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

Neurorehabilitation and neural repair Pub Date : 2024-12-01 Epub Date: 2024-08-31 DOI:10.1177/15459683241277194
Hugh H Chan, Brittany M Fisher, Margaret A Oimoen, Latavya Chintada, Hemen Khanna, Claire A Sonneborn, Olivia Hogue, André G Machado, Kenneth B Baker
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Abstract

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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创伤性脑损伤啮齿动物模型中小脑深部刺激介导的运动恢复的延续性效应
背景:我们以前曾证实,在中风或创伤性脑损伤的啮齿类动物模型中,对小脑外侧核(LCN)进行深部脑刺激(DBS)可促进运动恢复和外周皮层的功能重组:方法:在这里,我们直接测试了 LCN DBS 对雄性 Long Evans 大鼠的持久影响,这些大鼠接受了针对其优势前爪对面感觉运动皮层的控制性皮层冲击(CCI)损伤,然后在病变对面的 LCN 单侧植入了大电极。动物被随机分配到 DBS 或假治疗中,为期 4 周,在此期间,动物的运动表现将通过行为指标来描述。4 周后,关闭刺激,继续评估 2 周。之后,对所有动物实施安乐死,并采集组织进行进一步分析:结果:与未接受治疗的动物相比,接受治疗的动物在为期4周的治疗期间在所有行为指标上的运动能力都有明显改善,并且在治疗后2周内仍能保持功能改善。这种运动功能的恢复与治疗动物髂周皮层中 CaMKIIα 和 BDNF 阳性细胞密度的增加有关:结论:LCN DBS 可促进创伤后运动恢复,其效果可在刺激消失后持续 2 周。这些证据应在未来的转化工作中加以考虑,因为与典型的 DBS 应用不同,治疗可能只需要持续到实现新的功能稳定为止。
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