Evidence map›Paper›PMID 27582298›Full record

ArticleJournal of neurophysiology2016

Robust modulation of arousal regulation, performance, and frontostriatal activity through central thalamic deep brain stimulation in healthy nonhuman primates.

Jonathan L Baker, Jae-Wook Ryou, Xuefeng F Wei, Christopher R Butson, Nicholas D Schiff, Keith P Purpura

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% of its field
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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

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  20. The Arousal-Related "Central Thalamus" Stimulation Site Simultaneously Innervates Multiple High-Level Frontal and Parietal Areas.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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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

6 authors at 5 institutions in 1 country.

Jonathan L BakerFeil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, New York; job2037@med.cornell.edu.
Jae-Wook RyouFeil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, New York.
Xuefeng F WeiCollege of New Jersey, Department of Biomedical Engineering, Ewing Township, New Jersey; and.
Christopher R ButsonUniversity of Utah, Scientific Computing & Imaging (SCI) Institute, Department of Bioengineering, Salt Lake City, Utah.
Nicholas D SchiffFeil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, New York.
Keith P PurpuraFeil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, New York.
Cornell University · USCollege of New Jersey · USMIND Research Institute · USUniversity of Utah · USWeill Cornell Medicine · US

Funding

TRD - VisualizationP41GM103545 · NIGMS · UNIVERSITY OF UTAH · PI JURRUS, ELIZABETH · 2012 to 2019
$9.7M
CENTRAL THALAMIC DEEP BRAIN STIMULATION MODELSR01NS067249 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BUTSON, CHRISTOPHER R, PFAFF, DONALD W. · 2009 to 2013
$3.2M
NIGMS NIH HHS P41 GM103545NINDS NIH HHS R01 NS067249
6 · The paper itself

Abstract

The central thalamus (CT) is a key component of the brain-wide network underlying arousal regulation and sensory-motor integration during wakefulness in the mammalian brain. Dysfunction of the CT, typically a result of severe brain injury (SBI), leads to long-lasting impairments in arousal regulation and subsequent deficits in cognition. Central thalamic deep brain stimulation (CT-DBS) is proposed as a therapy to reestablish and maintain arousal regulation to improve cognition in select SBI patients. However, a mechanistic understanding of CT-DBS and an optimal method of implementing this promising therapy are unknown. Here we demonstrate in two healthy nonhuman primates (NHPs), Macaca mulatta, that location-specific CT-DBS improves performance in visuomotor tasks and is associated with physiological effects consistent with enhancement of endogenous arousal. Specifically, CT-DBS within the lateral wing of the central lateral nucleus and the surrounding medial dorsal thalamic tegmental tract (DTTm) produces a rapid and robust modulation of performance and arousal, as measured by neuronal activity in the frontal cortex and striatum. Notably, the most robust and reliable behavioral and physiological responses resulted when we implemented a novel method of CT-DBS that orients and shapes the electric field within the DTTm using spatially separated DBS leads. Collectively, our results demonstrate that selective activation within the DTTm of the CT robustly regulates endogenous arousal and enhances cognitive performance in the intact NHP; these findings provide insights into the mechanism of CT-DBS and further support the development of CT-DBS as a therapy for reestablishing arousal regulation to support cognition in SBI patients.

Indexed as

AnimalsArousalCorpus StriatumDeep Brain StimulationFrontal LobeMacaca mulattaNeural PathwaysPsychomotor PerformanceReaction TimeThalamusarousal regulationcentral thalamusdeep brain stimulationintralaminar nucleisevere brain injury

Identifiers

PMID27582298
PMCPMC5116485
OpenAlexW2514213849

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.