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优化的眶内视神经暴露:大鼠模型中神经再生的转化外科范式

Optimized intraorbital optic nerve exposure: a translational surgical paradigm for neural regeneration in rat model.

作者信息

Zhu Hui, Li Guopei, Zhu Min, Ma Jinlei, Shen Peiyang, Zhang Si

机构信息

Department of Ophthalmology, The Second People's Hospital of Foshan, Foshan, 528000, Guangdong, China.

Department of Ophthalmology, The First People's Hospital of Foshan, Foshan, 528000, Guangdong, China.

出版信息

Int Ophthalmol. 2025 Jun 12;45(1):242. doi: 10.1007/s10792-025-03621-3.

Abstract

PURPOSE

To establish a standardized microsurgical protocol for atraumatic exposure of extended intraorbital optic nerve segments in rat models, enabling precision interventions in neural regeneration research.

METHODS

Aseptic surgical procedures were performed on anesthetized Sprague-Dawley rats, involving three critical steps: (1) precision skin incision with bilateral silk suture retraction, (2) meticulous periorbital adipose tissue dissection, and (3) atraumatic full-length optic nerve exposure. Post-exposure interventions comprised optic nerve crush (ONC) modeling, intrasheath injection, scaffold and hydrogel implantation. Validation encompassed functional (Functional Visual Evoked Potentials, FVEP), vascular (Fluorescein Fundus Angiography, FFA), and cellular (RGC density and axonal integrity via cholera toxin B subunit (CTB) anterograde tracing) assesments.

RESULTS

The approach reliably exposed 5-mm intraorbital optic nerve segments (4.96 ± 0.13 mm) with intact vasculature (FFA-confirmed perfusion). Complete ONC validation was demonstrated through three principal findings: (a) Complete FVEP signal ablation (Ampliude P1 (OS/OD) pre-operation 1.05 ± 0.19, sham 1.00 ± 0.06, ONC 0.03 ± 0.02, *  p < 0.05), (b) Progressive RGC loss quantified by CTB anterograde signal attenuation (Week 1: 1496.7 ± 186.3; Week 2: 146.3 ± 13.0; Week 3: 110.0 ± 12.4;Week 4: 78.75 ± 5.1, * p <  0.05), and (c) Axonal discontinuity confirmed by anterograde CTB truncation. Scaffold implantation permitted CTB-traced axonal regrowth across the lesion site.

CONCLUSION

This refined surgical protocol provides enhanced operative accessibility for optic nerve interventions, enabling precise modeling of neural injury and repair mechanisms while maintaining microvascular homeostasis. The technical reproducibility and quantifiable outcome measures establish a robust platform for translational research in neuroprotection and regenerative therapies.

摘要

目的

在大鼠模型中建立一种标准化的显微手术方案,用于无创伤暴露眶内视神经延长段,以便在神经再生研究中进行精确干预。

方法

对麻醉后的Sprague-Dawley大鼠进行无菌手术操作,包括三个关键步骤:(1)用双侧丝线缝合牵拉进行精确的皮肤切口,(2)细致地解剖眶周脂肪组织,(3)无创伤地暴露全长视神经。暴露后的干预措施包括视神经挤压(ONC)建模、鞘内注射、支架和水凝胶植入。验证包括功能(功能性视觉诱发电位,FVEP)、血管(荧光素眼底血管造影,FFA)和细胞(通过霍乱毒素B亚基(CTB)顺行追踪评估RGC密度和轴突完整性)评估。

结果

该方法可靠地暴露了5毫米的眶内视神经段(4.96±0.13毫米),血管系统完整(FFA证实有灌注)。通过三个主要发现证实了完全ONC验证:(a)FVEP信号完全消失(术前P1波幅(OS/OD)1.05±0.19,假手术组1.00±0.06,ONC组0.03±0.02,*p<0.05),(b)通过CTB顺行信号衰减量化的RGC逐渐丢失(第1周:1496.7±186.3;第2周:146.3±13.0;第3周:110.0±12.4;第4周:78.75±5.1,*p<0.05),以及(c)顺行CTB截断证实轴突连续性中断。支架植入允许CTB追踪的轴突在损伤部位再生。

结论

这种优化的手术方案为视神经干预提供了更好的手术可及性,能够在保持微血管稳态的同时,精确模拟神经损伤和修复机制。技术的可重复性和可量化的结果指标为神经保护和再生治疗的转化研究建立了一个强大的平台。

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