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Antidotal potency of the novel, structurally different adsorbents in rats acutely intoxicated with the T-2 toxin

dc.contributor.authorJacevic, Vesna Milovan
dc.contributor.authorDumanović, J.
dc.contributor.authorLazarević, M.
dc.contributor.authorNepovimová, Eugenie
dc.contributor.authorResanović, R.
dc.contributor.authorMilovanović, Z.
dc.contributor.authorWu, Qinghua
dc.contributor.authorKuča, Kamil
dc.date.accessioned2026-07-21T06:05:46Z
dc.date.available2026-07-21T06:05:46Z
dc.date.issued2020
dc.description.abstractIn 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 LD50) 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. © 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/).eng
dc.formatp. &quot;Article number 643&quot;
dc.identifier.doi10.3390/toxins12100643
dc.identifier.issn2072-6651
dc.identifier.obd43876766
dc.identifier.scopus2-s2.0-85092287956
dc.identifier.urihttp://hdl.handle.net/20.500.12603/2703
dc.identifier.wos000585352000001
dc.language.isoeng
dc.peerreviewedyes
dc.publicationstatuspostprint
dc.publisherMDPI-Molecular diversity preservation international
dc.relation.ispartofToxins, volume 12, issue: 10eng
dc.relation.publisherversionhttps://www.mdpi.com/2072-6651/12/10/643
dc.rights.accessOpen Access
dc.rights.licenseCC BY
dc.source.urlhttps://www.mdpi.com/2072-6651/12/10/643
dc.subjectAdsorbentseng
dc.subjectAntidoteeng
dc.subjectRatseng
dc.subjectT-2 toxineng
dc.titleAntidotal potency of the novel, structurally different adsorbents in rats acutely intoxicated with the T-2 toxineng
dc.typearticle

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