Evidence map›Paper›PMID 22997060›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2013

Comparison of emetic potencies of the 8-ketotrichothecenes deoxynivalenol, 15-acetyldeoxynivalenol, 3-acetyldeoxynivalenol, fusarenon X, and nivalenol.

Wenda Wu, Melissa A Bates, Steven J Bursian, Jane E Link, Brenna M Flannery, Yoshiko Sugita-Konishi, Maiko Watanabe, Haibin Zhang, James J Pestka

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  11. Review
  12. Calcium-Sensing Receptor and Transient Receptor Ankyrin-1 Mediate Emesis Induction by Deoxynivalenol (Vomitoxin).Toxicological sciences : an official journal of the Society of Toxicology · 2017
    Article
  13. Modeling the emetic potencies of food-borne trichothecenes by benchmark dose methodology.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2016
    Article
  14. Article
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  18. Peptide YY3-36 and 5-hydroxytryptamine mediate emesis induction by trichothecene deoxynivalenol (vomitoxin).Toxicological sciences : an official journal of the Society of Toxicology · 2013
    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

9 authors at 3 institutions in 3 countries.

Wenda WuDepartment of Preventive Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, PR China.
Melissa A Bates
Steven J Bursian
Jane E Link
Brenna M Flannery
Yoshiko Sugita-Konishi
Maiko Watanabe
Haibin Zhang
James J Pestka
Michigan State University · USNanjing Agricultural University · CNNational Institute of Health Sciences · JP

Funding

NIEHS NIH HHS ES03553
6 · The paper itself

Abstract

Although the acute toxic effects of trichothecene mycotoxin deoxynivalenol (DON or vomitoxin), a known cause of human food poisoning, have been well characterized in several animal species, much less is known about closely related 8-ketotrichothecenes that similarly occur in cereal grains colonized by toxigenic fusaria. To address this, we compared potencies of DON, 15-acetyldeoxynivalenol (15-ADON), 3-acetyldeoxynivalenol (3-ADON), fusarenon X (FX), and nivalenol (NIV) in the mink emesis model following intraperitoneal (ip) and oral administration. All five congeners dose-dependently induced emesis by both administration methods. With increasing doses, there were marked decreases in latency to emesis with corresponding increases in emesis duration and number of emetic events. The effective doses resulting in emetic events in 50% of the animals for ip exposure to DON, 15-ADON, 3-ADON, FX, and NIV were 80, 170, 180, 70, and 60 µg/kg bw, respectively, and for oral exposure, they were 30, 40, 290, 30, and 250 µg/kg bw, respectively. The emetic potency of DON determined here was comparable to that reported in analogous studies conducted in pigs and dogs, suggesting that the mink is a suitable small animal model for investigating acute trichothecene toxicity. The use of a mouse pica model, based on the consumption of kaolin, was also evaluated as a possible surrogate for studying emesis but was found unsuitable. From a public health perspective, comparative emetic potency data derived from small animal models such as the mink should be useful for establishing toxic equivalency factors for DON and other trichothecenes.

Indexed as

Administration, OralAnimalsDose-Response Relationship, DrugFemaleInjections, IntraperitonealMaleMiceMinkMycotoxinsPicaToxicity TestsTrichothecenesVomiting15-acetyldeoxynivalenol3-acetyldeoxynivalenoldeoxynivalenolfusarenon-XMycotoxinsnivalenolTrichothecenes

Identifiers

PMID22997060
PMCPMC3537132
OpenAlexW2006442892

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.