Evidence map›Paper›PMID 31174279›Full record

ReviewInternational journal of molecular sciences2019

P2X7 Receptor Signaling in Stress and Depression.

Deidiane Elisa Ribeiro, Aline Lulho Roncalho, Talita Glaser, Henning Ulrich, Gregers Wegener, Sâmia Joca

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
9.6field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

11 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Deidiane Elisa RibeiroDepartment of Biochemistry, Chemistry Institute, University of Sao Paulo, Sao Paulo SP 05508-000, Brazil. deidiane@hotmail.com.ORCID 0000-0002-3850-4867
Aline Lulho RoncalhoDepartment of Pharmacology, School of Medicine of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto 14049-900, Brazil. aline.roncalho@gmail.com.
Talita GlaserDepartment of Biochemistry, Chemistry Institute, University of Sao Paulo, Sao Paulo SP 05508-000, Brazil. tali.gla@gmail.com.
Henning UlrichDepartment of Biochemistry, Chemistry Institute, University of Sao Paulo, Sao Paulo SP 05508-000, Brazil. henning@iq.usp.br.
Gregers WegenerTranslational Neuropsychiatry Unit (TNU), Department of Clinical Medicine, Aarhus University, DK-8240 Risskov, Denmark. wegener@clin.au.dk.
Sâmia JocaDepartment of Physics and Chemistry, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto 14040-903, Brazil. sjoca@aias.au.dk.ORCID 0000-0003-0255-5889
Universidade de São Paulo · BRAarhus University · DK

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 304780/2018-9Danmarks Frie Forskningsfond 8020-00310BFundação de Amparo à Pesquisa do Estado de São Paulo 2015/13345-1; 2012/50880-4; 2018/08426-0Horizon 2020 754513
6 · The paper itself

Abstract

Stress exposure is considered to be the main environmental cause associated with the development of depression. Due to the limitations of currently available antidepressants, a search for new pharmacological targets for treatment of depression is required. Recent studies suggest that adenosine triphosphate (ATP)-mediated signaling through the P2X7 receptor (P2X7R) might play a prominent role in regulating depression-related pathology, such as synaptic plasticity, neuronal degeneration, as well as changes in cognitive and behavioral functions. P2X7R is an ATP-gated cation channel localized in different cell types in the central nervous system (CNS), playing a crucial role in neuron-glia signaling. P2X7R may modulate the release of several neurotransmitters, including monoamines, nitric oxide (NO) and glutamate. Moreover, P2X7R stimulation in microglia modulates the innate immune response by activating the NLR family pyrin domain containing 3 (NLRP3) inflammasome, consistent with the neuroimmune hypothesis of MDD. Importantly, blockade of P2X7R leads to antidepressant-like effects in different animal models, which corroborates the findings that the gene encoding for the P2X7R is located in a susceptibility locus of relevance to depression in humans. This review will discuss recent findings linked to the P2X7R involvement in stress and MDD neuropathophysiology, with special emphasis on neurochemical, neuroimmune, and neuroplastic mechanisms.

Indexed as

Signal TransductionAnimalsBrainDepressionHumansNeurotransmitter AgentsNLR Family, Pyrin Domain-Containing 3 ProteinReceptors, Purinergic P2X7Stress, PsychologicalNeurotransmitter AgentsNLR Family, Pyrin Domain-Containing 3 ProteinReceptors, Purinergic P2X7depressionneuroinflammationP2X7 receptorstress

Identifiers

PMID31174279
PMCPMC6600521
OpenAlexW2948329699

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.