Evidence map›Paper›PMID 12110609›Full record

ArticleBritish journal of pharmacology2002

P2Y(1) and P2Y(2) receptors are coupled to the NO/cGMP pathway to vasodilate the rat arterial mesenteric bed.

Sonja Buvinic, René Briones, J Pablo Huidobro-Toro

Abstract read
In one paragraph

Article in British journal of pharmacology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
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

49 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Intra-carotid body inter-cellular communication.Journal of the Royal Society of New Zealand · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. P2YFrontiers in pharmacology · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. P2Y receptors in Alzheimer's disease.Biology of the cell · 2015
    Review
  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

3 authors.

Sonja BuvinicCentro de Regulación Celular y Patología, Instituto Milenio de Biología Fundamental y Aplicada, MIFAB, Departamento de Fisiología, Unidad de Regulación Neurohumoral, Pontificia Universidad Católica de Chile, Casilla 114-D, Santiago 1, Chile.
René Briones
J Pablo Huidobro-Toro

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. To assess the role of nucleotide receptors in endothelial-smooth muscle signalling, changes in perfusion pressure of the rat arterial mesenteric bed, the luminal output of nitric oxide (NO) and guanosine 3',5' cyclic monophosphate (cGMP) accumulation were measured after the perfusion of nucleotides. 2. The rank order of potency of ATP and analogues in causing relaxation of precontracted mesenteries was: 2-MeSADP=2-MeSATP>ADP>ATP=UDP=UTP>adenosine. The vasodilatation was coupled to a concentration-dependent rise in NO and cGMP production. MRS 2179 selectively blocked the 2-MeSATP-induced vasodilatation, the NO surge and the cGMP accumulation, but not the UTP or ATP vasorelaxation. 3. mRNA encoding for P2Y(1), P2Y(2) and P2Y(6) receptors, but not the P2Y(4) receptor, was detected in intact mesenteries by RT-PCR. After endothelium removal, only P2Y(6) mRNA was found. 4. Endothelium removal or blockade of NO synthase obliterated the nucleotides-induced dilatation, the NO rise and cGMP accumulation. Furthermore, 2-MeSATP, ATP, UTP and UDP contracted endothelium-denuded mesenteries, revealing additional muscular P2Y and P2X receptors. 5. Blockade of soluble guanylyl cyclase reduced the 2-MeSATP and UTP-induced vasodilatation and the accumulation of cGMP without interfering with NO production. 6. Blockade of phosphodiesterases with IBMX increased 15-20 fold the 2-MeSATP and UTP-induced rise in cGMP; sildenafil only doubled the cGMP accumulation. A linear correlation between the rise in NO and cGMP was found. 7. Endothelial P2Y(1) and P2Y(2) receptors coupled to the NO/cGMP cascade suggest that extracellular nucleotides are involved in endothelial-smooth muscle signalling. Additional muscular P2Y and P2X receptors highlight the physiology of nucleotides in vascular regulation.

Indexed as

Signal TransductionAdenosine DiphosphateAnimalsCyclic GMPEndothelium, VascularGuanylate CyclaseHumansLuminescent MeasurementsMaleMesenteric ArteriesMuscle, Smooth, VascularNitric OxideNitric Oxide SynthaseNucleotidesPurinergic P2 Receptor AgonistsPurinergic P2 Receptor AntagonistsAdenosine DiphosphateCyclic GMPGuanylate CyclaseN(6)-methyl-2'-deoxyadenosine 3',5'-diphosphateNitric OxideNitric Oxide SynthaseNucleotidesP2RY1 protein, humanP2ry1 protein, ratP2RY2 protein, humanP2ry2 protein, ratPurinergic P2 Receptor AgonistsPurinergic P2 Receptor AntagonistsReceptors, Cytoplasmic and NuclearReceptors, Purinergic P2Receptors, Purinergic P2Y1Receptors, Purinergic P2Y2RNA, MessengerSoluble Guanylyl Cyclase

Identifiers

PMID12110609
PMCPMC1573418

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.