Evidence map›Paper›PMID 26517901›Full record

ReviewBiochemical Society transactions2015

Molecular action of sulphonylureas on KATP channels: a real partnership between drugs and nucleotides.

Heidi de Wet, Peter Proks

Erratum issuedAbstract readReview
In one paragraph

Review in Biochemical Society transactions, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
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  10. Review
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  15. Review
  16. Article
  17. Development of IFrontiers in pharmacology · 2021
    Article
  18. Article
  19. Article
  20. Role of Caveolin-1 in Diabetes and Its Complications.Oxidative medicine and cellular longevity · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Heidi de WetDepartment of Physiology, Anatomy and Genetics, Le Gros Clark building, University of Oxford, South Parks Road, Oxford OX1 3QX, England, U.K.
Peter ProksDepartment of Physiology, Anatomy and Genetics, Le Gros Clark building, University of Oxford, South Parks Road, Oxford OX1 3QX, England, U.K. peter.proks@dpag.ox.ac.uk.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Sulphonylureas stimulate insulin secretion from pancreatic β-cells primarily by closing ATP-sensitive K(+) channels in the β-cell plasma membrane. The mechanism of channel inhibition by these drugs is unusually complex. As direct inhibitors of channel activity, sulphonylureas act only as partial antagonists at therapeutic concentrations. However, they also exert an additional indirect inhibitory effect via modulation of nucleotide-dependent channel gating. In this review, we summarize current knowledge and recent advances in our understanding of the molecular mechanism of action of these drugs.

Indexed as

Adenosine TriphosphateDiabetes MellitusHumansInfant, NewbornInsulinInsulin SecretionIon Channel GatingIslets of LangerhansKATP ChannelsMembrane PotentialsSulfonylurea CompoundsAdenosine TriphosphateInsulinKATP ChannelsSulfonylurea CompoundsABCC8diabetesKATP channelsKir6.2SUR1

Identifiers

PMID26517901
PMCPMC4613533

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.