Evidence map›Paper›PMID 41821547›Full record

ArticleFood science of animal resources2025

Growth Characteristics, Blood Biochemistry, Histology, and Metabolic Profile of Muscle and Different Tissues: Toxicity Study of Deoxynivalenol.

Jin Young Jeong, Junsik Kim, Minji Kim, Sungkwon Park

Abstract read
In one paragraph

Article in Food science of animal resources, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jin Young JeongPrecision Animal Nutrition Division, National Institute of Animal Science, Wanju 55365, Korea.ORCID https://orcid.org/0000-0002-8670-7036
Junsik KimPrecision Animal Nutrition Division, National Institute of Animal Science, Wanju 55365, Korea.ORCID https://orcid.org/0000-0001-9692-757X
Minji KimPrecision Animal Nutrition Division, National Institute of Animal Science, Wanju 55365, Korea.ORCID https://orcid.org/0000-0003-2106-1921
Sungkwon ParkDepartment of Food Science and Biotechnology, Sejong University, Seoul 05006, Korea.ORCID https://orcid.org/0000-0002-7684-9719

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deoxynivalenol (DON) toxicity causes oxidative stress, immunological disorders, and gastrointestinal injury, thereby reducing animal survival and productivity. Pigs are particularly susceptible to DON; therefore, clear standards for DON levels in animal feed are essential. Therefore, we investigated the growth characteristics, biochemistry, histology, and metabolite profiles of growing pigs fed dietary DON levels. Twelve pigs were randomized to one of four diets for 28 d: 1) CON, control group fed conventional diets; 2) T1, 1 mg; 3) T2, 3 mg; and 4) T3, 10 mg DON/kg conventional diet. The results revealed that the final body weight of the growing pigs in the T3 group was the lowest among all DON-treated groups (p<0.05). Additionally, the T3 group demonstrated the highest blood alkaline phosphate levels, whereas the T2 and T3 treatment groups exhibited reduced lipase levels compared to the other groups (p<0.01). Histological analysis showed that fibrosis increased in the muscle, liver, and other tissues, while apoptosis increased in the liver and ileum with increasing DON levels. Metabolomic profiling revealed that several metabolic pathways, such as purine metabolism, were involved in the weight loss induced by DON toxicity. In conclusion, our study suggests that DON levels above the maximum residue limits have adverse effects on growing pigs and that these effects are caused by altered metabolites.

Indexed as

deoxynivalenolgrowing pighistologymetabolite

Identifiers

PMID41821547
PMCPMC12965360

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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.