Unit of Oral and Maxillofacial Medicine and Surgery, School of Clinical Dentistry, University of Sheffield, Claremont Crescent, Sheffield S10 2TA, UK; Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Neuroscience. 2011 May 5;181:271-7. doi: 10.1016/j.neuroscience.2011.02.054. Epub 2011 Mar 4.
We have investigated the effect of three potential scar-reducing agents applied at a sciatic nerve repair site in C57-black-6 mice. Under anaesthesia the nerve was transected, repaired using four epineurial sutures, and 100 μl of either triamcinolone acetonide (1 mg/100 μl), an interleukin-10 peptide fragment (125 ng/100 μl or 500 ng/100 μl) or mannose-6-phosphate (M6P, 200 mM or 600 mM) was injected into and around the nerve. After 6 weeks the extent of regeneration was assessed electrophysiologically by determining the ratio of the compound action potential (CAP) modulus evoked by electrical stimulation of the nerve 2 mm distal or proximal to the repair site. The conduction velocity of the fastest components in the CAP was also calculated. The percentage area of collagen staining (PAS) at the repair site was analysed using Picrosirius Red and image analysis. Comparisons were made with a placebo group (100 μl of phosphate buffered saline) and sham-operated controls. The median CAP modulus ratio in the 600 mM M6P group was 0.44, which was significantly higher than in the placebo group (0.24, P=0.012: Kruskal-Wallis test). Conduction velocities were also faster in the 600 mM M6P group (median 30 m s(-1)) than in the placebo group (median 27.8 m s(-1); P=0.0197: Kruskal-Wallis test). None of the other treated groups were significantly different from the placebo, and all had significantly lower CAP ratios than the sham controls (P<0.05). All repair groups had a significantly higher PAS for collagen than sham controls. We conclude that the administration of 600 mM mannose-6-phosphate to a nerve repair site enhances axonal regeneration.
我们研究了三种潜在的疤痕减少剂在 C57-黑 6 小鼠坐骨神经修复部位的应用效果。在麻醉下,神经被横断,用四根神经外膜缝线修复,然后在神经内和周围注射 100 μl 曲安奈德(1 mg/100 μl)、白细胞介素-10 肽片段(125 ng/100 μl 或 500 ng/100 μl)或甘露糖-6-磷酸(M6P,200 mM 或 600 mM)。6 周后,通过测量电刺激神经 2mm 远端或近端时复合动作电位(CAP)模量的比值,从电生理学上评估再生程度。CAP 中最快成分的传导速度也被计算出来。使用苦味酸天狼猩红和图像分析,对修复部位的胶原染色(PAS)面积百分比进行分析。与安慰剂组(100 μl 磷酸盐缓冲盐水)和假手术对照组进行比较。600 mM M6P 组的 CAP 模量比中位数为 0.44,明显高于安慰剂组(0.24,P=0.012:Kruskal-Wallis 检验)。600 mM M6P 组的传导速度也较快(中位数 30 m s(-1)),明显快于安慰剂组(中位数 27.8 m s(-1);P=0.0197:Kruskal-Wallis 检验)。其他治疗组与安慰剂组均无显著差异,且 CAP 比值均明显低于假手术对照组(P<0.05)。所有修复组的胶原 PAS 均明显高于假手术对照组。我们得出结论,在神经修复部位给予 600 mM 甘露糖-6-磷酸可增强轴突再生。