Evidence map›Paper›PMID 17002597›Full record

ReviewAnnual review of pharmacology and toxicology2007

Contrasting actions of endothelin ET(A) and ET(B) receptors in cardiovascular disease.

Markus P Schneider, Erika I Boesen, David M Pollock

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of pharmacology and toxicology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed, 1 pooled it
5.9field-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

133 citing papers in PubMed, 1 synthesis or guideline pooled it, 288 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. bioRxiv : the preprint server for biology · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Endothelin-1 drives COX-2 and prostaglandin EJournal of dental sciences · 2026
    Article
  8. Combined Effects of Diosmin, Hesperidin,International journal of molecular sciences · 2025
    Article
  9. Dual ETFundamental & clinical pharmacology · 2025
    Article
  10. Review
  11. Article
  12. Review
  13. The MuCAYACJC open · 2024
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Sickle Cell Disease and CKD: An Update.American journal of nephrology · 2024
    Review
  20. Article

73 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Markus P SchneiderVascular Biology Center, Medical College of Georgia, Augusta, GA 30912, USA.
Erika I Boesen
David M Pollock
Augusta University · USLaboratoire d’immunologie intégrative du cancer · FR

Funding

Vascular Rho-kinase Signaling in Angiotensin II hypertenP01HL074167 · NHLBI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI POLLOCK, JENNIFER S · 2004 to 2008
$10.5M
ENDOTHELIN REGULATION OF KIDNEY FUNCTIONR01HL064776 · NHLBI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI POLLOCK, DAVID M · 2000 to 2007
$1.6M
NHLBI NIH HHS HL 64776NHLBI NIH HHS HL 74167NHLBI NIH HHS P01 HL074167NHLBI NIH HHS R01 HL064776
6 · The paper itself

Abstract

First identified as a powerful vasoconstrictor, endothelin has an extremely diverse set of actions that influence homeostatic mechanisms throughout the body. Two receptor subtypes, ET(A) and ET(B), which usually have opposing actions, mediate the actions of endothelin. ET(A) receptors function to promote vasoconstriction, growth, and inflammation, whereas ET(B) receptors produce vasodilation, increases in sodium excretion, and inhibit growth and inflammation. Potent and selective receptor antagonists have been developed and have shown promising results in the treatment of cardiovascular diseases such as pulmonary arterial hypertension, acute and chronic heart failure, hypertension, renal failure, and atherosclerosis. However, results are often contradictory and complicated because of the tissue-specific vasoconstrictor actions of ET(B) receptors and the fact that endothelin is an autocrine and paracrine factor whose activity is difficult to measure in vivo. Considerable questions remain regarding whether ET(A)-selective or nonselective ET(A)/ET(B) receptor antagonists would be useful in a range of clinical settings.

Indexed as

AnimalsCardiovascular DiseasesEndothelin A Receptor AntagonistsEndothelin B Receptor AntagonistsEndothelinsHumansReceptor, Endothelin AReceptor, Endothelin BEndothelin A Receptor AntagonistsEndothelin B Receptor AntagonistsEndothelinsReceptor, Endothelin AReceptor, Endothelin B

Identifiers

PMID17002597
PMCPMC2825895
OpenAlexW2110192403

What Socratic 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 Socratic graph.