Evidence map›Paper›PMID 20307668›Full record

ArticleNeurobiology of disease2010

Stimulation of the rat subthalamic nucleus is neuroprotective following significant nigral dopamine neuron loss.

A L Spieles-Engemann, M M Behbehani, T J Collier, S L Wohlgenant, K Steece-Collier, K Paumier, B F Daley, S Gombash, L Madhavan, G T Mandybur and 3 more

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of disease, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 3 pooled it
5.7field-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

60 citing papers in PubMed, 3 syntheses or guidelines pooled it, 133 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Deep brain stimulation for early-stage Parkinson's disease: an illustrative case.Neuromodulation : journal of the International Neuromodulation Society
    Trial
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Neuroprotection and Non-Invasive Brain Stimulation: Facts or Fiction?International journal of molecular sciences · 2022
    Review
  16. How Does Deep Brain Stimulation Change the Course of Parkinson's Disease?Movement disorders : official journal of the Movement Disorder Society · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. Striatal Afferent BDNF Is Disrupted by Synucleinopathy and Partially Restored by STN DBS.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    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

13 authors at 1 institution in 1 country.

A L Spieles-EngemannDepartment of Neurology, University of Cincinnati, Cincinnati, OH 45267, USA.
M M Behbehani
T J Collier
S L Wohlgenant
K Steece-Collier
K Paumier
B F Daley
S Gombash
L Madhavan
G T Mandybur
J W Lipton
B T Terpstra
C E Sortwell
University of Cincinnati · US

Funding

STN Deep Brain Stimulation and NeuroprotectionP50NS058830 · NINDS · UNIVERSITY OF CINCINNATI · PI COLLIER, TIMOTHY J. · 2009 to 2015
$5.9M
The Neuroprotective Effects of HF STN-DBSF31NS064696 · NINDS · UNIVERSITY OF CINCINNATI · PI ENGEMANN, ANNE · 2009 to 2010
$59k
NINDS NIH HHS F31 NS064696NINDS NIH HHS NS058830NINDS NIH HHS NS064696NINDS NIH HHS P50 NS058830
6 · The paper itself

Abstract

Deep brain stimulation of the subthalamic nucleus (STN-DBS) is efficacious in treating the motor symptoms of Parkinson's disease (PD). However, the impact of STN-DBS on the progression of PD is unknown. Previous preclinical studies have demonstrated that STN-DBS can attenuate the degeneration of a relatively intact nigrostriatal system from dopamine (DA)-depleting neurotoxins. The present study examined whether STN-DBS can provide neuroprotection in the face of prior significant nigral DA neuron loss similar to PD patients at the time of diagnosis. STN-DBS between 2 and 4 weeks after intrastriatal 6-hydroxydopamine (6-OHDA) provided significant sparing of DA neurons in the SN of rats. This effect was not due to inadvertent lesioning of the STN and was dependent upon proper electrode placement. Since STN-DBS appears to have significant neuroprotective properties, initiation of STN-DBS earlier in the course of PD may provide added neuroprotective benefits in addition to its ability to provide symptomatic relief.

Indexed as

AnimalsCell DeathCytoprotectionDeep Brain StimulationDisease Models, AnimalDopamineMaleNerve DegenerationNeural InhibitionParkinsonian DisordersRatsRats, Sprague-DawleySubstantia NigraSubthalamic NucleusTreatment OutcomeDopamine

Identifiers

PMID20307668
PMCPMC2879040
OpenAlexW2091078081

What OpenQuestion holds

Textmetadata
LicenceTDM
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.