Evidence map›Paper›PMID 19922540›Full record

ArticleBritish journal of pharmacology2009

Characterization of biosynthesis and modes of action of prostaglandin E2 and prostacyclin in guinea pig mesenteric lymphatic vessels.

Sonia Rehal, Pauline Blanckaert, Simon Roizes, Pierre-Yves von der Weid

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

21 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. KAmerican journal of physiology. Cell physiology · 2022
    Review
  3. Article
  4. Review
  5. Renal lymphatic vessel dynamics.American journal of physiology. Renal physiology · 2020
    Article
  6. Article
  7. Review
  8. Inflammation and Lymphatic Function.Frontiers in immunology · 2019
    Review
  9. Review
  10. Article
  11. Lymph vessels: the forgotten second circulation in health and disease.Virchows Archiv : an international journal of pathology · 2016
    Review
  12. Article
  13. Mesenteric lymphatic vessels adapt to mesenteric venous hypertension by becoming weaker pumps.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Article
  14. Review
  15. Itching for answers: how histamine relaxes lymphatic vessels.Microcirculation (New York, N.Y. : 1994) · 2014
    Article
  16. Article
  17. Review
  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

4 authors at 2 institutions in 1 country.

Sonia RehalSnyder Institute of Infection, Immunity & Inflammation and Libin Cardiovascular Institute of Alberta, Calgary, Alberta, Canada.
Pauline Blanckaert
Simon Roizes
Pierre-Yves von der Weid
Libin Cardiovascular Institute of Alberta · CAUniversity of Calgary · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

background and purposeRhythmical transient constrictions of the lymphatic vessels provide the means for efficient lymph drainage and interstitial tissue fluid balance. This activity is critical during inflammation, to avoid or limit oedema resulting from increased vascular permeability, mediated by the release of various inflammatory mediators. In this study, we investigated the mechanisms by which prostaglandin E(2) (PGE(2)) and prostacyclin modulate lymphatic contractility in isolated guinea pig mesenteric lymphatic vessels. EXPERIMENTAL APPROACH: Quantitative RT-PCR was used to assess the expression of mRNA for enzymes and receptors involved in the production and action of PGE(2) and prostacyclin in mesenteric collecting lymphatic vessels. Frequency and amplitude of lymphatic vessel constriction were measured in the presence of these prostaglandins and the role of their respective EP and IP receptors assessed. KEY

resultsProstaglandin E(2) and prostacyclin decreased concentration-dependently the frequency, without affecting the amplitude, of lymphatic constriction. Data obtained in the presence of the EP(4) receptor antagonists, GW627368x (1 microM) and AH23848B (30 microM) and the IP receptor antagonist CAY10441 (0.1 microM) suggest that PGE(2) predominantly activates EP(4), whereas prostacyclin mainly stimulates IP receptors. Inhibition of responses to either prostaglandin with H89 (10 microM) or glibenclamide (1 microM) suggested a role for the activation of protein kinase A and ATP-sensitive K(+) channels. CONCLUSIONS AND IMPLICATIONS: Our findings characterized the inhibition of lymphatic pumping induced by PGE(2) or prostacyclin in guinea pig mesenteric lymphatics. This action is likely to impair oedema resolution and to contribute to the pro-inflammatory actions of these prostaglandins.

Indexed as

AnimalsDinoprostoneDose-Response Relationship, DrugEdemaEpoprostenolGuinea PigsLymphatic VesselsMaleMesenteryMuscle ContractionReceptors, EpoprostenolReceptors, Prostaglandin EReceptors, Prostaglandin E, EP4 SubtypeReverse Transcriptase Polymerase Chain ReactionRNA, MessengerDinoprostoneEpoprostenolReceptors, EpoprostenolReceptors, Prostaglandin EReceptors, Prostaglandin E, EP4 SubtypeRNA, Messenger

Identifiers

PMID19922540
PMCPMC2807658
OpenAlexW1512706072

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.