Evidence map›Paper›PMID 25517119›Full record

ArticlePloS one2014

Formyl peptide receptor as a novel therapeutic target for anxiety-related disorders.

Irene Gallo, Lorenza Rattazzi, Giuseppa Piras, Thomas Gobbetti, Elisabetta Panza, Mauro Perretti, Jeffrey W Dalley, Fulvio D'Acquisto

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  6. Review
  7. Review
  8. Behavioral changes inFrontiers in neuroscience · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Microglial IRF5-IRF4 regulatory axis regulates neuroinflammation after cerebral ischemia and impacts stroke outcomes.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Review
  16. Review
  17. Review
  18. Chemotactic Ligands that Activate G-Protein-Coupled Formylpeptide Receptors.International journal of molecular sciences · 2019
    Review
  19. Article
  20. Oxyma-based phosphates for racemization-free peptide segment couplings.Journal of peptide science : an official publication of the European Peptide Society · 2016
    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 4 institutions in 2 countries.

Irene GalloWilliam Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.
Lorenza RattazziWilliam Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.
Giuseppa PirasWilliam Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.
Thomas GobbettiWilliam Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.
Elisabetta PanzaDepartment of Experimental Pharmacology, University of Naples "Federico II", Naples, Italy.
Mauro PerrettiWilliam Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.
Jeffrey W DalleyDepartment of Psychology, University of Cambridge, Cambridge, United Kingdom; Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Fulvio D'AcquistoWilliam Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.
William Harvey Research Institute · GBQueen Mary University of London · GBUniversity of Cambridge · GBUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formyl peptide receptors (FPR) belong to a family of sensors of the immune system that detect microbe-associated molecules and inform various cellular and sensorial mechanisms to the presence of pathogens in the host. Here we demonstrate that Fpr2/3-deficient mice show a distinct profile of behaviour characterised by reduced anxiety in the marble burying and light-dark box paradigms, increased exploratory behaviour in an open-field, together with superior performance on a novel object recognition test. Pharmacological blockade with a formyl peptide receptor antagonist, Boc2, in wild type mice reproduced most of the behavioural changes observed in the Fpr2/3(-/-) mice, including a significant improvement in novel object discrimination and reduced anxiety in a light/dark shuttle test. These effects were associated with reduced FPR signalling in the gut as shown by the significant reduction in the levels of p-p38. Collectively, these findings suggest that homeostatic FPR signalling exerts a modulatory effect on anxiety-like behaviours. These findings thus suggest that therapies targeting FPRs may be a novel approach to ameliorate behavioural abnormalities present in neuropsychiatric disorders at the cognitive-emotional interface.

Indexed as

Molecular Targeted TherapyAnimalsAnxietyCorticosteroneExploratory BehaviorGene DeletionMaleMiceNervous System DiseasesOligopeptidesReceptors, Formyl PeptideRecognition, PsychologySignal Transductionbutyloxycarbonyl-phenylalanyl-leucyl-phenylalanyl-leucyl-phenylalanineCorticosteroneOligopeptidesReceptors, Formyl Peptide

Identifiers

PMID25517119
PMCPMC4269406
OpenAlexW2093155447

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.