Cargando…

Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol

Trichothecene mycotoxins are common contaminants in cereal grains and negatively impact human and animal health. Although anorexia is a common hallmark of type B trichothecenes-induced toxicity, less is known about the anorectic potencies of type A trichothecenes. The purpose of this study was to co...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Jie, Zhang, Hua, Liu, Shengli, Wu, Wenda, Zhang, Haibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5983235/
https://www.ncbi.nlm.nih.gov/pubmed/29710820
http://dx.doi.org/10.3390/toxins10050179
_version_ 1783328388632543232
author Zhang, Jie
Zhang, Hua
Liu, Shengli
Wu, Wenda
Zhang, Haibin
author_facet Zhang, Jie
Zhang, Hua
Liu, Shengli
Wu, Wenda
Zhang, Haibin
author_sort Zhang, Jie
collection PubMed
description Trichothecene mycotoxins are common contaminants in cereal grains and negatively impact human and animal health. Although anorexia is a common hallmark of type B trichothecenes-induced toxicity, less is known about the anorectic potencies of type A trichothecenes. The purpose of this study was to compare the anorectic potencies of four type A trichothecenes (T-2 toxin (T-2), HT-2 toxin (HT-2), diacetoxyscirpenol (DAS), and neosolaniol (NEO)) in mice. Following oral exposure to T-2, HT-2, DAS, and NEO, the no observed adverse effect levels (NOAELs) and lowest observed adverse effect levels (LOAELs) were 0.01, 0.01, 0.1, and 0.01 mg/kg body weight (BW), and 0.1, 0.1, 0.5, and 0.1 mg/kg BW, respectively. Following intraperitoneal (IP) exposure to T-2, HT-2, DAS, and NEO, the NOAELs were 0.01 mg/kg BW, except for DAS (less than 0.01 mg/kg BW), and the LOAELs were 0.1, 0.1, 0.01, and 0.1 mg/kg BW, respectively. Taken together, the results suggest that (1) type A trichothecenes could dose-dependently elicit anorectic responses following both oral gavage and IP exposure in mice; (2) the anorectic responses follow an approximate rank order of T-2 = HT-2 = NEO > DAS for oral exposure, and DAS > T-2 = HT-2 = NEO for IP administration; (3) IP exposure to T-2, HT-2, DAS, and NEO evoked stronger anorectic effects than oral exposure. From a public health perspective, comparative anorectic potency data should be useful for establishing toxic equivalency factors for type A trichothecenes.
format Online
Article
Text
id pubmed-5983235
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-59832352018-06-06 Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol Zhang, Jie Zhang, Hua Liu, Shengli Wu, Wenda Zhang, Haibin Toxins (Basel) Article Trichothecene mycotoxins are common contaminants in cereal grains and negatively impact human and animal health. Although anorexia is a common hallmark of type B trichothecenes-induced toxicity, less is known about the anorectic potencies of type A trichothecenes. The purpose of this study was to compare the anorectic potencies of four type A trichothecenes (T-2 toxin (T-2), HT-2 toxin (HT-2), diacetoxyscirpenol (DAS), and neosolaniol (NEO)) in mice. Following oral exposure to T-2, HT-2, DAS, and NEO, the no observed adverse effect levels (NOAELs) and lowest observed adverse effect levels (LOAELs) were 0.01, 0.01, 0.1, and 0.01 mg/kg body weight (BW), and 0.1, 0.1, 0.5, and 0.1 mg/kg BW, respectively. Following intraperitoneal (IP) exposure to T-2, HT-2, DAS, and NEO, the NOAELs were 0.01 mg/kg BW, except for DAS (less than 0.01 mg/kg BW), and the LOAELs were 0.1, 0.1, 0.01, and 0.1 mg/kg BW, respectively. Taken together, the results suggest that (1) type A trichothecenes could dose-dependently elicit anorectic responses following both oral gavage and IP exposure in mice; (2) the anorectic responses follow an approximate rank order of T-2 = HT-2 = NEO > DAS for oral exposure, and DAS > T-2 = HT-2 = NEO for IP administration; (3) IP exposure to T-2, HT-2, DAS, and NEO evoked stronger anorectic effects than oral exposure. From a public health perspective, comparative anorectic potency data should be useful for establishing toxic equivalency factors for type A trichothecenes. MDPI 2018-04-29 /pmc/articles/PMC5983235/ /pubmed/29710820 http://dx.doi.org/10.3390/toxins10050179 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Jie
Zhang, Hua
Liu, Shengli
Wu, Wenda
Zhang, Haibin
Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol
title Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol
title_full Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol
title_fullStr Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol
title_full_unstemmed Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol
title_short Comparison of Anorectic Potencies of Type A Trichothecenes T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol
title_sort comparison of anorectic potencies of type a trichothecenes t-2 toxin, ht-2 toxin, diacetoxyscirpenol, and neosolaniol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5983235/
https://www.ncbi.nlm.nih.gov/pubmed/29710820
http://dx.doi.org/10.3390/toxins10050179
work_keys_str_mv AT zhangjie comparisonofanorecticpotenciesoftypeatrichothecenest2toxinht2toxindiacetoxyscirpenolandneosolaniol
AT zhanghua comparisonofanorecticpotenciesoftypeatrichothecenest2toxinht2toxindiacetoxyscirpenolandneosolaniol
AT liushengli comparisonofanorecticpotenciesoftypeatrichothecenest2toxinht2toxindiacetoxyscirpenolandneosolaniol
AT wuwenda comparisonofanorecticpotenciesoftypeatrichothecenest2toxinht2toxindiacetoxyscirpenolandneosolaniol
AT zhanghaibin comparisonofanorecticpotenciesoftypeatrichothecenest2toxinht2toxindiacetoxyscirpenolandneosolaniol