Eggers Ruben, Tannemaat Martijn R, De Winter Fred, Malessy Martijn J A, Verhaagen Joost
Laboratory for Neuroregeneration, Netherlands Institute for Neuroscience, Meibergdreef 47, 1105 BA, Amsterdam, the Netherlands.
Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands.
Eur J Neurosci. 2016 Feb;43(3):318-35. doi: 10.1111/ejn.13089. Epub 2015 Oct 29.
Root avulsions due to traction to the brachial plexus causes complete and permanent loss of function. Until fairly recent, such lesions were considered impossible to repair. Here we review clinical repair strategies and current progress in experimental ventral root avulsion lesions. The current gold standard in patients with a root avulsion is nerve transfer, whereas reimplantation of the avulsed root into the spinal cord has been performed in a limited number of cases. These neurosurgical repair strategies have significant benefit for the patient but functional recovery remains incomplete. Developing new ways to improve the functional outcome of neurosurgical repair is therefore essential. In the laboratory, the molecular and cellular changes following ventral root avulsion and the efficacy of intervention strategies have been studied at the level of spinal motoneurons, the ventral spinal root and peripheral nerve, and the skeletal muscle. We present an overview of cell-based pharmacological and neurotrophic factor treatment approaches that have been applied in combination with surgical reimplantation. These interventions all demonstrate neuroprotective effects on avulsed motoneurons, often accompanied with various degrees of axonal regeneration. However, effects on survival are usually transient and robust axon regeneration over long distances has as yet not been achieved. Key future areas of research include finding ways to further extend the post-lesion survival period of motoneurons, the identification of neuron-intrinsic factors which can promote persistent and long-distance axon regeneration, and finally prolonging the pro-regenerative state of Schwann cells in the distal nerve.
臂丛神经受牵拉导致的神经根撕脱会造成功能完全且永久性丧失。直到最近,此类损伤还被认为无法修复。在此,我们回顾临床修复策略以及实验性腹侧神经根撕脱损伤的当前进展。目前,神经根撕脱患者的金标准治疗方法是神经移植,而将撕脱的神经根重新植入脊髓仅在少数病例中实施过。这些神经外科修复策略对患者有显著益处,但功能恢复仍不完全。因此,开发新方法以改善神经外科修复的功能结局至关重要。在实验室中,已在脊髓运动神经元、腹侧脊髓神经根和周围神经以及骨骼肌层面研究了腹侧神经根撕脱后的分子和细胞变化以及干预策略的效果。我们概述了基于细胞的药理学和神经营养因子治疗方法,这些方法已与手术再植入联合应用。这些干预措施均对撕脱的运动神经元显示出神经保护作用,通常伴有不同程度的轴突再生。然而,对存活的影响通常是短暂的,尚未实现长距离的强大轴突再生。未来关键的研究领域包括找到进一步延长损伤后运动神经元存活期的方法、识别可促进持续性和长距离轴突再生的神经元内在因子,以及最终延长远端神经中雪旺细胞的促再生状态。