Department of Neurophysiology and Brain Science, Nagoya City University Graduate School of Medicine, Nagoya 467-8601, Japan.
Section of Viral Vector Development, National Institute for Physiological Sciences, Okazaki 444-8585, Japan.
J Neurosci. 2019 Sep 11;39(37):7306-7320. doi: 10.1523/JNEUROSCI.0649-19.2019. Epub 2019 Aug 8.
Reorganization of residual descending motor circuits underlies poststroke recovery. We previously clarified a causal relationship between the cortico-rubral tract and intensive limb use-induced functional recovery after internal capsule hemorrhage (ICH). However, other descending tracts, such as the cortico-reticular tract, might also be involved in rehabilitation-induced compensation. To investigate whether rehabilitation-induced recovery after ICH involves a shift in the compensatory circuit from the cortico-rubral tract to the cortico-reticular tract, we established loss of function of the cortico-rubral tract or/and cortico-reticular tract using two sets of viral vectors comprising the Tet-on system and designer receptors exclusively activated by the designer drug system. We used an ICH model that destroyed almost 60% of the corticofugal fibers. Anterograde tracing in rehabilitated rats revealed abundant sprouting of axons from the motor cortex in the red nucleus but not in the medullary reticular formation during the early phase of recovery. This primary contribution of the cortico-rubral tract was demonstrated by its selective blockade, whereas selective cortico-reticular tract silencing had little effect. Interestingly, cortico-rubral tract blockade from the start of rehabilitation induced an obvious increase of axon sprouting in the reticular formation with substantial functional recovery. Additional cortico-reticular tract silencing under the cortico-rubral tract blockade significantly worsened the recovered forelimb function. Furthermore, the alternative recruitment of the cortico-reticular tract was gradually induced by intensive limb use under cortico-rubral tract blockade, in which cortico-reticular tract silencing caused an apparent motor deficit. These findings indicate that individual cortico-brainstem pathways have dynamic compensatory potency to support rehabilitative functional recovery after ICH. This study aimed to clarify the interaction between the cortico-rubral and the cortico-reticular tract during intensive rehabilitation and functional recovery after capsular stroke. Pathway-selective disturbance by two sets of viral vectors revealed that the cortico-rubral tract was involved in rehabilitation-induced recovery of forelimb function from an early phase after internal capsule hemorrhage, but that the cortico-reticular tract was not. The sequential disturbance of both tracts revealed that the cortico-reticular tract was recruited and involved in rehabilitation-induced recovery when the cortico-rubral tract failed to function. Our data demonstrate a dynamic compensatory action of individual cortico-brainstem pathways for recovery through poststroke rehabilitation.
梗死后运动通路的重组是恢复的基础。我们之前阐明了皮质-红核束与内囊出血(ICH)后强化肢体使用诱导的功能恢复之间的因果关系。然而,其他下行束,如皮质网状束,也可能参与康复诱导的代偿。为了研究 ICH 后康复诱导的恢复是否涉及从皮质-红核束到皮质网状束的补偿回路的转变,我们使用了两套包含 Tet-on 系统和仅由设计药物系统激活的设计受体的病毒载体来建立皮质-红核束或/和皮质网状束的功能丧失。我们使用了一种破坏皮质传出纤维近 60%的 ICH 模型。在康复大鼠的顺行追踪中,在恢复的早期阶段,大量来自运动皮层的轴突在红核中发芽,但不在延髓网状结构中发芽。通过选择性阻断证实了皮质-红核束的这种主要贡献,而选择性皮质网状束沉默则没有效果。有趣的是,从康复开始阻断皮质-红核束会导致网状结构中的轴突发芽明显增加,并伴有显著的功能恢复。在皮质-红核束阻断下进一步沉默皮质网状束会显著恶化恢复的前肢功能。此外,在皮质-红核束阻断下,密集的肢体使用会逐渐诱导皮质网状束的替代募集,其中皮质网状束沉默会导致明显的运动缺陷。这些发现表明,个体皮质-脑干通路具有动态代偿能力,可支持 ICH 后康复性功能恢复。本研究旨在阐明皮质-红核束和皮质网状束在 capsular 卒中后的强化康复和功能恢复期间的相互作用。通过两套病毒载体进行的通路选择性干扰表明,皮质-红核束参与了内囊出血后早期的前肢功能康复诱导恢复,但皮质网状束不参与。两条通路的顺序干扰表明,当皮质-红核束无法发挥作用时,皮质网状束被募集并参与康复诱导的恢复。我们的数据证明了个体皮质-脑干通路通过卒中后康复具有动态代偿作用。