T-2 toxin and zearalenone influence on the pro-inflammatory cytokines content in liver cells primary cultures
Автор: Samsonov A., Makaeva A., Mishina N., Valiullin L., Yarullin A.
Журнал: Вестник Красноярского государственного аграрного университета @vestnik-kgau
Рубрика: Зоотехния и ветеринария
Статья в выпуске: 4, 2024 года.
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Mycotoxins are dangerous metabolites of fungi that are found in feed and food products. Combinations of several Fusarium mycotoxins, including T-2 toxin and zearalenone, are often found in contaminated cereal crops. The liver plays a crucial role in detoxification processes and is one of the main targets of mycotoxins. The purpose of research is to study the effect of T-2 toxin and zearalenone on the production of pro-inflammatory cytokines interleukin-6 (IL-6) and interleukin-8 (IL-8) in primary cultures of chicken liver cells. The production of pro-inflammatory cytokines IL-6 and IL-8 was studied using ELISA kits produced by Vector. It was found that the concentration of the pro-inflammatory cytokine IL-6 was increased as a result of exposure to T-2 mycotoxin at both 100.0 nmol/dm3 and 1000.0 nmol/dm3 in hepatocyte culture, after 12 hours of incubation as a result of rapid toxic shock, but not at a toxin concentration of 10.0 nmol/dm3. When exposed to T-2 toxin for 24 hours, an adaptive response occurred and no significant differences were found. Significant differences in the concentration of IL-8 were found after 24 hours of incubation, compared to the control. When similar concentrations of zearalenone were added, no significant changes in the concentrations of the cytokines IL-6 and IL-8 were observed, except in the case of the maximum concentration of the toxin. When toxins were introduced together, the dynamics of IL-6 content was similar to that of T-2 toxin, but no potentiating effect was recorded. The content of IL-8 changed more than with the addition of monomycotoxin.
T-2 toxin, zearalenone, primary liver cell culture, proinflammatory cytokines, il-6, il-8
Короткий адрес: https://sciup.org/140306654
IDR: 140306654 | DOI: 10.36718/1819-4036-2024-4-102-110