Department of Neurosciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
Department of Quantitative Health Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
Neurorehabil Neural Repair. 2024 Dec;38(11-12):808-819. doi: 10.1177/15459683241277194. Epub 2024 Aug 31.
We previously demonstrated that deep brain stimulation (DBS) of lateral cerebellar nucleus (LCN) can enhance motor recovery and functional reorganization of perilesional cortex in rodent models of stroke or TBI.
Considering the treatment-related neuroplasticity observed at the perilesional cortex, we hypothesize that chronic LCN DBS-enhanced motor recovery observed will carry-over even after DBS has been deactivated.
Here, we directly tested the enduring effects of LCN DBS in male Long Evans rats that underwent controlled cortical impact (CCI) injury targeting sensorimotor cortex opposite their dominant forepaw followed by unilateral implantation of a macroelectrode into the LCN opposite the lesion. Animals were randomized to DBS or sham treatment for 4 weeks during which the motor performance were characterize by behavioral metrics. After 4 weeks, stimulation was turned off, with assessments continuing for an additional 2 weeks. Afterward, all animals were euthanized, and tissue was harvested for further analyses.
Treated animals showed significantly greater motor improvement across all behavioral metrics relative to untreated animals during the 4-week treatment, with functional gains persisting across 2-week post-treatment. This motor recovery was associated with the increase in CaMKIIα and BDNF positive cell density across perilesional cortex in treated animals.
LCN DBS enhanced post-TBI motor recovery, the effect of which was persisted up to 2 weeks beyond stimulation offset. Such evidence should be considered in relation to future translational efforts as, unlike typical DBS applications, treatment may only need to be provided until such time as a new function plateau is achieved.
我们之前的研究表明,小脑外侧核(LCN)的深部脑刺激(DBS)可以增强中风或 TBI 啮齿动物模型中病灶周围皮层的运动恢复和功能重组。
鉴于病灶周围皮层观察到的与治疗相关的神经可塑性,我们假设即使在 DBS 已停用后,慢性 LCN DBS 增强的运动恢复也将持续存在。
在这里,我们直接测试了 LCN DBS 在接受针对对侧优势前爪感觉运动皮层的控制性皮质撞击(CCI)损伤后,对侧 LCN 植入单极微电极的雄性长爪田鼠中的持久效应。动物随机分为 DBS 或假处理组,进行 4 周的治疗,在此期间通过行为指标来评估运动表现。4 周后,关闭刺激,继续评估 2 周。之后,所有动物被安乐死,采集组织进行进一步分析。
与未治疗动物相比,治疗动物在 4 周的治疗期间在所有行为指标上都表现出显著更大的运动改善,并且在治疗后 2 周仍保持功能改善。这种运动恢复与治疗动物病灶周围皮层中 CaMKIIα 和 BDNF 阳性细胞密度的增加有关。
LCN DBS 增强了 TBI 后的运动恢复,其效果在刺激停止后持续了 2 周。这种证据应该在未来的转化研究中考虑,因为与典型的 DBS 应用不同,治疗可能只需要提供到达到新的功能平台为止。