Department of Orthopedics and Trauma, Key Laboratory of Trauma and Neural Regeneration (Ministry of Education/Peking University, Peking University People's Hospital, Beijing, 100044, China.
CNS Neurosci Ther. 2021 Jul;27(7):805-819. doi: 10.1111/cns.13640. Epub 2021 Apr 10.
Peripheral nerve defects are often difficult to recover from, and there is no optimal repair method. Therefore, it is important to explore new methods of repairing peripheral nerve defects. This study explored the efficacy of nerve grafts constructed from chitin biological conduits combined with small autogenous nerves (SANs) and platelet-rich plasma (PRP) for repairing 10-mm sciatic nerve defects in rats.
To prepare 10-mm sciatic nerve defects, SANs were first harvested and PRP was extracted. The nerve grafts consisted of chitin biological conduits combined with SAN and PRP, and were used to repair rat sciatic nerve defects. These examinations, including measurements of axon growth efficiency, a gait analysis, electrophysiological tests, counts of regenerated myelinated fibers and observations of their morphology, histological evaluation of the gastrocnemius muscle, retrograde tracing with Fluor-Gold (FG), and motor endplates (MEPs) distribution analysis, were conducted to evaluate the repair status.
Two weeks after nerve transplantation, the rate and number of regenerated axons in the PRP-SAN group improved compared with those in the PRP, SAN, and Hollow groups. The PRP-SAN group exhibited better recovery in terms of the sciatic functional index value, composite action potential intensity, myelinated nerve fiber density, myelin sheath thickness, and gastrectomy tissue at 12 weeks after transplantation, compared with the PRP and SAN groups. The results of FG retrograde tracing and MEPs analyses showed that numbers of FG-positive sensory neurons and motor neurons as well as MEPs distribution density were higher in the PRP-SAN group than in the PRP or SAN group.
Nerve grafts comprising chitin biological conduits combined with SANs and PRP significantly improved the repair of 10-mm sciatic nerve defects in rats and may have therapeutic potential for repairing peripheral nerve defects in future applications.
周围神经缺损往往难以恢复,目前尚无理想的修复方法。因此,探索修复周围神经缺损的新方法非常重要。本研究探讨了壳聚糖生物导管联合小自体神经(SAN)和富血小板血浆(PRP)构建的神经移植物修复大鼠 10mm 坐骨神经缺损的疗效。
制备 10mm 坐骨神经缺损,首先采集 SAN 并提取 PRP。神经移植物由壳聚糖生物导管与 SAN 和 PRP 结合而成,用于修复大鼠坐骨神经缺损。通过轴突生长效率测量、步态分析、电生理测试、再生有髓神经纤维计数及其形态观察、腓肠肌组织学评价、荧光金(FG)逆行追踪和运动终板(MEPs)分布分析等检查评估修复状态。
神经移植后 2 周,PRP-SAN 组的再生轴突率和数量较 PRP、SAN 和空心组均有改善。PRP-SAN 组在坐骨神经功能指数值、复合动作电位强度、有髓神经纤维密度、髓鞘厚度和移植后 12 周腓肠肌组织方面的恢复情况均优于 PRP 和 SAN 组。FG 逆行追踪和 MEPs 分析结果显示,PRP-SAN 组 FG 阳性感觉神经元和运动神经元的数量以及 MEPs 分布密度均高于 PRP 或 SAN 组。
壳聚糖生物导管联合 SAN 和 PRP 的神经移植物显著改善了大鼠 10mm 坐骨神经缺损的修复效果,可能为未来应用修复周围神经缺损提供治疗潜力。