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Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin
In this paper, the potential antidote efficacy of commercially available formulations of various feed additives such as Minazel-Plus(®), Mycosorb(®), and Mycofix(®) was considered by recording their incidence on general health, body weight, and food and water intake, as well as through histopatholog...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600379/ https://www.ncbi.nlm.nih.gov/pubmed/33028026 http://dx.doi.org/10.3390/toxins12100643 |
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author | Jaćević, Vesna Dumanović, Jelena Lazarević, Miodrag Nepovimova, Eugenie Resanović, Radmila Milovanović, Zoran Wu, Qinghua Kuča, Kamil |
author_facet | Jaćević, Vesna Dumanović, Jelena Lazarević, Miodrag Nepovimova, Eugenie Resanović, Radmila Milovanović, Zoran Wu, Qinghua Kuča, Kamil |
author_sort | Jaćević, Vesna |
collection | PubMed |
description | In this paper, the potential antidote efficacy of commercially available formulations of various feed additives such as Minazel-Plus(®), Mycosorb(®), and Mycofix(®) was considered by recording their incidence on general health, body weight, and food and water intake, as well as through histopathology and semiquantitative analysis of gastric alterations in Wistar rats treated with the T-2 toxin in a single-dose regimen of 1.67 mg/kg p.o. (1 LD(50)) for 4 weeks. As an organic adsorbent, Mycosorb(®) successfully antagonized acute lethal incidence of the T-2 toxin (protective index (PI) = 2.25; p < 0.05 vs. T-2 toxin), and had adverse effects on body weight gain as well as food and water intake during the research (p < 0.001). However, the protective efficacy of the other two food additives was significantly lower (p < 0.05). Treatment with Mycosorb(®) significantly reduced the severity of gastric damage, which was not the case when the other two adsorbents were used. Our results suggest that Mycosorb(®) is a much better adsorbent for preventing the adverse impact of the T-2 toxin as well as its toxic metabolites compared with Minazel-plus(®) or Mycofix-plus(®), and it almost completely suppresses its acute toxic effects and cytotoxic potential on the gastric epithelial, glandular, and vascular endothelial cells. |
format | Online Article Text |
id | pubmed-7600379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76003792020-11-01 Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin Jaćević, Vesna Dumanović, Jelena Lazarević, Miodrag Nepovimova, Eugenie Resanović, Radmila Milovanović, Zoran Wu, Qinghua Kuča, Kamil Toxins (Basel) Article In this paper, the potential antidote efficacy of commercially available formulations of various feed additives such as Minazel-Plus(®), Mycosorb(®), and Mycofix(®) was considered by recording their incidence on general health, body weight, and food and water intake, as well as through histopathology and semiquantitative analysis of gastric alterations in Wistar rats treated with the T-2 toxin in a single-dose regimen of 1.67 mg/kg p.o. (1 LD(50)) for 4 weeks. As an organic adsorbent, Mycosorb(®) successfully antagonized acute lethal incidence of the T-2 toxin (protective index (PI) = 2.25; p < 0.05 vs. T-2 toxin), and had adverse effects on body weight gain as well as food and water intake during the research (p < 0.001). However, the protective efficacy of the other two food additives was significantly lower (p < 0.05). Treatment with Mycosorb(®) significantly reduced the severity of gastric damage, which was not the case when the other two adsorbents were used. Our results suggest that Mycosorb(®) is a much better adsorbent for preventing the adverse impact of the T-2 toxin as well as its toxic metabolites compared with Minazel-plus(®) or Mycofix-plus(®), and it almost completely suppresses its acute toxic effects and cytotoxic potential on the gastric epithelial, glandular, and vascular endothelial cells. MDPI 2020-10-05 /pmc/articles/PMC7600379/ /pubmed/33028026 http://dx.doi.org/10.3390/toxins12100643 Text en © 2020 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 Jaćević, Vesna Dumanović, Jelena Lazarević, Miodrag Nepovimova, Eugenie Resanović, Radmila Milovanović, Zoran Wu, Qinghua Kuča, Kamil Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin |
title | Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin |
title_full | Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin |
title_fullStr | Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin |
title_full_unstemmed | Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin |
title_short | Antidotal Potency of the Novel, Structurally Different Adsorbents in Rats Acutely Intoxicated with the T-2 Toxin |
title_sort | antidotal potency of the novel, structurally different adsorbents in rats acutely intoxicated with the t-2 toxin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600379/ https://www.ncbi.nlm.nih.gov/pubmed/33028026 http://dx.doi.org/10.3390/toxins12100643 |
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