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8:2 Fluorotelomer alcohol causes immunotoxicity and liver injury in adult male C57BL/6 mice
8:2 Fluorotelomer alcohol (8:2 FTOH) is widely used in houseware and industrial goods and is ubiquitous in the surrounding environment. 8:2 FTOH has been linked to hepatoxicity, nephrotoxicity, and reproductive toxicity, as well as endocrine‐disrupting effects. However, as of yet, the research regarding immunotoxicity of 8:2 FTOH remains largely limited. In the present study, adult male C57BL/6 mice were administered with 10, 30, and 100 mg/kg/d 8:2 FTOH by gavage for 28 days to investigate its immunotoxicity in vivo. The results showed that exposure to 8:2 FTOH caused increases in liver weight and histological changes in the liver, including vacuolation, cell swelling, immune cell infiltration, karyopyknosis and nuclear swelling. No histological change in either the spleen or the thymus was observed after administration of 8:2 FTOH. In addition, exposure to 8:2 FTOH reduced the concentration of IL‐1β in serum, and mRNA levels of IL‐1β, IL‐6, and TNF‐α in both the thymus and spleen. CXCL‐1 mRNA expression was downregulated in both the liver and thymus after 8:2 FTOH administration, while only IL‐1β mRNA expression was upregulated in the liver. Moreover, the exposure of primary cultured splenocytes to 8:2 FTOH inhibited the ConA‐stimulated proliferation of splenocytes at concentrations of 30 and 100 μM, and the LPS‐stimulated proliferation of splenocytes at 100 μM. Furthermore, 8:2 FTOH inhibited the level of secreted IFN‐γ in ConA‐stimulated splenocytes. The results obtained in the study demonstrated that 8:2 FTOH posed potential immunotoxicity and liver injury in mice. Our findings will provide novel data for the health risk assessment of 8:2 FTOH.
8:2 Fluorotelomer alcohol causes immunotoxicity and liver injury in adult male C57BL/6 mice
8:2 Fluorotelomer alcohol (8:2 FTOH) is widely used in houseware and industrial goods and is ubiquitous in the surrounding environment. 8:2 FTOH has been linked to hepatoxicity, nephrotoxicity, and reproductive toxicity, as well as endocrine‐disrupting effects. However, as of yet, the research regarding immunotoxicity of 8:2 FTOH remains largely limited. In the present study, adult male C57BL/6 mice were administered with 10, 30, and 100 mg/kg/d 8:2 FTOH by gavage for 28 days to investigate its immunotoxicity in vivo. The results showed that exposure to 8:2 FTOH caused increases in liver weight and histological changes in the liver, including vacuolation, cell swelling, immune cell infiltration, karyopyknosis and nuclear swelling. No histological change in either the spleen or the thymus was observed after administration of 8:2 FTOH. In addition, exposure to 8:2 FTOH reduced the concentration of IL‐1β in serum, and mRNA levels of IL‐1β, IL‐6, and TNF‐α in both the thymus and spleen. CXCL‐1 mRNA expression was downregulated in both the liver and thymus after 8:2 FTOH administration, while only IL‐1β mRNA expression was upregulated in the liver. Moreover, the exposure of primary cultured splenocytes to 8:2 FTOH inhibited the ConA‐stimulated proliferation of splenocytes at concentrations of 30 and 100 μM, and the LPS‐stimulated proliferation of splenocytes at 100 μM. Furthermore, 8:2 FTOH inhibited the level of secreted IFN‐γ in ConA‐stimulated splenocytes. The results obtained in the study demonstrated that 8:2 FTOH posed potential immunotoxicity and liver injury in mice. Our findings will provide novel data for the health risk assessment of 8:2 FTOH.
8:2 Fluorotelomer alcohol causes immunotoxicity and liver injury in adult male C57BL/6 mice
Wang, Xia (Autor:in) / Kong, Baida (Autor:in) / He, Bingnan (Autor:in) / Wei, Lai (Autor:in) / Zhu, Jianbo (Autor:in) / Jin, Yuanxiang (Autor:in) / Shan, Yudong (Autor:in) / Wang, Weitao (Autor:in) / Pan, Chunqiang (Autor:in) / Fu, Zhengwei (Autor:in)
Environmental Toxicology ; 34 ; 141-149
01.02.2019
9 pages
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
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