Center for Neurological Restoration, Neurological Institute and Departments of Neuroscience and.
Center for Neurological Restoration, Neurological Institute and Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, and.
J Neurosci. 2014 Jul 2;34(27):9040-50. doi: 10.1523/JNEUROSCI.0953-14.2014.
Control over postinjury CNS plasticity is a major frontier of science that, if conquered, would open new avenues for treatment of neurological disorders. Here we investigate the functional, physiological, and structural changes in the cerebral cortex associated with chronic deep brain stimulation of the cerebellar output, a treatment approach that has been shown to improve postischemia motor recovery in a rodent model of cortical infarcts. Long-Evans rats were pretrained on the pasta-matrix retrieval task, followed by induction of focal cortical ischemia and implantation of a macroelectrode in the contralesional lateral cerebellar nucleus. Animals were assigned to one of three treatment groups pseudorandomly to balance severity of poststroke motor deficits: REGULAR stimulation, BURST stimulation, or SHAM. Treatment initiated 2 weeks post surgery and continued for 5 weeks. At the end, animals were randomly selected for perilesional intracortical microstimulation mapping and tissue sampling for Western blot analysis or contributed tissue for 3D electron microscopy. Evidence of enhanced cortical plasticity with therapeutically effective stimulation is shown, marked by greater perilesional reorganization in stimulation- treated animals versus SHAM. BURST stimulation was significantly effective for promoting distal forepaw cortical representation. Stimulation-treated animals showed a twofold increase in synaptic density compared with SHAM. In addition, treated animals demonstrated increased expression of synaptic markers of long-term potentiation and plasticity, including synaptophysin, NMDAR1, CaMKII, and PSD95. These findings provide a critical foundation of how deep cerebellar stimulation may guide plastic reparative reorganization after nonprogressive brain injury and indicate strong translational potential.
控制损伤后中枢神经系统可塑性是科学的一个主要前沿领域,如果攻克这一领域,将为治疗神经紊乱开辟新的途径。在这里,我们研究了与小脑输出的慢性深部脑刺激相关的大脑皮层的功能、生理和结构变化,这种治疗方法已被证明可以改善皮质梗死啮齿动物模型中的缺血后运动恢复。长耳大鼠先在面食基质检索任务中进行预训练,然后诱导皮质局灶性缺血,并在对侧外侧小脑核中植入一个宏观电极。动物随机分配到三个治疗组中的一个,以平衡中风后运动缺陷的严重程度:常规刺激、爆发刺激或假刺激。治疗从手术后两周开始,持续五周。最后,随机选择动物进行损伤周围皮质内微刺激映射和组织取样进行 Western blot 分析,或为 3D 电子显微镜提供组织。有证据表明,具有治疗效果的刺激增强了皮质可塑性,刺激治疗动物的损伤周围组织重组程度大于假刺激。爆发刺激对促进远侧前爪皮质代表区具有显著效果。与假刺激相比,刺激治疗动物的突触密度增加了两倍。此外,治疗动物还表现出突触长时程增强和可塑性的标志物表达增加,包括突触小体蛋白、NMDAR1、CaMKII 和 PSD95。这些发现为深部小脑刺激如何引导非进行性脑损伤后的可塑性修复性重组提供了重要基础,并表明具有很强的转化潜力。