Evidence map›Paper›PMID 15483626›Full record

ArticleThe EMBO journal2004

IRAG is essential for relaxation of receptor-triggered smooth muscle contraction by cGMP kinase.

Angela Geiselhöringer, Matthias Werner, Katja Sigl, Petra Smital, René Wörner, Linda Acheo, Juliane Stieber, Pascal Weinmeister, Robert Feil, Susanne Feil and 3 more

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 135 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The machinery of healthy vasodilatation: an overview.Pflugers Archiv : European journal of physiology · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Novel Functional Features of cGMP Substrate Proteins IRAG1 and IRAG2.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Function of IRAG2 Is Modulated by NO/cGMP in Murine Platelets.International journal of molecular sciences · 2022
    Article
  11. Review
  12. Review
  13. CaAdvances in experimental medicine and biology · 2022
    Article
  14. Review
  15. IRAG2 Interacts with IPInternational journal of molecular sciences · 2021
    Article
  16. Nitric Oxide: From Gastric Motility to Gastric Dysmotility.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Review
  19. Loss of PKGIβ/IRAG1 Signaling Causes Anemia-Associated Splenomegaly.International journal of molecular sciences · 2021
    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

13 authors at 1 institution in 1 country.

Angela GeiselhöringerInstitut für Pharmakologie und Toxikologie, Technische Universität München, Biedersteiner Strasse 29, 80802 München, Germany.
Matthias Werner
Katja Sigl
Petra Smital
René Wörner
Linda Acheo
Juliane Stieber
Pascal Weinmeister
Robert Feil
Susanne Feil
Jörg Wegener
Franz Hofmann
Jens Schlossmann
Technical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signalling by cGMP-dependent protein kinase type I (cGKI) relaxes various smooth muscles modulating thereby vascular tone and gastrointestinal motility. cGKI-dependent relaxation is possibly mediated by phosphorylation of the inositol 1,4,5-trisphosphate receptor I (IP(3)RI)-associated protein (IRAG), which decreases hormone-induced IP(3)-dependent Ca(2+) release. We show now that the targeted deletion of exon 12 of IRAG coding for the N-terminus of the coiled-coil domain disrupted in vivo the IRAG-IP(3)RI interaction and resulted in hypomorphic IRAG(Delta12/Delta12) mice. These mice had a dilated gastrointestinal tract and a disturbed gastrointestinal motility. Carbachol- and phenylephrine-contracted smooth muscle strips from colon and aorta, respectively, of IRAG(Delta12/Delta12) mice were not relaxed by cGMP, while cAMP-mediated relaxation was unperturbed. Norepinephrine-induced increases in [Ca(2+)](i) were not decreased by cGMP in aortic smooth muscle cells from IRAG(Delta12/Delta12) mice. In contrast, cGMP-induced relaxation of potassium-induced smooth muscle contraction was not abolished in IRAG(Delta12/Delta12) mice. We conclude that cGMP-dependent relaxation of hormone receptor-triggered smooth muscle contraction essentially depends on the interaction of cGKI-IRAG with IP(3)RI.

Indexed as

PhosphoproteinsAnimalsAortaCalciumCarbacholChlorocebus aethiopsCholinergic AgonistsColonCOS CellsCyclic GMPCyclic GMP-Dependent Protein KinasesExonsGadoliniumGastrointestinal MotilityGastrointestinal TractGene Targeting8-bromocyclic GMPCalciumCarbacholCholinergic AgonistsCyclic GMPCyclic GMP-Dependent Protein KinasesGadoliniumMembrane ProteinsMrvi1 protein, mousePhosphoproteins

Identifiers

PMID15483626
PMCPMC524403
OpenAlexW2125590987

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.