Evidence map›Paper›PMID 29414682›Full record

ArticleCell metabolism2018

The HETE Is on FFAR1 and Pancreatic Islet Cells.

Mette Trauelsen, Michael Lückmann, Thomas M Frimurer, Thue W Schwartz

Open access · bronzeAbstract readComment
PubMed Publisher
In one paragraph

Article in Cell metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Metabolic and Molecular Amplification of Insulin Secretion.Advances in anatomy, embryology, and cell biology · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Molecular dynamics-guided discovery of an ago-allosteric modulator for GPR40/FFAR1.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Mette TrauelsenCenter for Basic Metabolic Research, University of Copenhagen, Denmark.
Michael LückmannCenter for Basic Metabolic Research, University of Copenhagen, Denmark.
Thomas M FrimurerCenter for Basic Metabolic Research, University of Copenhagen, Denmark.
Thue W SchwartzCenter for Basic Metabolic Research, University of Copenhagen, Denmark; Laboratory for Molecular Pharmacology, Department for Biomedical Research, Faculty of Health Sciences, University of Copenhagen, Denmark. Electronic address: tws@sund.ku.dk.
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is known but generally unappreciated that the fatty acid receptor FFAR1 (GPR40) is responsible for a major part of glucose-induced insulin secretion. This puzzling fact is now explained by Tunaru et al. (2018), who demonstrate that glucose-induced 20-hydroxyeicosatetraenoic acid (20-HETE) amplifies insulin secretion through autocrine activation of FFAR1.

Indexed as

GlucoseInsulinHydroxyeicosatetraenoic AcidsInsulin SecretionIslets of LangerhansReceptors, G-Protein-Coupled20-hydroxy-5,8,11,14-eicosatetraenoic acidGlucoseHydroxyeicosatetraenoic AcidsInsulinReceptors, G-Protein-Coupled

Identifiers

PMID29414682
OpenAlexW2785550743

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.