Evidence map›Paper›PMID 18757499›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2008

Inflamed phenotype of the mesenteric microcirculation of melanocortin type 3 receptor-null mice after ischemia-reperfusion.

Giovanna Leoni, Hetal B Patel, André L F Sampaio, Felicity N E Gavins, Joanne F Murray, Paolo Grieco, Stephen J Getting, Mauro Perretti

Open access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2008. 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
2.4field-weighted citation impact, top 12% 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. Review
  2. Review
  3. Review
  4. Melanocortin Regulation of Inflammation.Frontiers in endocrinology · 2019
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Annexin A1 mediates hydrogen sulfide properties in the control of inflammation.The Journal of pharmacology and experimental therapeutics · 2014
    Article
  10. Article
  11. Article
  12. Control of myeloid cell trafficking in resolution.Journal of innate immunity · 2013
    Review
  13. Article
  14. Article
  15. Physiological roles of the melanocortin MC₃ receptor.European journal of pharmacology · 2011
    Review
  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

8 authors at 3 institutions in 2 countries.

Giovanna LeoniWilliam Harvey Research Institute, Barts and The London School of Medicine, Charterhouse Square, London, EC1M 6BQ, UK.
Hetal B Patel
André L F Sampaio
Felicity N E Gavins
Joanne F Murray
Paolo Grieco
Stephen J Getting
Mauro Perretti
William Harvey Research Institute · GBUniversity of Westminster · GBIstituto Nazionale di Fisica Nucleare, Sezione di Napoli · IT

Funding

British Heart Foundation FS/05/078/19406
6 · The paper itself

Abstract

The existence of anti-inflammatory circuits centered on melanocortin receptors (MCRs) has been supported by the inhibitory properties displayed by melanocortin peptides in models of inflammation and tissue injury. Here we addressed the pathophysiological effect that one MCR, MCR type 3 (MC3R), might have on vascular inflammation. After occlusion (35 min) and reopening of the superior mesenteric artery, MC3R-null mice displayed a higher degree of plasma extravasation (45 min postreperfusion) and cell adhesion and emigration (90 min postreperfusion). These cellular alterations were complemented by higher expression of mesenteric tissue CCL2 and CXCL1 (mRNA and protein) and myeloperoxydase, as compared with wild-type animals. MC1R and MC3R mRNA and protein were both expressed in the inflamed mesenteric tissue; however, no changes in vascular responses were observed in a mouse colony bearing an inactive MC1R. Pharmacological treatment of animals with a selective MC3R agonist ([D-Trp(8)]-gamma-melanocyte-stimulating hormone; 10 microg i.v.) produced marked attenuation of cell adhesion, emigration, and chemokine generation; such effects were absent in MC3R-null mice. These new data reveal the existence of a tonic inhibitory signal provided by MC3R in the mesenteric microcirculation of the mouse, acting to down-regulate cell trafficking and local mediator generation.

Indexed as

AnimalsCD11b AntigenCell AdhesionCell MovementChemokine CCL2Chemokine CXCL1Down-RegulationFrameshift MutationInflammationInflammation MediatorsL-SelectinMaleMelanocyte-Stimulating HormonesMesenteryMiceMicrocirculationCcl2 protein, mouseCD11b AntigenChemokine CCL2Chemokine CXCL1Cxcl1 protein, mousegamma-melanocyte-stimulating factor, Trp(8)-Inflammation MediatorsL-SelectinMelanocyte-Stimulating HormonesReceptor, Melanocortin, Type 3

Identifiers

PMID18757499
PMCPMC2700033
OpenAlexW2123111478

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.