Carry-Over Effect of Deep Cerebellar Stimulation-Mediated Motor Recovery in a Rodent Model of Traumatic Brain Injury

刺激 运动皮层 神经可塑性 神经科学 脑深部刺激 初级运动皮层 创伤性脑损伤 脑刺激 医学 心理学 自然恢复 病变 物理医学与康复 冲程(发动机) 外科 内科学 帕金森病 疾病 精神科 机械工程 工程类
作者
Hugh H. Chan,Beth E. Fisher,Margaret A. Oimoen,Latavya Chintada,Hemant Khanna,Claire Sonneborn,Olivia Hogue,André G. Machado,Kenneth B. Baker
出处
期刊:Neurorehabilitation and Neural Repair [SAGE]
标识
DOI:10.1177/15459683241277194
摘要

Background 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. Objective 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. Methods 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. Results 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. Conclusions 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.
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