Hansen Christopher N, Faw Timothy D, White Susan, Buford John A, Grau James W, Basso D Michele
School of Health and Rehabilitation Sciences, The Ohio State UniversityColumbus, OH, USA; Center for Brain and Spinal Cord Repair, The Ohio State UniversityColumbus, OH, USA.
School of Health and Rehabilitation Sciences, The Ohio State UniversityColumbus, OH, USA; Center for Brain and Spinal Cord Repair, The Ohio State UniversityColumbus, OH, USA; Neuroscience Graduate Program, The Ohio State UniversityColumbus, OH, USA.
Front Neural Circuits. 2016 Mar 2;10:11. doi: 10.3389/fncir.2016.00011. eCollection 2016.
This study evaluated the role of spared axons on structural and behavioral neuroplasticity in the lumbar enlargement after a thoracic spinal cord injury (SCI). Previous work has demonstrated that recovery in the presence of spared axons after an incomplete lesion increases behavioral output after a subsequent complete spinal cord transection (TX). This suggests that spared axons direct adaptive changes in below-level neuronal networks of the lumbar cord. In response to spared fibers, we postulate that lumbar neuron networks support behavioral gains by preventing aberrant plasticity. As such, the present study measured histological and functional changes in the isolated lumbar cord after complete TX or incomplete contusion (SCI). To measure functional plasticity in the lumbar cord, we used an established instrumental learning paradigm (ILP). In this paradigm, neural circuits within isolated lumbar segments demonstrate learning by an increase in flexion duration that reduces exposure to a noxious leg shock. We employed this model using a proof-of-principle design to evaluate the role of sparing on lumbar learning and plasticity early (7 days) or late (42 days) after midthoracic SCI in a rodent model. Early after SCI or TX at 7 days, spinal learning was unattainable regardless of whether the animal recovered with or without axonal substrate. Failed learning occurred alongside measures of cell soma atrophy and aberrant dendritic spine expression within interneuron populations responsible for sensorimotor integration and learning. Alternatively, exposure of the lumbar cord to a small amount of spared axons for 6 weeks produced near-normal learning late after SCI. This coincided with greater cell soma volume and fewer aberrant dendritic spines on interneurons. Thus, an opportunity to influence activity-based learning in locomotor networks depends on spared axons limiting maladaptive plasticity. Together, this work identifies a time dependent interaction between spared axonal systems and adaptive plasticity in locomotor networks and highlights a critical window for activity-based rehabilitation.
本研究评估了保留轴突在胸段脊髓损伤(SCI)后腰膨大处结构和行为神经可塑性中的作用。先前的研究表明,不完全损伤后保留轴突的情况下恢复,会增加随后完全脊髓横断(TX)后的行为输出。这表明保留轴突可引导腰段脊髓以下水平神经元网络的适应性变化。针对保留的纤维,我们推测腰段神经元网络通过防止异常可塑性来支持行为改善。因此,本研究测量了完全TX或不完全挫伤(SCI)后分离的腰段脊髓的组织学和功能变化。为了测量腰段脊髓的功能可塑性,我们使用了一种既定的工具性学习范式(ILP)。在这个范式中,分离的腰段节段内的神经回路通过增加屈曲持续时间来减少暴露于有害腿部电击,从而表现出学习能力。我们采用这个模型,通过原理验证设计来评估在啮齿动物模型中胸段SCI早期(7天)或晚期(42天)保留对腰段学习和可塑性的作用。在SCI或TX后7天的早期,无论动物是否有轴突底物恢复,脊髓学习都无法实现。学习失败与负责感觉运动整合和学习的中间神经元群体中的细胞体萎缩和异常树突棘表达的测量结果同时出现。相反,在SCI后晚期,将腰段脊髓暴露于少量保留轴突6周可产生接近正常的学习。这与中间神经元上更大的细胞体体积和更少的异常树突棘相吻合。因此,影响运动网络中基于活动的学习的机会取决于保留轴突限制适应不良的可塑性。总之,这项工作确定了保留轴突系统与运动网络中适应性可塑性之间的时间依赖性相互作用,并突出了基于活动的康复的关键窗口。