Evidence map›Paper›PMID 27618100›Full record

ArticleToxins2016

Early Activation of MAPK p44/42 Is Partially Involved in DON-Induced Disruption of the Intestinal Barrier Function and Tight Junction Network.

Alexandra Springler, Sabine Hessenberger, Gerd Schatzmayr, Elisabeth Mayer

Open access · goldAbstract readComparative Study
In one paragraph

Article in Toxins, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
14.4field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 49 citations in OpenAlex.

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  8. Traditional and emergingAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2023
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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

4 authors.

Alexandra SpringlerBiomin Research Center, Technopark 1, 3430 Tulln an der Donau, Austria. alexandra.springler@biomin.net.
Sabine HessenbergerBiomin Research Center, Technopark 1, 3430 Tulln an der Donau, Austria. sabine.hessenberger@biomin.net.
Gerd SchatzmayrBiomin Research Center, Technopark 1, 3430 Tulln an der Donau, Austria. gerd.schatzmayr@biomin.net.
Elisabeth MayerBiomin Research Center, Technopark 1, 3430 Tulln an der Donau, Austria. e.mayer@biomin.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deoxynivalenol (DON), produced by the plant pathogens Fusarium graminearum and Fusarium culmorum, is one of the most common mycotoxins, contaminating cereal and cereal-derived products. Although worldwide contamination of food and feed poses health threats to humans and animals, pigs are particularly susceptible to this mycotoxin. DON derivatives, such as deepoxy-deoxynivalenol (DOM-1), are produced by bacterial transformation of certain intestinal bacteria, which are naturally occurring or applied as feed additives. Intestinal epithelial cells are the initial barrier against these food- and feed-borne toxins. The present study confirms DON-induced activation of MAPK p44/42 and inhibition of p44/42 by MAPK-inhibitor U0126 monoethanolate. Influence of DON and DOM-1 on transepithelial electrical resistance (TEER), viability and expression of seven tight junction proteins (TJ), as well as the potential of U0126 to counteract DON-induced effects, was assessed. While DOM-1 showed no effect, DON significantly reduced TEER of differentiated IPEC-J2 and decreased expression of claudin-1 and -3, while leaving claudin-4; ZO-1, -2, and -3 and occludin unaffected. Inhibition of p44/42 counteracted DON-induced TEER decrease and restored claudin-3, but not claudin-1 expression. Therefore, effects of DON on TEER and claudin-3 are at least partially p44/42 mediated, while effects on viability and claudin-1 are likely mediated via alternative pathways.

Indexed as

AnimalsCalcium SignalingCell LineCell SurvivalDose-Response Relationship, DrugElectric ImpedanceEnzyme ActivationEpithelial CellsIntestinal MucosaMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3PermeabilityProtein Kinase InhibitorsSwineTight Junction ProteinsTight Junctionsdeepoxy-deoxynivalenoldeoxynivalenolMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Protein Kinase InhibitorsTight Junction ProteinsTrichothecenesde-epoxy deoxynivalenoldeoxynivalenolIPEC-J2mycotoxintight junctionstransepithelial electrical resistance

Identifiers

PMID27618100
PMCPMC5037490
OpenAlexW2513105124

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.