Second Department of Physiology, Kawasaki Medical School, 577, Matsushima, Kurashiki City, Okayama 701-0192, Japan.
Second Department of Physiology, Kawasaki Medical School, 577, Matsushima, Kurashiki City, Okayama 701-0192, Japan.
Exp Neurol. 2018 Jul;305:108-120. doi: 10.1016/j.expneurol.2018.04.006. Epub 2018 Apr 11.
Descending spinal pathways (corticospinal, rubrospinal, and reticulospinal) are believed to contribute to functional recovery resulting from rehabilitative training after stroke. However, the contribution of each pathway remains unclear. In the current study, we investigated rehabilitation-induced functional recovery and remodelling of the descending spinal pathways after severe cortical stroke in rats followed by 3 weeks of various rehabilitation [constraint-induced movement therapy (CIMT), skilled forelimb reaching, rotarod, and treadmill exercise]. Following photothrombotic stroke, 96% of corticospinal neurons in the ipsilesional motor cortex were destroyed. Despite the preservation of 82% of total spinal projection neurons (e.g. rubrospinal and reticulospinal projection neurons), rats showed persistent and severe disability, especially in skilled motor function. In this severe stroke model, only CIMT promoted functional recovery, associated with increased corticospinal projections from the peri-infarct motor cortex. Rehabilitation-induced recovery was reversed when the restored corticospinal neurons were destroyed by a second stroke. These data indicate that training-induced functional recovery is dependent on ipsilesional corticospinal projections, which highlights the importance of using strategies to enhance survival, axonal remodelling, or regeneration of corticospinal neurons to effectively restore function in severely affected stroke patients.
下行脊髓通路(皮质脊髓、红核脊髓和网状脊髓)被认为有助于中风后康复训练所导致的功能恢复。然而,每种通路的贡献仍然不清楚。在目前的研究中,我们研究了严重皮质性中风后大鼠的下行脊髓通路的康复诱导的功能恢复和重塑,随后进行了 3 周的各种康复治疗[强制性运动疗法(CIMT)、熟练前肢伸展、转棒和跑步机运动]。光血栓性中风后,同侧运动皮质中的 96%皮质脊髓神经元被破坏。尽管保留了 82%的总脊髓投射神经元(例如红核脊髓和网状脊髓投射神经元),大鼠仍表现出持续性和严重的残疾,特别是在熟练运动功能方面。在这种严重的中风模型中,只有 CIMT 促进了功能恢复,与梗死周围运动皮质的皮质脊髓投射增加有关。当恢复的皮质脊髓神经元被第二次中风破坏时,康复诱导的恢复就会逆转。这些数据表明,训练诱导的功能恢复依赖于同侧皮质脊髓投射,这突出了使用策略来增强皮质脊髓神经元的存活、轴突重塑或再生以有效恢复严重中风患者功能的重要性。