Evidence map›Paper›PMID 26295259›Full record

ArticleToxins2015

Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins.

Łukasz Zielonka, Agnieszka Waśkiewicz, Monika Beszterda, Marian Kostecki, Michał Dąbrowski, Kazimierz Obremski, Piotr Goliński, Maciej Gajęcki

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.2field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

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  10. Current research in toxicology · 2021
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  12. Animal nutrition (Zhongguo xu mu shou yi xue hui) · 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

8 authors at 2 institutions in 1 country.

Łukasz ZielonkaDepartment of Veterinary Prevention and Feed Hygiene, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Olsztyn 10-719, Poland. lukasz.zielonka@uwm.ed.pl.
Agnieszka WaśkiewiczDepartment of Chemistry, Poznań University of Life Sciences, Wojska Polskiego 75, Poznań 60-625, Poland. agat@up.poznan.pl.
Monika BeszterdaDepartment of Chemistry, Poznań University of Life Sciences, Wojska Polskiego 75, Poznań 60-625, Poland. monika.beszterda@up.poznan.pl.
Marian KosteckiDepartment of Chemistry, Poznań University of Life Sciences, Wojska Polskiego 75, Poznań 60-625, Poland. marian.kostecki@up.poznan.pl.
Michał DąbrowskiDepartment of Veterinary Prevention and Feed Hygiene, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Olsztyn 10-719, Poland. michal.dabrowski@uwm.edu.pl.
Kazimierz ObremskiDepartment of Veterinary Prevention and Feed Hygiene, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Olsztyn 10-719, Poland. obremski@uwm.edu.pl.
Piotr GolińskiDepartment of Chemistry, Poznań University of Life Sciences, Wojska Polskiego 75, Poznań 60-625, Poland. piotrg@up.poznan.pl.
Maciej GajęckiDepartment of Veterinary Prevention and Feed Hygiene, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Olsztyn 10-719, Poland. gajecki@uwm.edu.pl.
University of Life Sciences in Poznań · PLUniversity of Warmia and Mazury in Olsztyn · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zearalenone and its metabolites, α-zearalenol and β-zearalenol, demonstrate estradiol-like activity and disrupt physiological functions in animals. This article evaluates the carryover of zearalenone and its selected metabolites from the digesta to intestinal walls (along the entire intestines) in pre-pubertal gilts exposed to low doses of zearalenone over long periods of time. The term "carryover" describes the transfer of mycotoxins from feed to edible tissues, and it was used to assess the risk of mycotoxin exposure for consumers. The experimental gilts with body weight of up to 25 kg were per os administered zearalenone at a daily dose of 40 μg/kg BW (Group E, n = 18) or placebo (Group C, n = 21) over a period of 42 days. In the first weeks of exposure, the highest values of the carryover factor were noted in the duodenum and the jejunum. In animals receiving pure zearalenone, the presence of metabolites was not determined in intestinal tissues. In the last three weeks of the experiment, very high values of the carryover factor were observed in the duodenum and the descending colon. The results of the study indicate that in animals exposed to subclinical doses of zearalenone, the carryover factor could be determined by the distribution and expression of estrogen receptor beta.

Indexed as

AnimalsFemaleIntestinal MucosaLiverSwineZearalenoneZearalenonecarryovergiltsintestinemetabolitesper oszearalenone

Identifiers

PMID26295259
PMCPMC4549746
OpenAlexW1636750947

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.