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Intermittent Exposure to Aflatoxin B(1) Did Not Affect Neurobehavioral Parameters and Biochemical Markers of Oxidative Stress

Aflatoxin B(1) (AFB(1)) is the most common toxic mycotoxin that contaminates food. The treatment of its intoxication and the management of contaminations are a constant subject of health agendas worldwide. However, such efforts are not always enough to avoid population intoxication. Our objective wa...

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Detalles Bibliográficos
Autores principales: Braga, Ana Claudia Monteiro, Souto, Naieli Schiefelbein, Cabral, Fernanda Licker, Dassi, Micheli, Rosa, Érica Vanessa Furlan, Guarda, Naiara dos Santos, Royes, Luiz Fernando Freire, Fighera, Michele Rechia, Moresco, Rafael Noal, Oliveira, Mauro Schneider, Sari, Marcel Henrique Marcondes, Furian, Ana Flávia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046455/
https://www.ncbi.nlm.nih.gov/pubmed/36979196
http://dx.doi.org/10.3390/brainsci13030386
Descripción
Sumario:Aflatoxin B(1) (AFB(1)) is the most common toxic mycotoxin that contaminates food. The treatment of its intoxication and the management of contaminations are a constant subject of health agendas worldwide. However, such efforts are not always enough to avoid population intoxication. Our objective was to investigate whether intermittent exposure to AFB(1) would cause any impairment in biochemical and behavioral parameters, intending to simulate an irregular consumption. Male Wistar rats received four AFB(1) administrations (250 μg/kg) by intragastric route separated by a 96-h interval. Toxicity was evaluated using behavioral tests (open field, object recognition, nest construction, marble burying, and splash test), biochemical markers of oxidative stress (cerebral cortex, hippocampus, liver, and kidneys), and plasma parameters of hepatic and renal functions. The intermittent exposure caused no modification in body weight gain as well as in organ weight. Both control and AFB(1) groups presented similar profiles of behavior to all tests performed. Furthermore, AFB(1) administrations alter neither antioxidant defenses nor markers of oxidation in all assayed tissues and in the plasma markers of hepatic and renal functions. Therefore, AFB(1) intermittent administration did not cause its common damage from exposure to this toxicant, which must be avoided, and additional studies are required.