Centre for Neuroscience, University of Alberta, Edmonton, AB, Canada.
Behav Brain Res. 2013 Feb 15;239:31-42. doi: 10.1016/j.bbr.2012.10.047. Epub 2012 Nov 3.
Promoting the rewiring of lesioned motor tracts following a spinal cord injury is a promising strategy to restore motor function. For instance, axonal collaterals may connect to spared, lesion-bridging neurons, thereby establishing a detour for descending signals and thus promoting functional recovery. In our rat model of cervical spinal cord injury, we attempted to promote targeted rewiring of the unilaterally injured corticospinal tract (CST) via the spared reticulospinal tract (RtST). To promote new connections between the two tracts in the brainstem, we administered viral vectors producing two neurotrophins. Brain-derived neurotrophic factor (BDNF), a known promotor of collateral growth, was expressed in the motor cortex, and neurotrophin 3 (NT-3), which has chemoattractive properties, was expressed in the reticular formation. Because rehabilitative training has proven to be beneficial in promoting functionally meaningful plasticity following injury, we added training in a skilled reaching task. Different neurotrophin or control treatments with or without training were evaluated. As hypothesized, improvements of motor performance with the injured forelimb following neurotrophin treatment alone were absent or modest compared to untreated controls. In contrast, we found a significant synergistic effect on performance when BDNF treatment was combined with training. The mechanism of this recovery remains unidentified, as histological analyses of CST and RtST collateral projections did not reveal differences among treatment groups. In conclusion, we demonstrate that following a cervical spinal lesion, rehabilitative training is necessary to translate effects of BDNF into functional recovery by mechanisms which are likely independent of collateral sprouting of the CST or RtST into the gray matter.
促进脊髓损伤后受损运动束的再布线是恢复运动功能的一种很有前途的策略。例如,轴突侧支可能与保留的、桥接损伤的神经元相连,从而为下行信号建立一个旁路,从而促进功能恢复。在我们的颈段脊髓损伤大鼠模型中,我们试图通过保留的网状脊髓束(RtST)促进单侧损伤的皮质脊髓束(CST)的靶向再布线。为了促进脑干中两条束之间的新连接,我们给予了产生两种神经营养因子的病毒载体。脑源性神经营养因子(BDNF)是一种已知的侧支生长促进剂,在运动皮层中表达,神经营养因子 3(NT-3)具有趋化性,在网状结构中表达。由于康复训练已被证明在促进损伤后有意义的功能可塑性方面是有益的,所以我们增加了熟练的抓握任务训练。不同的神经营养因子或对照治疗(有或没有训练)进行了评估。正如假设的那样,与未治疗的对照组相比,单独使用神经营养因子治疗后受伤前肢的运动性能改善是不存在或适度的。相比之下,当 BDNF 治疗与训练相结合时,我们发现对性能有显著的协同作用。这种恢复的机制仍不清楚,因为 CST 和 RtST 侧支投射的组织学分析并没有显示出治疗组之间的差异。总之,我们证明了在颈段脊髓损伤后,康复训练对于将 BDNF 的作用转化为功能恢复是必要的,其机制可能与 CST 或 RtST 进入灰质的侧支发芽无关。