Evidence map›Paper›PMID 37816600›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2023

Selective Activation of Subthalamic Nucleus Output Quantitatively Scales Movements.

Alexander D Friedman, Henry H Yin

Open access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Role of the subthalamic nucleus in motor control.Neural regeneration research · 2026
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  7. Stopping Muscle Contractions and Relaxations during Action Inhibition Involves Global and Targeted Control Dependent on Muscle State.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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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

2 authors at 1 institution in 1 country.

Alexander D FriedmanDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina 27708.
Henry H YinDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina 27708 hy43@duke.edu.
Duke University · US

Funding

The Role of Opponent Basal Ganglia Outputs in BehaviorR01NS094754 · NINDS · DUKE UNIVERSITY · PI Henry Yin · 2017 to 2026
$3.7M
The Role of Parafascicular Thalamic Circuits in Action GenerationR01NS121253 · NINDS · DUKE UNIVERSITY · PI YIN, HENRY · 2021 to 2025
$2.0M
Striatal Circuits for Goal PursuitR01MH112883 · NIMH · DUKE UNIVERSITY · PI YIN, HENRY · 2017 to 2021
$1.6M
NIMH NIH HHS R01 MH112883NINDS NIH HHS R01 NS094754NINDS NIH HHS R01 NS121253
6 · The paper itself

Abstract

The subthalamic nucleus (STN) is a common target for deep brain stimulation (DBS) treatments of Parkinsonian motor symptoms. According to the dominant model, the STN output can suppress movement by enhancing inhibitory basal ganglia (BG) output via the indirect pathway, and disrupting STN output using DBS can restore movement in Parkinson's patients. But the mechanisms underlying STN DBS remain poorly understood, as previous studies usually relied on electrical stimulation, which cannot selectively target STN output neurons. Here, we selectively stimulated STN projection neurons using optogenetics and quantified behavior in male and female mice using 3D motion capture. STN stimulation resulted in movements with short latencies (10-15 ms). A single pulse of light was sufficient to generate movement, and there was a highly linear relationship between stimulation frequency and kinematic measures. Unilateral stimulation caused movement in the ipsiversive direction (toward the side of stimulation) and quantitatively determined head yaw and head roll, while stimulation of either STN raises the head (pitch). Bilateral stimulation does not cause turning but raised the head twice as high as unilateral stimulation of either STN. Optogenetic stimulation increased the firing rate of STN neurons in a frequency-dependent manner, and the increased firing is responsible for stimulation-induced movements. Finally, stimulation of the STN's projection to the brainstem mesencephalic locomotor region was sufficient to reproduce the behavioral effects of STN stimulation. These results question the common assumption that the STN suppresses movement, and instead suggest that STN output can precisely specify action parameters via direct projections to the brainstem.

Indexed as

Deep Brain StimulationParkinsonian DisordersSubthalamic NucleusAnimalsBasal GangliaFemaleHumansMaleMiceMovementbasal gangliadeep brain stimulationkinematicsmovementoptogeneticssubthalamic nucleus

Identifiers

PMID37816600
PMCPMC10669786
OpenAlexW4387492774

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.