Evidence map›Paper›PMID 17947353›Full record

ArticleEndocrinology2008

Dexamethasone sensitizes the neonatal intestine to fructose induction of intestinal fructose transporter (Slc2A5) function.

Veronique Douard, Xue-Lin Cui, Patricia Soteropoulos, Ronaldo P Ferraris

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. GLUT5: structure, functions, diseases and potential applications.Acta biochimica et biophysica Sinica · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Intestinal Absorption of Fructose.Annual review of nutrition · 2018
    Review
  10. Glucose transporter expression in the human colon.World journal of gastroenterology · 2018
    Article
  11. Article
  12. Article
  13. Transport, metabolism, and endosomal trafficking-dependent regulation of intestinal fructose absorption.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  14. Article
  15. Article
  16. Review
  17. Dietary fructose inhibits lactation-induced adaptations in rat 1,25-(OH)₂D₃ synthesis and calcium transport.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Veronique DouardDepartment of Pharmacology and Physiology, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark, New Jersey 07101-1709, USA.
Xue-Lin Cui
Patricia Soteropoulos
Ronaldo P Ferraris
Rutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · US

Funding

Regulation of intestinal phosphate uptake by dietary carbohydrateR21DK075617 · NIDDK · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI FERRARIS, RONALDO PARAOAN · 2007 to 2008
$424k
NIDDK NIH HHS R21 DK075617PHS HHS RDK075617A
6 · The paper itself

Abstract

The recent dramatic increase in fructose consumption is tightly correlated with an equally dramatic surge in the incidence of type 2 diabetes and obesity in children, but little is known about dietary fructose metabolism and absorption in neonates. The expression of the rat intestinal fructose transporter GLUT5 [Slc2A5, a member of the glucose transporter family (GLUT)] can be specifically induced by its substrate fructose, but only after weaning begins at 14 d of age. In suckling rats younger than 14 d old, dietary fructose cannot enhance GLUT5 expression. The aim of this study was to identify the mechanisms allowing fructose to stimulate GLUT5 during weaning. After intestines were perfused with fructose or glucose (control), using microarray hybridization we showed that of 5K genes analyzed in 10-d-old pups, only 13 were fructose responsive. Previous work found approximately 50 fructose-responsive genes in 20-d-old pups. To identify fructose-responsive genes whose expression also changed with age, intestines of 10- and 20-d-old littermate pups perfused with fructose were compared by microarray. Intestines of 10- and 20-d-old pups perfused with glucose were used to segregate age- but not fructose-responsive genes. About 28 genes were up- and 22 down-regulated in 20- relative to 10-d-old pups, under conditions of fructose perfusion, and many were found, by cluster analysis, to be regulated by corticosterone. When dexamethasone was injected into suckling pups before fructose perfusion, the expression of GLUT5 but not that of the sodium glucose cotransporter (SGLT) 1 and of GLUT2, as well as the uptake of fructose but not of glucose increased dramatically. Thus, dexamethasone, which allows dietary fructose to precociously stimulate intestinal fructose absorption, can mimic the effect of age and modify developmental timing mechanisms regulating GLUT5.

Indexed as

Age FactorsAnimalsAnimals, NewbornAnimals, SucklingDexamethasoneDrug SynergismFructoseGene Expression ProfilingGene Expression RegulationGlucoseGlucose Transporter Type 5Intestinal MucosaIntestinesModels, BiologicalOligonucleotide Array Sequence AnalysisRatsDexamethasoneFructoseGlucoseGlucose Transporter Type 5Slc2a5 protein, rat

Identifiers

PMID17947353
PMCPMC2194616
OpenAlexW1964995085

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.