Evidence map›Paper›PMID 21606476›Full record

ArticleThorax2011

EP4 receptor as a new target for bronchodilator therapy.

James Buckley, Mark A Birrell, Sarah A Maher, Anthony T Nials, Deborah L Clarke, Maria G Belvisi

Open access · hybridAbstract read
In one paragraph

Article in Thorax, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Pulmonary surfactant and prostaglandin EPhysiological reports · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Can GPCRs Be Targeted to Control Inflammation in Asthma?Advances in experimental medicine and biology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Transient receptor potential ankyrin-1 causes rapid bronchodilation via nonepithelial PGEAmerican journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  18. Review
  19. Bronchodilation induced by PGEBritish journal of pharmacology · 2020
    Article
  20. 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

6 authors at 2 institutions in 1 country.

James BuckleyRespiratory Pharmacology, Pharmacology and Toxicology Section, Imperial College London, Faculty of Medicine, National Heart and Lung Institute, Sir Alexander Fleming Building, London SW7 2AZ, UK.
Mark A Birrell
Sarah A Maher
Anthony T Nials
Deborah L Clarke
Maria G Belvisi
Imperial College London · GBGlaxoSmithKline (United Kingdom) · GB

Funding

Biotechnology and Biological Sciences Research Council BB/E52708X/1Medical Research Council G0502019Medical Research Council G0800195Medical Research Council G0800196
6 · The paper itself

Abstract

backgroundAsthma and chronic obstructive pulmonary disease are airway inflammatory diseases characterised by airflow obstruction. Currently approved bronchodilators such as long-acting β(2) adrenoceptor agonists are the mainstay treatments but often fail to relieve symptoms of chronic obstructive pulmonary disease and severe asthma and safety concerns have been raised over long-term use. The aim of the study was to identify the receptor involved in prostaglandin E(2) (PGE(2))-induced relaxation in guinea pig, murine, monkey, rat and human airways in vitro.

methodsUsing an extensive range of pharmacological tools, the relaxant potential of PGE(2) and selective agonists for the EP(1-4) receptors in the presence and absence of selective antagonists in guinea pig, murine, monkey, rat and human isolated airways was investigated.

resultsIn agreement with previous studies, it was found that the EP(2) receptor mediates PGE(2)-induced relaxation of guinea pig, murine and monkey trachea and that the EP(4) receptor mediates PGE(2)-induced relaxation of the rat trachea. These data have been confirmed in murine airways from EP(2) receptor-deficient mice (Ptger2). In contrast to previous publications, a role for the EP(4) receptor in relaxant responses in human airways in vitro was found. Relaxant activity of AH13205 (EP(2) agonist) was also demonstrated in guinea pig but not human airway tissue, which may explain its failure in clinical studies.

conclusionIdentification of the receptor mediating PGE(2)-induced relaxation represents a key step in developing a novel bronchodilator therapy. These data explain the lack of bronchodilator activity observed with selective EP(2) receptor agonists in clinical studies.

Indexed as

AlprostadilAnimalsAsthmaBridged Bicyclo Compounds, HeterocyclicBronchodilator AgentsDinoprostoneFatty Acids, UnsaturatedGuinea PigsHumansHydrazinesMacaca fascicularisMethyl EthersMiceMice, Inbred C57BLNaphthalenesPhenylbutyrates4-(4-cyano-2-(2-(4-fluoronaphthalen-1-yl)propionylamino)phenyl)butyric acid6-isopropoxy-9-oxoxanthene-2-carboxylic acid9-deoxy-9-chloro-15-deoxy-16-hydroxy-17,17-trimethylene-19,20-didehydroprostaglandin E2AH 13205AlprostadilBridged Bicyclo Compounds, HeterocyclicBronchodilator AgentsDinoprostoneFatty Acids, UnsaturatedHydrazinesMethyl EthersNaphthalenesONO-AE1-329ONO AE 248ONO-DI-004PhenylbutyratesProstanoic AcidsReceptors, Prostaglandin ESQ 29548Xanthones

Identifiers

PMID21606476
PMCPMC3221321
OpenAlexW2171568094

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.