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Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata)

Aflatoxin B1 (AFB1) is a mycotoxin often present in food. This study aimed to understand the physiological effects of AFB1 on the seabream (Sparus aurata) gastrointestinal system. In a first in vitro approach, we investigated ion transport using the short-circuit current (Isc) technique in Ussing ch...

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Autores principales: Barany, Andre, Oliva, Milagrosa, Gregório, Silvia Filipa, Martínez-Rodríguez, Gonzalo, Mancera, Juan Miguel, Fuentes, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722709/
https://www.ncbi.nlm.nih.gov/pubmed/34987413
http://dx.doi.org/10.3389/fphys.2021.741192
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author Barany, Andre
Oliva, Milagrosa
Gregório, Silvia Filipa
Martínez-Rodríguez, Gonzalo
Mancera, Juan Miguel
Fuentes, Juan
author_facet Barany, Andre
Oliva, Milagrosa
Gregório, Silvia Filipa
Martínez-Rodríguez, Gonzalo
Mancera, Juan Miguel
Fuentes, Juan
author_sort Barany, Andre
collection PubMed
description Aflatoxin B1 (AFB1) is a mycotoxin often present in food. This study aimed to understand the physiological effects of AFB1 on the seabream (Sparus aurata) gastrointestinal system. In a first in vitro approach, we investigated ion transport using the short-circuit current (Isc) technique in Ussing chambers in the anterior intestine (AI). Application of apical/luminal AFB1 concentrations of 8 and 16 μM to healthy tissues was without effect on tissue transepithelial electrical resistance (TER), and apparent tissue permeability (Papp) was measured using fluorescein FITC (4 kD). However, it resulted in dose-related effects on Isc. In a second approach, seabream juveniles fed with different AFB1 concentrations (1 and 2 mg AFB1 kg(−1) fish feed) for 85 days showed significantly reduced gill Na(+)/K(+)-ATPase (NKA) and H(+)-ATPase (HA) activities in the posterior intestine (PI). Moreover, dietary AFB1 modified Isc in the AI and PI, significantly affecting TER in the AI. To understand this effect on TER, we analyzed the expression of nine claudins and three occludins as markers of intestinal architecture and permeability using qPCR. Around 80% of the genes presented significantly different relative mRNA expression between AI and PI and had concomitant sensitivity to dietary AFB1. Based on the results of our in vitro, in vivo, and molecular approaches, we conclude that the effects of dietary AFB1 in the gastrointestinal system are at the base of the previously reported growth impairment caused by AFB1 in fish.
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spelling pubmed-87227092022-01-04 Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata) Barany, Andre Oliva, Milagrosa Gregório, Silvia Filipa Martínez-Rodríguez, Gonzalo Mancera, Juan Miguel Fuentes, Juan Front Physiol Physiology Aflatoxin B1 (AFB1) is a mycotoxin often present in food. This study aimed to understand the physiological effects of AFB1 on the seabream (Sparus aurata) gastrointestinal system. In a first in vitro approach, we investigated ion transport using the short-circuit current (Isc) technique in Ussing chambers in the anterior intestine (AI). Application of apical/luminal AFB1 concentrations of 8 and 16 μM to healthy tissues was without effect on tissue transepithelial electrical resistance (TER), and apparent tissue permeability (Papp) was measured using fluorescein FITC (4 kD). However, it resulted in dose-related effects on Isc. In a second approach, seabream juveniles fed with different AFB1 concentrations (1 and 2 mg AFB1 kg(−1) fish feed) for 85 days showed significantly reduced gill Na(+)/K(+)-ATPase (NKA) and H(+)-ATPase (HA) activities in the posterior intestine (PI). Moreover, dietary AFB1 modified Isc in the AI and PI, significantly affecting TER in the AI. To understand this effect on TER, we analyzed the expression of nine claudins and three occludins as markers of intestinal architecture and permeability using qPCR. Around 80% of the genes presented significantly different relative mRNA expression between AI and PI and had concomitant sensitivity to dietary AFB1. Based on the results of our in vitro, in vivo, and molecular approaches, we conclude that the effects of dietary AFB1 in the gastrointestinal system are at the base of the previously reported growth impairment caused by AFB1 in fish. Frontiers Media S.A. 2021-12-20 /pmc/articles/PMC8722709/ /pubmed/34987413 http://dx.doi.org/10.3389/fphys.2021.741192 Text en Copyright © 2021 Barany, Oliva, Gregório, Martínez-Rodríguez, Mancera and Fuentes. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Barany, Andre
Oliva, Milagrosa
Gregório, Silvia Filipa
Martínez-Rodríguez, Gonzalo
Mancera, Juan Miguel
Fuentes, Juan
Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata)
title Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata)
title_full Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata)
title_fullStr Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata)
title_full_unstemmed Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata)
title_short Dysregulation of Intestinal Physiology by Aflatoxicosis in the Gilthead Seabream (Sparus aurata)
title_sort dysregulation of intestinal physiology by aflatoxicosis in the gilthead seabream (sparus aurata)
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722709/
https://www.ncbi.nlm.nih.gov/pubmed/34987413
http://dx.doi.org/10.3389/fphys.2021.741192
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