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In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1

Mycotoxins are natural food and feed contaminants produced by several molds. The primary mode of exposure in humans and animals is through mixtures. Aflatoxin B1 (AFB1) and sterigmatocystin (STER) are structurally related mycotoxins that share the same biosynthetic route. Few in vivo genotoxicity as...

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Autores principales: Alonso-Jauregui, Maria, López de Cerain, Adela, Azqueta, Amaya, Rodriguez-Garraus, Adriana, Gil, Ana Gloria, González-Peñas, Elena, Vettorazzi, Ariane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467059/
https://www.ncbi.nlm.nih.gov/pubmed/37624248
http://dx.doi.org/10.3390/toxins15080491
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author Alonso-Jauregui, Maria
López de Cerain, Adela
Azqueta, Amaya
Rodriguez-Garraus, Adriana
Gil, Ana Gloria
González-Peñas, Elena
Vettorazzi, Ariane
author_facet Alonso-Jauregui, Maria
López de Cerain, Adela
Azqueta, Amaya
Rodriguez-Garraus, Adriana
Gil, Ana Gloria
González-Peñas, Elena
Vettorazzi, Ariane
author_sort Alonso-Jauregui, Maria
collection PubMed
description Mycotoxins are natural food and feed contaminants produced by several molds. The primary mode of exposure in humans and animals is through mixtures. Aflatoxin B1 (AFB1) and sterigmatocystin (STER) are structurally related mycotoxins that share the same biosynthetic route. Few in vivo genotoxicity assays have been performed with STER. In the present genotoxicity study, Wistar rats were dosed orally with STER (20 mg/kg b.w.), AFB1 (0.25 mg/kg b.w.) or a mixture of both in an integrated micronucleus (bone marrow) and comet study (liver and kidney). STER was dosed at the highest feasible dose in corn oil. No increase in the percentage of micronuclei in bone marrow was observed at any condition. Slight DNA damage was detected in the livers of animals treated with AFB1 or the mixture (DNA strand breaks and Fpg (Formamidopyrimidine DNA glycosylase)-sensitive sites, respectively). Plasma, liver, and kidney samples were analyzed with LC-MS/MS demonstrating exposure to both mycotoxins. General toxicity parameters (organs absolute weight, biochemistry, and histopathology) were not altered either individually or in the mixture. The overall absence of individual genotoxicity did not allow us to set any type of interaction in the mixture. However, a possible toxicokinetic interaction was observed.
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spelling pubmed-104670592023-08-31 In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1 Alonso-Jauregui, Maria López de Cerain, Adela Azqueta, Amaya Rodriguez-Garraus, Adriana Gil, Ana Gloria González-Peñas, Elena Vettorazzi, Ariane Toxins (Basel) Article Mycotoxins are natural food and feed contaminants produced by several molds. The primary mode of exposure in humans and animals is through mixtures. Aflatoxin B1 (AFB1) and sterigmatocystin (STER) are structurally related mycotoxins that share the same biosynthetic route. Few in vivo genotoxicity assays have been performed with STER. In the present genotoxicity study, Wistar rats were dosed orally with STER (20 mg/kg b.w.), AFB1 (0.25 mg/kg b.w.) or a mixture of both in an integrated micronucleus (bone marrow) and comet study (liver and kidney). STER was dosed at the highest feasible dose in corn oil. No increase in the percentage of micronuclei in bone marrow was observed at any condition. Slight DNA damage was detected in the livers of animals treated with AFB1 or the mixture (DNA strand breaks and Fpg (Formamidopyrimidine DNA glycosylase)-sensitive sites, respectively). Plasma, liver, and kidney samples were analyzed with LC-MS/MS demonstrating exposure to both mycotoxins. General toxicity parameters (organs absolute weight, biochemistry, and histopathology) were not altered either individually or in the mixture. The overall absence of individual genotoxicity did not allow us to set any type of interaction in the mixture. However, a possible toxicokinetic interaction was observed. MDPI 2023-08-03 /pmc/articles/PMC10467059/ /pubmed/37624248 http://dx.doi.org/10.3390/toxins15080491 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alonso-Jauregui, Maria
López de Cerain, Adela
Azqueta, Amaya
Rodriguez-Garraus, Adriana
Gil, Ana Gloria
González-Peñas, Elena
Vettorazzi, Ariane
In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1
title In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1
title_full In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1
title_fullStr In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1
title_full_unstemmed In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1
title_short In Vivo Genotoxicity and Toxicity Assessment of Sterigmatocystin Individually and in Mixture with Aflatoxin B1
title_sort in vivo genotoxicity and toxicity assessment of sterigmatocystin individually and in mixture with aflatoxin b1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467059/
https://www.ncbi.nlm.nih.gov/pubmed/37624248
http://dx.doi.org/10.3390/toxins15080491
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