Evidence map›Paper›PMID 30905126›Full record

ArticleClinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology2019

Antidepressant-like Effects Induced by Chronic Blockade of the Purinergic 2X7 Receptor through Inhibition of Non-like Receptor Protein 1 Inflammasome in Chronic Unpredictable Mild Stress Model of Depression in Rats.

Feyza Aricioglu, Ceren Sahin Ozkartal, Tugce Bastaskin, Erdem Tüzün, Cansu Kandemir, Serap Sirvanci, Cem Ismail Kucukali, Tijen Utkan

Open access · diamondAbstract read
In one paragraph

Article in Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  9. Antidepressant-like effect of endogenous SONaunyn-Schmiedeberg's archives of pharmacology · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
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  16. P2X7R antagonists in chronic stress-based depression models: a review.European archives of psychiatry and clinical neuroscience · 2021
    Review
  17. Review
  18. Article
  19. Review
  20. Crosstalk Between ATP-PFrontiers in cellular 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

8 authors at 3 institutions in 1 country.

Feyza AriciogluDepartment of Pharmacology and Psychopharmacology Research Unit, Marmara University School of Pharmacy.
Ceren Sahin OzkartalDepartment of Pharmacology and Psychopharmacology Research Unit, Marmara University School of Pharmacy.
Tugce BastaskinDepartment of Pharmacology and Psychopharmacology Research Unit, Marmara University School of Pharmacy.
Erdem TüzünDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medical Research, Istanbul University.
Cansu KandemirDepartment of Histology and Embryology, Marmara University School of Medicine.
Serap SirvanciDepartment of Histology and Embryology, Marmara University School of Medicine.
Cem Ismail KucukaliDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medical Research, Istanbul University.
Tijen UtkanDepartment of Pharmacology, Kocaeli University School of Medicine.
Marmara University · TRIstanbul University · TRKocaeli Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePurinergic 2X7 receptor (P2X7R) activation is known to be involved in pathogenesis of depression. Our aims were to investigate P2X7R-activated inflammasome pathways in parallel with induction of depression and to test the antidepressant-like effects of the selective P2X7R antagonist Brilliant Blue G (BBG) in a rat model of chronic unpredictable mild stress (CUMS).

methodsMale Wistar albino rats were divided into control, CUMS, CUMS+BBG25 (25 mg/kg/day) and CUMS+BBG50 (50 mg/kg/day) groups (n=10 for each group). Various stressors were applied to rats for 6 weeks to establish the CUMS model and daily BBG treatment was started at the end of 3rd week. Sucrose preference test and forced swim test (FST) were performed to assess antidepressant-like effects. Brain samples were obtained for real-time polymerase chain reaction and immunohistochemistry analysis.

resultsIn FST, duration of immobility was reduced in the CUMS+BBG50 group. Also, BBG treatment significantly enhanced sucrose preference. While NLRP3 gene expression levels were unchanged in rats exposed to the CUMS protocol, expression levels of other inflammasome pathway factors NLRP1, caspase-1, ASC, NF-κB, IL-1β, IL-6 and P2X7R were increased. BBG treatment reduced expression levels of these factors. Likewise, Iba-1 and GFAP immunoreactivities were enhanced by the CUMS protocol and this action was reversed by BBG treatment.

conclusionChronic administration of BBG in CUMS model results in antidepressant-like activity in a dose dependent manner. Molecular and histological results show that these effects might be at least partially related to the suppression of inflammasome-related neuroinflammatory responses and suggest involvement of NLRP1 in depression.

Indexed as

Animal modelsATP receptorCoomassie Brilliant BlueDepressionPurinergic P2X7 receptors

Identifiers

PMID30905126
PMCPMC6478084
OpenAlexW2921902092

What OpenQuestion holds

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Registered trials

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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.