Evidence map›Paper›PMID 29417944›Full record

ArticleActa pharmacologica Sinica2018

Epicatechin potentiation of glucose-stimulated insulin secretion in INS-1 cells is not dependent on its antioxidant activity.

Kaiyuan Yang, Catherine B Chan

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  4. Antidiabetic Effects and Mechanisms of Action of Uncaria gambir Roxb. in Diabetic Sprague-Dawley Rats.Journal of the American Association for Laboratory Animal Science : JAALAS · 2025
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  7. Review
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  11. Effect ofJournal of diabetes and metabolic disorders · 2021
    Article
  12. Review
  13. Review
  14. Review
  15. Evaluation ofAntioxidants (Basel, Switzerland) · 2020
    Article
  16. Article
  17. A Newly Discovered Phenylethanoid Glycoside fromMolecules (Basel, Switzerland) · 2019
    Article
  18. 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

2 authors at 1 institution in 1 country.

Kaiyuan YangDepartment of Agricultural, Food and Nutritional Science, University of Alberta Edmonton, Alberta, T6G 2E1 Canada.
Catherine B ChanDepartment of Agricultural, Food and Nutritional Science, University of Alberta Edmonton, Alberta, T6G 2E1 Canada.
University of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epicatechin (EC) is a monomeric flavan-3-ol. We have previously demonstrated that glucose-intolerant rats fed flavan-3-ols exhibit improved pancreatic islet function corresponding with an increase in circulating EC-derived metabolites. Thus, we speculate that EC may act as a cellular signaling molecule in vivo to modulate insulin secretion. In this study we further examined the effects of different concentrations of EC on H2O2 or hyperglycemia-induced ROS production, as well as on saturated fatty acid (SFA)-impaired glucose-stimulated insulin secretion (GSIS) in INS-1 cell line in vitro. We showed that EC at a high concentration (30 μmol/L), but not a low concentration (0.3 μmol/L), significantly decreased H2O2 or hyperglycemia-induced ROS production in INS-1 cells. However, EC (0.3 μmol/L) significantly enhanced SFA-impaired GSIS in INS-1 cells. Addition of KN-93, a CaMKII inhibitor, blocked the effect of EC on insulin secretion and decreased CaMKII phosphorylation. Addition of GW1100, a GPR40 antagonist, significantly attenuated EC-enhanced GSIS, but only marginally affected CaMKII phosphorylation. These results demonstrate that EC at a physiological concentration promotes GSIS in SFA-impaired β-cells via activation of the CaMKII pathway and is consistent with its function as a GPR40 ligand. The findings support a role for EC as a cellular signaling molecule in vivo and further delineate the signaling pathways of EC in β-cells.

Indexed as

AnimalsBenzenesulfonamidesBenzoatesBenzylaminesCalcium-Calmodulin-Dependent Protein Kinase Type 2CatechinCell LineDose-Response Relationship, DrugFatty AcidsGlucoseHydrogen PeroxideInsulinInsulin-Secreting CellsInsulin SecretionLigandsPyrimidinesBenzenesulfonamidesBenzoatesBenzylaminesCalcium-Calmodulin-Dependent Protein Kinase Type 2CatechinFatty AcidsGlucoseG-protein-coupled receptor 40, ratGW1100Hydrogen PeroxideInsulinKN 93LigandsPyrimidinesReceptors, G-Protein-CoupledSulfonamides

Identifiers

PMID29417944
PMCPMC5943899
OpenAlexW2785805078

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.