Surgical and Orthopaedic Research Laboratories (SORL), Prince of Wales Clinical School, Faculty of Medicine, University of New South Wales (UNSW) Sydney, Prince of Wales Hospital, Sydney, NSW, Australia.
Eur Spine J. 2024 May;33(5):2097-2115. doi: 10.1007/s00586-024-08153-5. Epub 2024 Feb 19.
To evaluate the biological and biomechanical effects of fenestration/microdiscectomy in an in vivo rabbit model, and in doing so, create a preclinical animal model of IVDD.
Lateral lumbar IVD fenestration was performed in vivo as single- (L3/4; n = 12) and multi-level (L2/3, L3/4, L4/5; n = 12) fenestration in skeletally mature 6-month-old New Zealand White rabbits. Radiographic, micro-CT, micro-MRI, non-destructive robotic range of motion, and histological evaluations were performed 6- and 12-weeks postoperatively. Independent t tests, one-way and two-way ANOVA and Kruskal-Wallis tests were used for parametric and nonparametric data, respectively. Statistical significance was set at P < 0.05.
All rabbits recovered uneventfully from surgery and ambulated normally. Radiographs and micro-CT demonstrated marked reactive proliferative osseous changes and endplate sclerosis at fenestrated IVDs. Range of motion at the fenestrated disc space was significantly reduced compared to intact controls at 6- and 12-weeks postoperatively (P < 0.05). Mean disc height index percentage for fenestrated IVDs was significantly lower than adjacent, non-operated IVDs for both single and multi-level groups, at 6 and 12 weeks (P < 0.001). Pfirrmann MRI IVDD and histological grading scores were significantly higher for fenestrated IVDs compared to non-operated adjacent and age-matched control IVDs for single and multi-level groups at 6 and 12 weeks (P < 0.001).
Fenestration, akin to microdiscectomy, demonstrated significant biological, and biomechanical effects in this in vivo rabbit model and warrants consideration by veterinary and human spine surgeons. This described model may be suitable for preclinical in vivo evaluation of therapeutic strategies for IVDD in veterinary and human patients.
在活体兔模型中评估开窗/微椎间盘切除术的生物学和生物力学效应,并由此建立 IVDD 的临床前动物模型。
在骨骼成熟的 6 月龄新西兰白兔中进行单侧(L3/4;n=12)和多节段(L2/3、L3/4、L4/5;n=12)开窗术。术后 6 周和 12 周分别进行影像学、微 CT、微 MRI、非破坏性机器人运动范围和组织学评估。分别采用独立 t 检验、单因素和双因素 ANOVA 以及 Kruskal-Wallis 检验对参数和非参数数据进行分析。统计学意义设定为 P<0.05。
所有兔子均顺利从手术中恢复并正常行走。X 线片和微 CT 显示,开窗的椎间盘有明显的反应性增生性骨改变和终板硬化。与未手术的对照组相比,开窗节段的运动范围在术后 6 周和 12 周时显著减小(P<0.05)。与相邻未手术的椎间盘相比,单节段和多节段开窗椎间盘的椎间盘高度指数百分比在术后 6 周和 12 周时均显著降低(P<0.001)。单节段和多节段开窗椎间盘的 Pfirrmann MRI 椎间盘退变和组织学分级评分均显著高于未手术的相邻和年龄匹配的对照组椎间盘,在术后 6 周和 12 周时均显著升高(P<0.001)。
开窗术类似于微椎间盘切除术,在该活体兔模型中显示出显著的生物学和生物力学效应,值得兽医和人类脊柱外科医生考虑。这种描述的模型可能适合兽医和人类患者 IVDD 治疗策略的临床前体内评估。