Evidence map›Paper›PMID 26425697›Full record

ArticleEBioMedicine2015

Astroglial Control of the Antidepressant-Like Effects of Prefrontal Cortex Deep Brain Stimulation.

A Etiévant, C Oosterhof, C Bétry, E Abrial, M Novo-Perez, R Rovera, H Scarna, C Devader, J Mazella, G Wegener and 8 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Biomarkers for Deep Brain Stimulation in Animal Models of Depression.Neuromodulation : journal of the International Neuromodulation Society · 2022
    Review
  13. Article
  14. Article
  15. Cortical astrocytes regulate ethanol consumption and intoxication in mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  16. Article
  17. Evidence-based complementary and alternative medicine : eCAM · 2021
    Article
  18. Review
  19. Article
  20. Neuroimmune signaling in alcohol use disorder.Pharmacology, biochemistry, and behavior · 2019
    Review
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

18 authors at 8 institutions in 4 countries.

A EtiévantStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France ; Department of Psychiatry and Neurosciences, Faculty of Medicine, Laval University-IUSMQ, Québec City, Québec, Canada.
C OosterhofInstitute of Mental Health Research, University of Ottawa, Ottawa, Ontario, Canada.
C BétryStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
E AbrialStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
M Novo-PerezStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
R RoveraStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
H ScarnaStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
C DevaderInstitut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, UMR6097, Université de Nice Sophia Antipolis, 06560 Valbonne, France.
J MazellaInstitut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, UMR6097, Université de Nice Sophia Antipolis, 06560 Valbonne, France.
G WegenerDepartment of Clinical Medicine, Translational Neuropsychiatry Unit, Aarhus University, Skovagervej 2, DK-8240 Risskov, Denmark.
C SánchezNeuropharmacology, Lundbeck Research USA, Paramus, NJ, USA.
O Dkhissi-BenyahyaStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
C GronfierStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
V CoizetINSERM U836, GIN, Univ. Grenoble Alpes, F-38000 Grenoble, France.
J M BeaulieuDepartment of Psychiatry and Neurosciences, Faculty of Medicine, Laval University-IUSMQ, Québec City, Québec, Canada.
P BlierInstitute of Mental Health Research, University of Ottawa, Ottawa, Ontario, Canada.
G LucasStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France ; Institut François Magendie, INSERM U862, Université de Bordeaux, 33077 Bordeaux, France.
N HaddjeriStem Cell and Brain Research Institute, INSERM U846, 69500 Bron, France ; Université de Lyon, Université Lyon 1, 69373 Lyon, France.
Institut Cellule Souche et Cerveau · FRUniversité Claude Bernard Lyon 1 · FRInserm · FRInstitut de Pharmacologie Moléculaire et Cellulaire · FRUniversity of Ottawa · CAAarhus University · DKLundbeck (Denmark) · DKUniversité Grenoble Alpes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although deep brain stimulation (DBS) shows promising efficacy as a therapy for intractable depression, the neurobiological bases underlying its therapeutic action remain largely unknown. The present study was aimed at characterizing the effects of infralimbic prefrontal cortex (IL-PFC) DBS on several pre-clinical markers of the antidepressant-like response and at investigating putative non-neuronal mechanism underlying DBS action. We found that DBS induced an antidepressant-like response that was prevented by IL-PFC neuronal lesion and by adenosine A1 receptor antagonists including caffeine. Moreover, high frequency DBS induced a rapid increase of hippocampal mitosis and reversed the effects of stress on hippocampal synaptic metaplasticity. In addition, DBS increased spontaneous IL-PFC low-frequency oscillations and both raphe 5-HT firing activity and synaptogenesis. Unambiguously, a local glial lesion counteracted all these neurobiological effects of DBS. Further in vivo electrophysiological results revealed that this astrocytic modulation of DBS involved adenosine A1 receptors and K(+) buffering system. Finally, a glial lesion within the site of stimulation failed to counteract the beneficial effects of low frequency (30 Hz) DBS. It is proposed that an unaltered neuronal-glial system constitutes a major prerequisite to optimize antidepressant DBS efficacy. It is also suggested that decreasing frequency could heighten antidepressant response of partial responders.

Indexed as

AstrocytesDeep Brain StimulationAnimalsDepressionMalePrefrontal CortexRatsRats, Sprague-DawleyAstrocytesDBS, deep brain stimulationDeep brain stimulationDepressionfEPSP, field excitatory post-synaptic potentialHFS, high frequency stimulationIL-PFC, infralimbic prefrontal cortexl-AAA, l-alpha-aminoadipic acidLFS, low frequency stimulationPCPA, 4-chloro-dl-phenylalanine methyl esterPrefrontal cortexSerotonin

Identifiers

PMID26425697
PMCPMC4563138
OpenAlexW2117187481

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.