Evidence map›Paper›PMID 28379159›Full record

ArticleInternational journal of molecular sciences2017

Delphinidin Reduces Glucose Uptake in Mice Jejunal Tissue and Human Intestinal Cells Lines through FFA1/GPR40.

Jorge Hidalgo, Stefanie Teuber, Francisco J Morera, Camila Ojeda, Carlos A Flores, María A Hidalgo, Lucía Núñez, Carlos Villalobos, Rafael A Burgos

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 47 citations in OpenAlex.

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  14. Glucose transporters in the small intestine in health and disease.Pflugers Archiv : European journal of physiology · 2020
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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

9 authors at 3 institutions in 2 countries.

Jorge HidalgoInstitute of Pharmacology and Morphophysiology, Universidad Austral de Chile, 5110566 Valdivia, Chile. jihidalgo.godoy@gmail.com.
Stefanie TeuberInstitute of Pharmacology and Morphophysiology, Universidad Austral de Chile, 5110566 Valdivia, Chile. steubervolke@gmail.com.
Francisco J MoreraInstitute of Pharmacology and Morphophysiology, Universidad Austral de Chile, 5110566 Valdivia, Chile. fjmorera@gmail.com.
Camila OjedaInstitute of Pharmacology and Morphophysiology, Universidad Austral de Chile, 5110566 Valdivia, Chile. camila.ojeda.barria@gmail.com.
Carlos A FloresCentro de Estudios Científicos (CECs), Avenida Arturo Prat 514, 511046 Valdivia, Chile. cflores@cecs.cl.
María A HidalgoInstitute of Pharmacology and Morphophysiology, Universidad Austral de Chile, 5110566 Valdivia, Chile. mahidalgo@uach.cl.
Lucía NúñezInstituto de Biología y Genética Molecular (IBGM), Consejo Superior de Investigaciones Científicas (CSIC), 47003 Valladolid, Spain. nunezl@ibgm.uva.es.
Carlos VillalobosInstituto de Biología y Genética Molecular (IBGM), Consejo Superior de Investigaciones Científicas (CSIC), 47003 Valladolid, Spain. carlosv@ibgm.uva.es.
Rafael A BurgosInstitute of Pharmacology and Morphophysiology, Universidad Austral de Chile, 5110566 Valdivia, Chile. rburgos1@uach.cl.
Austral University of Chile · CLUniversidad de Valladolid · ESCentro de Estudios Científicos · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anthocyanins are pigments with antihyperglycemic properties, and they are potential candidates for developing functional foods for the therapy or prevention of Diabetes mellitus type 2 (DM2). The mechanism of these beneficial effects of anthocyanins are, however, hard to explain, given their very low bioavailability due to poor intestinal absorption. We propose that free fatty acid receptor 1 (FFA1, also named GPR40), is involved in an inhibitory effect of the anthocyanidin delphinidin over intestinal glucose absorption. We show the direct effects of delphinidin on the intestine using jejunum samples from RF/J mice, and the human intestinal cell lines HT-29, Caco-2, and NCM460. By the use of specific pharmacological antagonists, we determined that delphinidin inhibits glucose absorption in both mouse jejunum and a human enterocytic cell line in a FFA1-dependent manner. Delphinidin also affects the function of sodium-glucose cotransporter 1 (SGLT1). Intracellular signaling after FFA1 activation involved cAMP increase and cytosolic Ca

Indexed as

AnimalsAnthocyaninsCaco-2 CellsCalciumCell LineGene Expression RegulationGlucoseHT29 CellsHumansIntestinesJejunumMiceReceptors, G-Protein-CoupledSignal TransductionAnthocyaninsCalciumdelphinidinGlucoseReceptors, G-Protein-CoupledanthocyaninsdelphinidinFFA1glucoseGPR40SGLT1

Identifiers

PMID28379159
PMCPMC5412335
OpenAlexW2605355642

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.