Impact of a Single Oral Acute Dose of Aflatoxin B₁ on Liver Function/Cytokines and the Lymphoproliferative Response in C57Bl/6 Mice.
Angélica Tieme IshikawaElisa Yoko HirookaPaula Leonello Alvares E SilvaAna Paula Frederico Rodrigues Loureiro BracarenseKarina Keller Marques da Costa FlaibanClaudia Yuri AkagiOsamu KawamuraMarcio Carvalho da CostaEiko Nakagawa ItanoPublished in: Toxins (2017)
Aflatoxin B₁ (AFB₁), a mycotoxin found in food and feed, exerts harmful effects on humans and animals. The liver is the earliest target of AFB₁, and its effects have been evaluated in animal models exposed to acute or chronic doses. Considering the possibility of sporadic ingestion of AFB₁-contaminated food, this study investigated the impact of a single oral dose of AFB₁ on liver function/cytokines and the lymphoproliferative response in mice. C57BL/6 mice were treated with a single oral AFB₁ dose (44, 442 or 663 μg AFB₁/kg of body weight) on the first day. Liver function (ALT, γ-GT, and total protein), cytokines (IL-4, IFN-γ, and IL-17), histopathology, and the spleen lymphoproliferative response to mitogens were evaluated on the 5th day. Although AFB₁ did not produce any significant changes in the biochemical parameters, 663 μg AFB₁/kg-induced hepatic upregulation of IL-4 and IFN-γ, along with liver tissue injury and suppression of the lymphoproliferative response to ConA (p < 0.05). In conclusion, a single oral dose of AFB₁ exposure can induce liver tissue lesions, liver cytokine modulation, and immune suppression in C57BL/6 mice.
Keyphrases
- epstein barr virus
- body weight
- liver failure
- drug induced
- immune response
- cell proliferation
- intensive care unit
- heavy metals
- oxidative stress
- metabolic syndrome
- drinking water
- late onset
- poor prognosis
- type diabetes
- high resolution
- adipose tissue
- wild type
- diabetic rats
- newly diagnosed
- diffuse large b cell lymphoma
- high glucose
- human health