Evidence map›Paper›PMID 39683782›Full record

ArticleMolecules (Basel, Switzerland)2024

Irisin Attenuates Neuroinflammation Targeting the NLRP3 Inflammasome.

Francesca Martina Filannino, Melania Ruggiero, Maria Antonietta Panaro, Dario Domenico Lofrumento, Teresa Trotta, Tarek Benameur, Antonia Cianciulli, Rosa Calvello, Federico Zoila, Chiara Porro

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. 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

10 authors.

Francesca Martina FilanninoDepartment of Clinical and Experimental Medicine, University of Foggia, I-71100 Foggia, Italy.ORCID 0000-0003-2399-3781
Melania RuggieroDepartment of Biosciences, Biotechnologies and Environment, University of Bari, I-70125 Bari, Italy.
Maria Antonietta PanaroDepartment of Biosciences, Biotechnologies and Environment, University of Bari, I-70125 Bari, Italy.ORCID 0000-0001-5457-1069
Dario Domenico LofrumentoDepartment of Biological and Environmental Sciences and Technologies, Section of Human Anatomy, University of Salento, I-73100 Lecce, Italy.ORCID 0000-0002-0106-3615
Teresa TrottaDepartment of Clinical and Experimental Medicine, University of Foggia, I-71100 Foggia, Italy.ORCID 0000-0001-5693-6172
Tarek BenameurDepartment of Biomedical Sciences, College of Medicine, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
Antonia CianciulliDepartment of Biosciences, Biotechnologies and Environment, University of Bari, I-70125 Bari, Italy.ORCID 0000-0002-9851-3124
Rosa CalvelloDepartment of Biosciences, Biotechnologies and Environment, University of Bari, I-70125 Bari, Italy.
Federico ZoilaDepartment of Clinical and Experimental Medicine, University of Foggia, I-71100 Foggia, Italy.
Chiara PorroDepartment of Clinical and Experimental Medicine, University of Foggia, I-71100 Foggia, Italy.ORCID 0000-0002-7526-6968

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroinflammation is defined as an immune response involving various cell types, particularly microglia, which monitor the neuroimmune axis. Microglia activate in two distinct ways: M1, which is pro-inflammatory and capable of inducing phagocytosis and releasing pro-inflammatory factors, and M2, which has anti-inflammatory properties. Inflammasomes are large protein complexes that form in response to internal danger signals, activating caspase-1 and leading to the release of pro-inflammatory cytokines such as interleukin 1β. Irisin, a peptide primarily released by muscles during exercise, was examined for its effects on BV2 microglial cells in vitro. Even at low concentrations, irisin was observed to influence the NLRP3 inflammasome, showing potential as a neuroprotective and anti-inflammatory agent after stimulation with lipopolysaccharides (LPSs). Irisin helped maintain microglia in their typical physiological state and reduced their migratory capacity. Irisin also increased Arg-1 protein expression, a marker of M2 polarization, while downregulating NLRP3, Pycard, caspase-1, IL-1β, and CD14. The results of this study indicate that irisin may serve as a crucial mediator of neuroprotection, thus representing an innovative tool for the prevention of neurodegenerative diseases.

Indexed as

FibronectinsInflammasomesLipopolysaccharidesMicrogliaNLR Family, Pyrin Domain-Containing 3 ProteinAnimalsAnti-Inflammatory AgentsCaspase 1Cell LineInterleukin-1betaMiceNeuroinflammatory DiseasesNeuroprotective AgentsAnti-Inflammatory AgentsCaspase 1FibronectinsFNDC5 protein, mouseInflammasomesInterleukin-1betaLipopolysaccharidesNeuroprotective AgentsNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseinflammasomeirisinmicroglianeuroinflammation

Identifiers

PMID39683782
PMCPMC11643767

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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.