Evidence map›Paper›PMID 28821741›Full record

ArticleScientific reports2017

Predicting the murine enterocyte metabolic response to diets that differ in lipid and carbohydrate composition.

Neeraj Sinha, Maria Suarez-Diez, Evert M van Schothorst, Jaap Keijer, Vitor A P Martins Dos Santos, Guido J E J Hooiveld

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
0.6field-weighted citation impact, top 30% 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, 11 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Neeraj SinhaNutrition, Metabolism & Genomics Group, Division of Human Nutrition, Wageningen University, Stippeneng 4, Wageningen, 6708 WE, The Netherlands.
Maria Suarez-DiezLaboratory of Systems and Synthetic Biology, Wageningen University, Stippeneng 4, Wageningen, 6708 WE, The Netherlands.ORCID 0000-0001-5845-146X
Evert M van SchothorstHuman and Animal Physiology, Wageningen University, De Elst 1, Wageningen, 6708 WD, The Netherlands.ORCID 0000-0002-3036-5903
Jaap KeijerHuman and Animal Physiology, Wageningen University, De Elst 1, Wageningen, 6708 WD, The Netherlands.
Vitor A P Martins Dos SantosLaboratory of Systems and Synthetic Biology, Wageningen University, Stippeneng 4, Wageningen, 6708 WE, The Netherlands.
Guido J E J HooiveldNutrition, Metabolism & Genomics Group, Division of Human Nutrition, Wageningen University, Stippeneng 4, Wageningen, 6708 WE, The Netherlands. guido.hooiveld@wur.nl.ORCID 0000-0003-1954-3542
Wageningen University & Research · NLLifeGlimmer (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The small intestine serves as gatekeeper at the interface between body and diet and is thought to play an important role in the etiology of obesity and associated metabolic disorders. A computational modelling approach was used to improve our understanding of the metabolic responses of epithelial cells to different diets. A constraint based, mouse-specific enterocyte metabolic model (named mmu_ENT717) was constructed to describe the impact of four fully characterized semi-purified diets, that differed in lipid and carbohydrate composition, on uptake, metabolism, as well as secretion of carbohydrates and lipids. Our simulation results predicted luminal sodium as a limiting factor for active glucose absorption; necessity of apical localization of glucose transporter GLUT2 for absorption of all glucose in the postprandial state; potential for gluconeogenesis in enterocytes; and the requirement of oxygen for the formation of endogenous cholesterol needed for chylomicron formation under luminal cholesterol-free conditions. In addition, for a number of enzymopathies related to intestinal carbohydrate and lipid metabolism it was found that their effects might be ameliorated through dietary interventions. In conclusion, our improved enterocyte-specific model was shown to be a suitable platform to study effects of dietary interventions on enterocyte metabolism, and provided novel and deeper insights into enterocyte metabolism.

Indexed as

Carbohydrate MetabolismLipid MetabolismAnimalsDietDietary CarbohydratesEnterocytesGlucoseHumansMetabolic Networks and PathwaysMiceDietary CarbohydratesGlucose

Identifiers

PMID28821741
PMCPMC5562867
OpenAlexW2747841644

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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.