Evidence map›Paper›PMID 14744803›Full record

ArticleBritish journal of pharmacology2004

Endothelins contribute towards nociception induced by antigen in ovalbumin-sensitised mice.

Anna P Piovezan, Pedro D'Orléans-Juste, Monica Frighetto, Glória E P Souza, Maria G M O Henriques, Giles A Rae

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-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

20 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Allergic Inflammation Leads to Neuropathic Pain via Glial Cell Activation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  5. Article
  6. Mast cells: versatile gatekeepers of pain.Molecular immunology · 2015
    Review
  7. Review
  8. An interleukin-33/ST2 signaling deficiency reduces overt pain-like behaviors in mice.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2013
    Article
  9. Article
  10. Article
  11. Mast cell degranulation mediates compound 48/80-induced hyperalgesia in mice.Biochemical and biophysical research communications · 2012
    Article
  12. Article
  13. Article
  14. Mechanism of cancer pain.Molecular interventions · 2010
    Review
  15. Article
  16. Article
  17. Article
  18. Endothelin receptors and pain.The journal of pain · 2009
    Review
  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

6 authors at 4 institutions in 2 countries.

Anna P PiovezanDepartment of Pharmacology, CCB, Universidade Federal de Santa Catarina, R Ferreira Lima 82, Florianópolis 88015-420, SC, Brazil.
Pedro D'Orléans-Juste
Monica Frighetto
Glória E P Souza
Maria G M O Henriques
Giles A Rae
Universidade Federal de Santa Catarina · BRFundação Oswaldo Cruz · BRUniversidade de Ribeirão Preto · BRUniversité de Sherbrooke · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. The contribution of endogenous endothelins to nociceptive responses elicited by ovalbumin (OVA) in the hind-paw of mice sensitised to this antigen (50 microg OVA+5 mg Al(OH)(3), s.c., 14 days beforehand) was investigated. 2. Sensitised mice exhibited greater nocifensive responsiveness to intraplantar (i.pl.) OVA (total licking time over first 30 min: 85.2+/-14.6 s at 0.3 microg; 152.6+/-35.6 s at 1 microg) than nonsensitised animals (29.3+/-7.4 s at 1 microg). Nocifensive responses of sensitised mice to 0.3 microg OVA were inhibited by morphine (3 mg kg(-1), s.c.) or local depletion of mast cells (four daily i.pl. injections of compound 48/80). 3. Pretreatment with i.v. bosentan (mixed ET(A)/ET(B) receptor antagonist; 52 micromol kg(-1)) or A-122722.5 (selective ET(A) receptor antagonist; 6 micromol kg(-1)) reduced OVA-induced licking from 124.8+/-20.6 s to 45.7+/-13.0 s and 64.2+/-12.1 s, respectively, whereas A-192621.1 (selective ET(B) receptor antagonist; 25 micromol kg(-1)) enhanced them to 259.2+/-39.6 s. 4. Local i.pl. pretreatment with BQ-123 or BQ-788 (selective ET(A) or ET(B) receptor antagonists, respectively, each at 3 nmol) reduced OVA-induced licking (from 106.2+/-15.2 to 57.0+/-9.4 s and from 118.6+/-10.5 to 76.8+/-14.7 s, respectively). Sarafotoxin S6c (selective ETB receptor agonist, 30 pmol, i.pl., 30 min after OVA) induced nocifensive responses in OVA-sensitised, but not in nonsensitised, animals. 5. Compound 48/80 (0.3 microg, i.pl.) induced nocifensive responses per se and potentiated those induced by i.pl. capsaicin (0.1 microg). Treatment with BQ-123 (3 nmol, i.pl.) reduced only the hyperalgesic effect of compound 48/80, whereas BQ-788 (3 nmol) was ineffective. 6. Thus, immune-mediated Type I hypersensitivity reactions elicit mast cell- and endothelin-dependent nociception in the mouse hind-paw, which are mediated locally by both ET(A) and ET(B) receptors. The nocifensive response to antigen is amenable to blockade by systemic treatment with dual ET(A)/ET(B) or selective ET(A) receptor antagonists, but is sharply potentiated by systemic selective ET(B) receptor antagonist treatment. The apparently distinct roles played by ET(B) receptors in this phenomenon at local and other sites remain to be characterised.

Indexed as

AnimalsAntigensBosentanDose-Response Relationship, DrugEndothelinsHyperalgesiaHypersensitivityIndicators and ReagentsMaleMiceOligopeptidesOvalbuminPainPeptides, CyclicPiperidinesp-Methoxy-N-methylphenethylamineAntigensBosentanBQ 788cyclo(Trp-Asp-Pro-Val-Leu)EndothelinsIndicators and ReagentsOligopeptidesOvalbuminPeptides, CyclicPiperidinesp-Methoxy-N-methylphenethylaminesarafotoxins s6SulfonamidesViper Venoms

Identifiers

PMID14744803
PMCPMC1574245
OpenAlexW2025819341

What OpenQuestion holds

Textmetadata
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.