Evidence map›Paper›PMID 39215643›Full record

ArticleNeurorehabilitation and neural repair2024

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

Hugh H Chan, Brittany M Fisher, Margaret A Oimoen, Latavya Chintada, Hemen Khanna, Claire A Sonneborn, Olivia Hogue, André G Machado, Kenneth B Baker

Abstract read
In one paragraph

Article in Neurorehabilitation and neural repair, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hugh H ChanDepartment of Neurosciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.ORCID 0000-0002-9854-0229
Brittany M FisherDepartment of Neurosciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
Margaret A OimoenDepartment of Neurosciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
Latavya ChintadaDepartment of Neurosciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
Hemen KhannaDepartment of Neurosciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
Claire A SonnebornDepartment of Quantitative Health Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
Olivia HogueDepartment of Quantitative Health Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
André G MachadoNeurological Institute, Cleveland Clinic, Cleveland, OH, USA.
Kenneth B BakerDepartment of Neurosciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.

Funding

Deep Brain Stimulation of the Cerebellar Dentate Nucleus to Enhance Chronic, Post-Traumatic Brain Injury RehabilitationR01NS116384 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI BAKER, KENNETH B, MACHADO, ANDRE GUELMAN · 2020 to 2024
$2.5M
NINDS NIH HHS R01 NS116384
6 · The paper itself

Abstract

backgroundWe 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.

objectiveConsidering 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.

methodsHere, 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.

resultsTreated 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.

conclusionsLCN 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.

Indexed as

Brain Injuries, TraumaticDeep Brain StimulationDisease Models, AnimalRats, Long-EvansRecovery of FunctionAnimalsCerebellar NucleiMaleMotor ActivityNeuronal PlasticityRatsSensorimotor Cortexdeep brain stimulationlateral cerebellar nucleusmotor recoveryneuromodulationtraumatic brain injury

Identifiers

PMID39215643
PMCPMC11567800

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.