Institute of Pathophysiology, Faculty of Medicine, University of Ljubljana, Slovenia.
J Neurotrauma. 2012 Dec 10;29(18):2805-15. doi: 10.1089/neu.2011.2298. Epub 2012 Nov 19.
The influence of breaching the connective sheaths of the donor sural nerve on axonal sprouting into the end-to-side coapted peroneal nerve was examined in the rat. In parallel, the effect of these procedures on the donor nerve was assessed. The sheaths of the donor nerve at the coaptation site were either left completely intact (group A) or they were breached by epineurial sutures (group B), an epineurial window (group C), or a perineurial window (group D). In group A, the compound action potential (CAP) of sensory axons was detected in ~10% and 40% of the recipient nerves at 4 and 8 weeks, respectively, which was significantly less frequently than in group D at both recovery periods. In addition, the number of myelinated axons in the recipient nerve was significantly larger in group D than in other groups at 4 weeks. At 8 weeks, the number of axons in group A was only ~15% of the axon numbers in other groups (p<0.05). Focal subepineurial degenerative changes in the donor nerves were only seen after 4 weeks, but not later. The average CAP area and the total number of myelinated axons in the donor nerves were not different among the experimental groups. In conclusion, myelinated sensory axons are able to penetrate the epiperineurium of donor nerves after end-to-side nerve coaption; however, their ingrowth into recipient nerves is significantly enhanced by breaching the epiperineurial sheets at the coaptation site. Breaching does not cause permanent injury to the donor nerve.
研究了在大鼠中破坏供体腓肠神经的连接鞘对轴突向侧侧吻合的腓神经发芽的影响。同时,评估了这些程序对供体神经的影响。在吻合部位,供体神经的鞘要么完全保留完整(A 组),要么通过神经外膜缝线(B 组)、神经外膜窗(C 组)或神经内膜窗(D 组)破坏。在 A 组中,在 4 周和 8 周时,分别有10%和 40%的受神经中检测到感觉轴突的复合动作电位(CAP),这明显低于两个恢复期间的 D 组。此外,在 4 周时,D 组受神经中的有髓轴突数量明显多于其他组。在 8 周时,A 组的轴突数量仅为其他组轴突数量的15%(p<0.05)。供体神经中的局灶性亚神经外膜退行性改变仅在 4 周后可见,但此后不可见。供体神经中的平均 CAP 面积和有髓轴突总数在实验组之间没有差异。总之,有髓感觉轴突能够穿透侧侧吻合供体神经的神经外膜;然而,在吻合部位破坏神经外膜片可以显著增强其进入受神经的生长。破坏不会对供体神经造成永久性损伤。