Evidence map›Paper›PMID 25652922›Full record

ArticleJournal of neurophysiology2015

Pallidal stimulation suppresses pathological dysrhythmia in the parkinsonian motor cortex.

Kevin W McCairn, Robert S Turner

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Why so slow? Models of parkinsonian bradykinesia.Nature reviews. Neuroscience · 2024
    Review
  4. Dysfunction of motor cortices in Parkinson's disease.Cerebral cortex (New York, N.Y. : 1991) · 2024
    Review
  5. Review
  6. Frequency-Specific Optogenetic Deep Brain Stimulation of Subthalamic Nucleus Improves Parkinsonian Motor Behaviors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Deep Brain Stimulation for Movement Disorders of Basal Ganglia Origin: Restoring Function or Functionality?Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2016
    Review
  11. Mechanisms of deep brain stimulation.Journal of neurophysiology · 2016
    Review
  12. Review
  13. 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

2 authors at 2 institutions in 2 countries.

Kevin W McCairnDepartment of Neurological Surgery, University of California, San Francisco, California; Department of Biological Sciences, Milton Keynes, The Open University, Buckinghamshire, United Kingdom; and kevin.mccairn@yahoo.com.ORCID http://orcid.org/0000-0002-8546-4095
Robert S TurnerDepartment of Neurological Surgery, University of California, San Francisco, California; Department of Neurobiology and Center for the Neural Basis of Cognition, University of Pittsburgh, Pittsburgh, Pennsylvania.
University of California, San Francisco · USUniversity of Pittsburgh · US

Funding

Basal ganglia-thalamic signaling in parkinsonism and deep brain stimulationR01NS070865 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TURNER, ROBERT STERLING · 2011 to 2015
$1.8M
Surgery Core - NINDS Institutional Core Grants to Support Neuroscience ResearchP30NS076405 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STRICK, PETER · 2012 to 2016
$1.8M
DBS AND MOTOR CORTICAL FUNCTION IN AN MPTP MODEL OF PDR01NS044551 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TURNER, ROBERT STERLING · 2002 to 2006
$1.6M
NINDS NIH HHS 1P30-NS0-76405-01A1NINDS NIH HHS NS-044551NINDS NIH HHS NS-070865NINDS NIH HHS P30 NS076405NINDS NIH HHS R01 NS070865
6 · The paper itself

Abstract

Although there is general consensus that deep brain stimulation (DBS) yields substantial clinical benefit in patients with Parkinson's disease (PD), the therapeutic mechanism of DBS remains a matter of debate. Recent studies demonstrate that DBS targeting the globus pallidus internus (GPi-DBS) suppresses pathological oscillations in firing rate and between-cell spike synchrony in the vicinity of the electrode but has negligible effects on population-level firing rate or the prevalence of burst firing. The present investigation examines the downstream consequences of GPi-DBS at the level of the primary motor cortex (M1). Multielectrode, single cell recordings were conducted in the M1 of two parkinsonian nonhuman primates (Macaca fasicularis). GPi-DBS that induced significant reductions in muscular rigidity also reduced the prevalence of both beta (12-30 Hz) oscillations in single unit firing rates and of coherent spiking between pairs of M1 neurons. In individual neurons, GPi-DBS-induced increases in mean firing rate were three times more common than decreases; however, averaged across the population of M1 neurons, GPi-DBS induced no net change in mean firing rate. The population-level prevalence of burst firing was also not affected by GPi-DBS. The results are consistent with the hypothesis that suppression of both pathological, beta oscillations and synchronous activity throughout the cortico-basal ganglia network is a major therapeutic mechanism of GPi-DBS.

Indexed as

Deep Brain StimulationAction PotentialsAnimalsFemaleGlobus PallidusMacaca fascicularisMotor CortexNeuronsParkinsonian Disordersdeep brain stimulationglobus pallidusMPTPnonhuman primateParkinson's diseaseprimary motor cortex

Identifiers

PMID25652922
PMCPMC4416560
OpenAlexW2151111851

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.