RESUMO
Ionic liquid tetrafluoroborated-1-tetradecyl-3-methylimidazole salt ([C14mim]BF4) immunotoxicity was investigated in rats using three exposure groups (12.5, 25, and 50 mg kg-1), one recovery group (50 mg kg-1), and a control group without any treatment. The findings demonstrated that, at low doses, [C14mim]BF4 could raise WBC, NEU, and MID and lysozyme levels as well as spleen T-lymphocyte stimulation index in rats, however at high doses, the aforementioned indices were dramatically lowered. As the dose was raised, the proportion of RBC and PLT in the blood as well as CD4+ and CD8+ in the spleen increased, but the quantity of immunoglobulin IgG, IgA, and IgM in the serum as well as the number of NK cells in the spleen considerably dropped. Even though there were varying degrees of improvement 30 days after ceasing exposure, all these changes were unable to return to normal, and the number of NK cells was further decreased. The study demonstrates that [C14mim]BF4 can damage the specific immunity and non-specific immunity of rats, and cause immune dysfunction.
Assuntos
Imidazóis , Líquidos Iônicos , Baço , Animais , Baço/efeitos dos fármacos , Baço/imunologia , Líquidos Iônicos/toxicidade , Masculino , Ratos , Imidazóis/toxicidade , Células Matadoras Naturais/efeitos dos fármacos , Células Matadoras Naturais/imunologia , Ratos Sprague-Dawley , Muramidase , Linfócitos T/efeitos dos fármacos , Linfócitos T/imunologiaRESUMO
The purpose of this study was to elucidate the mechanism underlying toxicity in the livers of male and female rats after treatment with 1-tetradecyl-3-methylimidazolium tetrafluoroborate ([C14mim]BF4, 0 [control], 12.5, 25, or 50 mg/kg) for 90 days. The results showed that [C14mim]BF4 exposure led to a high level of ROS and MDA in rat livers and the lower expression of Nrf2 and its downstream related antioxidant proteins. In addition, the expression of NF-κB p65 and the levels of inflammatory cytokines were upregulated in exposure groups rats' liver. After 30 days of cessation of exposure, the liver injury of rats in the 50 mg/kg exposure group was alleviated, and the above indicators were improved to varying degrees. The paper shows that [C14mim]BF4 could damage rat liver through oxidative stress and inflammatory pathway.
