Evidence map›Paper›PMID 36613574›Full record

ReviewInternational journal of molecular sciences2022

NLRP3 Inflammasome: From Pathophysiology to Therapeutic Target in Major Depressive Disorder.

Bruna R Kouba, Joana Gil-Mohapel, Ana Lúcia S Rodrigues

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. 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
2.4field-weighted citation impact, top 10% 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, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Differentiating Between Major Depressive Disorder and Bipolar Disorder.Advances in experimental medicine and biology · 2026
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 2 institutions in 2 countries.

Bruna R KoubaCenter of Biological Sciences, Department of Biochemistry, Universidade Federal de Santa Catarina, Florianópolis 88040-900, SC, Brazil.
Joana Gil-MohapelIsland Medical Program, Faculty of Medicine, University of British Columbia, Victoria, BC V8P 5C2, Canada.ORCID 0000-0003-4982-1662
Ana Lúcia S RodriguesCenter of Biological Sciences, Department of Biochemistry, Universidade Federal de Santa Catarina, Florianópolis 88040-900, SC, Brazil.
Universidade Federal de Santa Catarina · BRUniversity of British Columbia · CA

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior N/ANational Council for Scientific and Technological Development #3421142/2018-5University of Victoria (UVic, Victoria, BC, Canada) - São Paulo Research Foundation (FAPESP, São Paulo, SP, Brazil) SPRINT partnership UVic-FAPESP SPRINT 1/2018 Grant
6 · The paper itself

Abstract

Major depressive disorder (MDD) is a highly prevalent psychiatric disorder, whose pathophysiology has been linked to the neuroinflammatory process. The increased activity of the Nod-like receptor pyrin containing protein 3 (NLRP3) inflammasome, an intracellular multiprotein complex, is intrinsically implicated in neuroinflammation by promoting the maturation and release of proinflammatory cytokines such as interleukin (IL)-1β and IL-18. Interestingly, individuals suffering from MDD have higher expression of NLRP3 inflammasome components and proinflammatory cytokines when compared to healthy individuals. In part, intense activation of the inflammasome may be related to autophagic impairment. Noteworthy, some conventional antidepressants induce autophagy, resulting in less activation of the NLRP3 inflammasome. In addition, the fast-acting antidepressant ketamine, some bioactive compounds and physical exercise have also been shown to have anti-inflammatory properties via inflammasome inhibition. Therefore, it is suggested that modulation of inflammasome-driven pathways may have an antidepressant effect. Here, we review the role of the NLRP3 inflammasome in the pathogenesis of MDD, highlighting that pathways related to its priming and activation are potential therapeutic targets for the treatment of MDD.

Indexed as

InflammasomesMajor Depressive DisorderAntidepressive AgentsCytokinesHumansInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinAntidepressive AgentsCytokinesInflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 Proteinantidepressantsbioactive compoundsdepressionneuroinflammationNLRP3 complexphysical exercise

Identifiers

PMID36613574
PMCPMC9820112
OpenAlexW4312186750

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.