Evidence map›Paper›PMID 24533087›Full record

ArticlePloS one2014

Characterization of a novel glucokinase activator in rat and mouse models.

Min Lu, Pingping Li, Gautam Bandyopadhyay, William Lagakos, Walter E Dewolf, Taylor Alford, Mark Joseph Chicarelli, Lance Williams, Deborah A Anderson, Brian R Baer and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Review
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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

14 authors at 3 institutions in 1 country.

Min LuDepartment of Medicine, University of California San Diego, La Jolla, California, United States of America.
Pingping LiDepartment of Medicine, University of California San Diego, La Jolla, California, United States of America.
Gautam BandyopadhyayDepartment of Medicine, University of California San Diego, La Jolla, California, United States of America.
William LagakosDepartment of Medicine, University of California San Diego, La Jolla, California, United States of America.
Walter E DewolfArray BioPharma Inc., Boulder, Colorado, United States of America.
Taylor AlfordArray BioPharma Inc., Boulder, Colorado, United States of America.
Mark Joseph ChicarelliArray BioPharma Inc., Boulder, Colorado, United States of America.
Lance WilliamsArray BioPharma Inc., Boulder, Colorado, United States of America.
Deborah A AndersonArray BioPharma Inc., Boulder, Colorado, United States of America.
Brian R BaerArray BioPharma Inc., Boulder, Colorado, United States of America.
Maralee McVeanArray BioPharma Inc., Boulder, Colorado, United States of America.
Marion ConnAmgen Inc., South San Francisco, California, United States of America.
Murielle M VéniantAmgen Inc., Thousand Oaks, California, United States of America.
Peter CowardAmgen Inc., South San Francisco, California, United States of America.
Array BioPharma (United States) · USUniversity of California, San Diego · USAmgen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucokinase (GK) is a hexokinase isozyme that catalyzes the phosphorylation of glucose to glucose-6-phosphate. Glucokinase activators are being investigated as potential diabetes therapies because of their effects on hepatic glucose output and/or insulin secretion. Here, we have examined the efficacy and mechanisms of action of a novel glucokinase activator, GKA23. In vitro, GKA23 increased the affinity of rat and mouse glucokinase for glucose, and increased glucose uptake in primary rat hepatocytes. In vivo, GKA23 treatment improved glucose homeostasis in rats by enhancing beta cell insulin secretion and suppressing hepatic glucose production. Sub-chronic GKA23 treatment of mice fed a high-fat diet resulted in improved glucose homeostasis and lipid profile.

Indexed as

AminopyridinesAnimalsArea Under CurveBlood GlucoseCatalysisDiabetes Mellitus, ExperimentalEnzyme ActivatorsGlucokinaseGlucoseGlucose Tolerance TestHepatocytesHomeostasisInsulinInsulin-Secreting CellsInsulin SecretionKinetics1-(5-(3-(2,6-dimethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)ethane-1,2-diolAminopyridinesBlood GlucoseEnzyme ActivatorsGlucokinaseGlucoseInsulinThiadiazoles

Identifiers

PMID24533087
PMCPMC3922816
OpenAlexW2033218216

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.