Lu Paul, Tuszynski Mark H
Department of Neurosciences, University of California San Diego, La Jolla, CA 92093-0626, USA.
Exp Neurol. 2008 Feb;209(2):313-20. doi: 10.1016/j.expneurol.2007.08.004. Epub 2007 Aug 22.
There has been remarkable progress in the last 20 years in understanding mechanisms that underlie the success of axonal regeneration in the peripheral nervous system, and the failure of axonal regeneration in the central nervous system. Following the identification of these underlying mechanisms, several distinct therapeutic approaches have been tested in in vivo models of spinal cord injury (SCI) to enhance central axonal structural plasticity, including the therapeutic administration of neurotrophic factors. While several tested mechanisms apparently enhance axonal growth, more recent, properly controlled studies indicate that experimental approaches to combine therapies that target distinct neural mechanisms achieve greater axonal growth than therapies applied in isolation. The search for combination therapies that optimize axonal growth after SCI continues.
在过去20年里,我们对周围神经系统轴突再生成功以及中枢神经系统轴突再生失败背后机制的理解取得了显著进展。在确定这些潜在机制之后,人们在脊髓损伤(SCI)的体内模型中测试了几种不同的治疗方法,以增强中枢轴突结构可塑性,包括神经营养因子的治疗性给药。虽然一些经过测试的机制显然能促进轴突生长,但最近经过适当对照的研究表明,针对不同神经机制的联合治疗方法比单独应用的治疗方法能实现更大程度的轴突生长。对脊髓损伤后优化轴突生长的联合治疗方法的探索仍在继续。