Evidence map›Paper›PMID 30217073›Full record

ArticleInternational journal of molecular sciences2018

Endothelial AMP-Activated Kinase α1 Phosphorylates eNOS on Thr495 and Decreases Endothelial NO Formation.

Nina Zippel, Annemarieke E Loot, Heike Stingl, Voahanginirina Randriamboavonjy, Ingrid Fleming, Beate Fisslthaler

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Apelin/APJ system: an emerging therapeutic target for respiratory diseases.Cellular and molecular life sciences : CMLS · 2020
    Review
  11. Review
  12. The Roles of AMPK in Revascularization.Cardiology research and practice · 2020
    Review
  13. Article
  14. AMP-Activated Protein Kinase Signalling.International journal of molecular sciences · 2019
    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

6 authors at 1 institution in 1 country.

Nina ZippelInstitute for Vascular Signalling, Centre for Molecular Medicine, Johann Wolfgang Goethe University, 60590 Frankfurt, Germany. NZippel@gmx.de.
Annemarieke E LootInstitute for Vascular Signalling, Centre for Molecular Medicine, Johann Wolfgang Goethe University, 60590 Frankfurt, Germany. a.loot@certe.nl.
Heike StinglInstitute for Vascular Signalling, Centre for Molecular Medicine, Johann Wolfgang Goethe University, 60590 Frankfurt, Germany. Stingl@vrc.uni-frankfurt.de.
Voahanginirina RandriamboavonjyInstitute for Vascular Signalling, Centre for Molecular Medicine, Johann Wolfgang Goethe University, 60590 Frankfurt, Germany. Voahangy@vrc.uni-frankfurt.de.
Ingrid FlemingInstitute for Vascular Signalling, Centre for Molecular Medicine, Johann Wolfgang Goethe University, 60590 Frankfurt, Germany. fleming@em.uni-frankfurt.de.ORCID 0000-0003-1881-3635
Beate FisslthalerInstitute for Vascular Signalling, Centre for Molecular Medicine, Johann Wolfgang Goethe University, 60590 Frankfurt, Germany. fisslthaler@vrc.uni-frankfurt.de.
Goethe University Frankfurt · DE

Funding

Deutsche Forschungsgemeinschaft SFB 834
6 · The paper itself

Abstract

AMP-activated protein kinase (AMPK) is frequently reported to phosphorylate Ser1177 of the endothelial nitric-oxide synthase (eNOS), and therefore, is linked with a relaxing effect. However, previous studies failed to consistently demonstrate a major role for AMPK on eNOS-dependent relaxation. As AMPK also phosphorylates eNOS on the inhibitory Thr495 site, this study aimed to determine the role of AMPKα1 and α2 subunits in the regulation of NO-mediated vascular relaxation. Vascular reactivity to phenylephrine and acetylcholine was assessed in aortic and carotid artery segments from mice with global (AMPKα

Indexed as

AMP-Activated Protein KinasesAnimalsEndothelial CellsHumansMiceMice, KnockoutNitric OxideNitric Oxide Synthase Type IIIPhenylephrinePhosphorylationVasoconstrictionAMP-Activated Protein KinasesNitric OxideNitric Oxide Synthase Type IIIPhenylephrineendothelial cellsendothelial nitric-oxide synthaseionomycinphenylephrinevasoconstrictionvasodilation

Identifiers

PMID30217073
PMCPMC6165563
OpenAlexW2890431136

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.