中国神经再生研究(英文版) ›› 2025, Vol. 20 ›› Issue (9): 2667-2681.doi: 10.4103/NRR.NRR-D-23-01846

• 原著:周围神经损伤修复保护与再生 • 上一篇    下一篇

聚乙二醇融合修复横断坐骨神经促进不同品系雌雄大鼠伤害感知觉的恢复

  

  • 出版日期:2025-09-15 发布日期:2024-12-30

Polyethylene glycol fusion repair of severed sciatic nerves accelerates recovery of nociceptive sensory perceptions in male and female rats of different strains

Liwen Zhou1 , Karthik Venkudusamy1 , Emily A. Hibbard2 , Yessenia Montoya1 , Alexa Olivarez1 , Cathy Z. Yang1 , Adelaide Leung3 , Varun Gokhale1 , Guhan Periyasamy1 , Zeal Pathak1 , Dale R. Sengelaub2 , George D. Bittner1, *   

  1. 1 Department of Neuroscience, University of Texas, Austin, TX, USA; 2 Program in Neuroscience, Indiana University, Bloomington, IN, USA;  3 Department of Molecular Biosciences, University of Texas, Austin, TX, USA
  • Online:2025-09-15 Published:2024-12-30
  • Contact: George D. Bittner, PhD, bittner@austin.utexas.edu.
  • Supported by:
    This study was supported by DOD AFIRM III W81XWH-20-2-0029 subcontract; UT POC19-1774-13; Neuraptive Therapeutics Inc. 26-7724-56 and NIH R01-NS128086 grants; Lone Star Paralysis gift (to GDB).

摘要:


据报道,聚乙二醇融合对周围神经损伤后对轴突的修复是成功的;但聚乙二醇融合修复后感觉行为的恢复尚需进一步探讨。实验旨在探讨聚乙二醇融合是否能促进雄性和雌性SD大鼠和Lewis大鼠坐骨神经横断后的机械痛觉恢复。应用von Frey 测痛实验评估坐骨神经横断后的机械痛觉敏感性。发现坐骨神经介导的外侧背侧区域的基线机械缩足阈值在不同动物品系之间存在显著差异,但在不同性别之间无显著差异。坐骨神经横断后,所有大鼠对损伤同侧后爪外侧背区的刺激都表现出严重的低敏感性。然而,与对照组大鼠相比,融合聚乙二醇的大鼠恢复到基线戒断阈值的时间明显更早。此外,修复后4周或4周后坐骨神经功能指数显著提高的聚乙二醇融合大鼠与神经功能指数未恢复的大鼠相比,机械痛觉恢复得更早,但与大鼠的性别或品系无关。此外,大鼠伤害感知觉加速恢复到基线完全是由于聚乙二醇融合坐骨神经,而不是隐神经侧支的生长。在长达12周的时间里,没有任何大鼠出现慢性过敏反应。以上数据表明,聚乙二醇融合修复横断的坐骨神经可能会带来重要的临床益处。


https://orcid.org/0000-0002-5610-6264 (George D. Bittner)


Abstract: Successful polyethylene glycol fusion (PEG-fusion) of severed axons following peripheral nerve injuries for PEG-fused axons has been reported to: (1) rapidly restore electrophysiological continuity; (2) prevent distal Wallerian Degeneration and maintain their myelin sheaths; (3) promote primarily motor, voluntary behavioral recoveries as assessed by the Sciatic Functional Index; and, (4) rapidly produce correct and incorrect connections in many possible combinations that produce rapid and extensive recovery of functional peripheral nervous system/central nervous system connections and reflex (e.g., toe twitch) or voluntary behaviors. The preceding companion paper describes sensory terminal field reorganization following PEG-fusion repair of sciatic nerve transections or ablations; however, sensory behavioral recovery has not been explicitly explored following PEG-fusion repair. In the current study, we confirmed the success of PEG-fusion surgeries according to criteria (1–3) above and more extensively investigated whether PEG-fusion enhanced mechanical nociceptive recovery following sciatic transection in male and female outbred Sprague–Dawley and inbred Lewis rats. Mechanical nociceptive responses were assessed by measuring withdrawal thresholds using von Frey filaments on the dorsal and midplantar regions of the hindpaws. Dorsal von Frey filament tests were a more reliable method than plantar von Frey filament tests to assess mechanical nociceptive sensitivity following sciatic nerve transections. Baseline withdrawal thresholds of the sciatic-mediated lateral dorsal region differed significantly across strain but not sex. Withdrawal thresholds did not change significantly from baseline in chronic Unoperated and Sham-operated rats. Following sciatic transection, all rats exhibited severe hyposensitivity to stimuli at the lateral dorsal region of the hindpaw ipsilateral to the injury. However, PEG-fused rats exhibited significantly earlier return to baseline withdrawal thresholds than Negative Control rats. Furthermore, PEG-fused rats with significantly improved Sciatic Functional Index scores at or after 4 weeks postoperatively exhibited yet-earlier von Frey filament recovery compared with those without Sciatic Functional Index recovery, suggesting a correlation between successful PEG-fusion and both motor-dominant and sensory-dominant behavioral recoveries. This correlation was independent of the sex or strain of the rat. Furthermore, our data showed that the acceleration of von Frey filament sensory recovery to baseline was solely due to the PEG-fused sciatic nerve and not saphenous nerve collateral outgrowths. No chronic hypersensitivity developed in any rat up to 12 weeks. All these data suggest that PEG-fusion repair of transection peripheral nerve injuries could have important clinical benefits.

Key words: autophagia,  axotomy,  collateral sprouting,  neuropathic pain,  peripheral nerve repair,  polyethylene glycol fusion (PEG-fusion),   saphenous nerve,  sensory neurons,  sex and strain,  Wallerian degeneration