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Activity-Based Therapies for Repair of the Corticospinal System Injured during Development

机译:以活动为基础的治疗发展过程中受损的皮质脊髓系统的疗法

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摘要

This review presents the mechanistic underpinnings of corticospinal tract (CST) development, derived from animal models, and applies what has been learned to inform neural activity-based strategies for CST repair. We first discuss that, in normal development, early bilateral CST projections are later refined into a dense crossed CST projection, with maintenance of sparse ipsilateral projections. Using a novel mouse genetic model, we show that promoting the ipsilateral CST projection produces mirror movements, common in hemiplegic cerebral palsy (CP), suggesting that ipsilateral CST projections become maladaptive when they become abnormally dense and strong. We next discuss how animal studies support a developmental “competition rule” whereby more active/used connections are more competitive and overtake less active/used connections. Based on this rule, after unilateral injury the damaged CST is less able to compete for spinal synaptic connections than the uninjured CST. This can lead to a progressive loss of the injured hemisphere’s contralateral projection and a reactive gain of the undamaged hemisphere’s ipsilateral CST. Knowledge of the pathophysiology of the developing CST after injury informs interventional strategies. In an animal model of hemiplegic CP, promoting injured system activity or decreasing the uninjured system’s activity immediately after the period of a developmental injury both increase the synaptic competitiveness of the damaged system, contributing to significant CST repair and motor recovery. However, delayed intervention, despite significant CST repair, fails to restore skilled movements, stressing the need to consider repair strategies for other neural systems, including the rubrospinal and spinal interneuronal systems. Our interventional approaches harness neural activity-dependent processes and are highly effective in restoring function. These approaches are minimally invasive and are poised for translation to the human.
机译:这篇综述介绍了源自动物模型的皮质脊髓束(CST)发育的机械基础,并将所学知识应用于基于神经活动的CST修复策略。我们首先讨论,在正常发展中,早期的双边CST投影后来被细化为密集的交叉CST投影,并保持了同侧的稀疏投影。使用新型的小鼠遗传模型,我们显示促进同侧CST投射会产生偏瘫脑性瘫痪(CP)中常见的镜像运动,这表明当同侧CST投射变得异常密集和结实时会变得适应不良。接下来,我们将讨论动物研究如何支持发展的“竞争规则”,在这种规则中,较活跃/较常用的连接更具竞争性,而对较不活跃/较常用的连接的超越。基于此规则,单侧受伤后,受损的CST与未受伤的CST相比,竞争脊柱突触连接的能力较低。这可能导致受伤的半球的对侧投射逐渐丢失,而未受损的半球的同侧CST反应性增加。受伤后发展中的CST的病理生理知识可为介入策略提供参考。在偏瘫性CP的动物模型中,在发育损伤后立即促进受损系统的活动或降低未受损系统的活动都可以增加受损系统的突触竞争力,从而有助于显着的CST修复和运动恢复。然而,尽管进行了严重的CST修复,但延迟的干预仍无法恢复熟练的动作,从而强调了需要考虑其他神经系统(包括红松神经和脊髓神经内系统)的修复策略。我们的干预方法利用神经活动相关过程,在恢复功能方面非常有效。这些方法具有最小的侵入性,并准备将其翻译为人类。

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