Gordon Tessa, Udina Esther, Verge Valerie M K, de Chaves Elena I Posse
Division of Physical Medicine and Rehabilitation, University of Alberta, Edmonton, Alberta.
Motor Control. 2009 Oct;13(4):412-41. doi: 10.1123/mcj.13.4.412.
Injured peripheral but not central nerves regenerate their axons but functional recovery is often poor. We demonstrate that prolonged periods of axon separation from targets and Schwann cell denervation eliminate regenerative capacity in the peripheral nervous system (PNS). A substantial delay of 4 weeks for all regenerating axons to cross a site of repair of sectioned nerve contributes to the long period of separation. Findings that 1h 20Hz bipolar electrical stimulation accelerates axon outgrowth across the repair site and the downstream reinnervation of denervated muscles in rats and human patients, provides a new and exciting method to improve functional recovery after nerve injuries. Drugs that elevate neuronal cAMP and activate PKA promote axon outgrowth in vivo and in vitro, mimicking the electrical stimulation effect. Rapid expression of neurotrophic factors and their receptors and then of growth associated proteins thereafter via cAMP, is the likely mechanism by which electrical stimulation accelerates axon outgrowth from the site of injury in both peripheral and central nervous systems.
受损的外周神经而非中枢神经能够再生其轴突,但功能恢复往往不佳。我们证明,轴突与靶标长期分离以及雪旺细胞去神经支配会消除外周神经系统(PNS)的再生能力。所有再生轴突穿过切断神经的修复部位存在长达4周的显著延迟,这导致了长时间的分离。有研究发现,1小时20赫兹的双极电刺激可加速大鼠和人类患者轴突跨越修复部位生长以及去神经肌肉的下游再支配,这为改善神经损伤后的功能恢复提供了一种全新且令人兴奋的方法。提高神经元cAMP水平并激活PKA的药物在体内和体外均能促进轴突生长,模拟了电刺激的效果。神经营养因子及其受体随后通过cAMP快速表达,接着生长相关蛋白也快速表达,这可能是电刺激加速外周和中枢神经系统损伤部位轴突生长的机制。