Evidence map›Paper›PMID 34279714›Full record

ReviewEuropean archives of psychiatry and clinical neuroscience2021

P2X7R antagonists in chronic stress-based depression models: a review.

Iven-Alex von Muecke-Heim, Clemens Ries, Lidia Urbina, Jan M Deussing

Open access · hybridAbstract readReview
In one paragraph

Review in European archives of psychiatry and clinical neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
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  12. Embers of the Past: Early Childhood Traumas Interact with Variation inInternational journal of molecular sciences · 2024
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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

4 authors at 2 institutions in 1 country.

Iven-Alex von Muecke-HeimMax Planck Institute of Psychiatry, Molecular Neurogenetics, Munich, Germany. iven_muecke-heim@psych.mpg.de.ORCID http://orcid.org/0000-0002-5021-9495
Clemens RiesMax Planck Institute of Psychiatry, Molecular Neurogenetics, Munich, Germany.
Lidia UrbinaMax Planck Institute of Psychiatry, Molecular Neurogenetics, Munich, Germany.
Jan M DeussingMax Planck Institute of Psychiatry, Molecular Neurogenetics, Munich, Germany. deussing@psych.mpg.de.ORCID http://orcid.org/0000-0002-9329-5252
Bernstein Center for Computational Neuroscience Munich · DEMax Planck Institute of Psychiatry · DE

Funding

Bundesministerium für Bildung und Forschung IMADAPT, FKZ: 01KU1901)Else Kröner-Fresenius-Stiftung IMPRS TP PhD Residency ProgramMax-Planck-Gesellschaft IMPRS-TP ProgrammMax-Planck-Gesellschaft IMPRS-TP Programm (minor funding)
6 · The paper itself

Abstract

Depression affects around 320 million people worldwide. Growing evidence proposes the immune system to be the core interface between psychosocial stress and the neurobiological and behavioural features of depression. Many studies have identified purinergic signalling via the P2X7 receptor (P2X7R) to be of great importance in depression genesis yet only a few have evaluated P2X7R antagonists in chronic stress-based depression models. This review summarizes their findings and analyses their methodology. The four available studies used three to nine weeks of unpredictable, chronic mild stress or unpredictable, chronic stress in male mice or rats. Stress paradigm composition varied moderately, with stimuli being primarily psychophysical rather than psychosocial. Behavioural testing was performed during or after the last week of stress application and resulted in depressive-like behaviours, immune changes (NLRP3 assembly, interleukin-1β level increase, microglia activation) and neuroplasticity impairment. During the second half of each stress paradigm, a P2X7R antagonist (Brilliant Blue G, A-438079, A-804598) was applied. Studies differed with regard to antagonist dosage and application timing. Nonetheless, all treatments attenuated the stress-induced neurobiological changes and depressive-like behaviours. The evidence at hand underpins the importance of P2X7R signalling in chronic stress and depression. However, improvements in study planning and reporting are necessary to minimize experimental bias and increase data purview. To achieve this, we propose adherence to the Research Domain Criteria and the STRANGE framework.

Indexed as

DepressionPurinergic P2X Receptor AntagonistsAnimalsChronic DiseaseDisease Models, AnimalMaleMiceRatsPurinergic P2X Receptor AntagonistsAnimal modelsChronic stressMicroglia and macrophagesP2X7R antagonistsP2X7 receptor (P2X7R)

Identifiers

PMID34279714
PMCPMC8429152
OpenAlexW3184040406

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.