生周围神经接口可抑制周围神经损伤引起的神经瘤形成和神经炎症,其机制可能与上调背根神经节中胶质细胞源性神经营养因子的表达有关。

https://orcid.org/0000-0002-5723-6140 (Ai-Xi Yu)

关键词: 创伤性神经瘤, 自伤, 神经性疼痛, 再生周围神经接口, 胶质细胞源性神经营养因子, 背根神经节, 周围神经, 神经损伤, 神经再生, 轴突逆行转运

Abstract: Neuroma formation after peripheral nerve transection often leads to severe neuropathic pain. Regenerative peripheral nerve interface has been shown to reduce painful neuroma in the clinic. However, no reports have investigated the underlying mechanisms, and no comparative animal studies on regenerative peripheral nerve interface and other means of neuroma prevention have been conducted to date. In this study, we established a rat model of left sciatic nerve transfection, and subsequently interfered with the model using the regenerative peripheral nerve interface or proximal nerve stump implantation inside a fully innervated muscle. Results showed that, compared with rats subjected to nerve stump implantation inside the muscle, rats subjected to regenerative peripheral nerve interface intervention showed greater inhibition of the proliferation of collagenous fibers and irregular regenerated axons, lower expressions of the fibrosis marker α-smooth muscle actin and the inflammatory marker sigma-1 receptor in the proximal nerve stump, lower autophagy behaviors, lower expressions of c-fos and substance P, higher expression of glial cell line-derived neurotrophic factor in the ipsilateral dorsal root ganglia. These findings suggested that regenerative peripheral nerve interface inhibits peripheral nerve injury-induced neuroma formation and neuropathic pain possibly via the upregulation of the expression of glial cell line-derived neurotrophic factor in the dorsal root ganglia and reducing neuroinflammation in the nerve stump.  

Key words: autotomy, dorsal root ganglia, glial cell line-derived neurotrophic factor, nerve injury, neuropathic pain, peripheral nerve, regeneration, regenerative peripheral nerve interface, retrograde axonal transport, traumatic neuroma