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Hepatic, Metabolic, and Toxicity Evaluation of Repeated Oral Administration of SnS2 Nanoflowers in Mice.
Bai, Disi; Li, Qingzhao; Xiong, Yanjie; Wang, Chao; Shen, Peijun; Bai, Liyuan; Yuan, Lu; Wu, Ping.
Afiliação
  • Bai D; Department of Applied Physics, Institute of Advanced Materials Physics, Tianjin Key Laboratory of Low Dimensional Materials Physics and Preparing Technology, Faculty of Science, Tianjin University, Tianjin 300072, People's Republic of China.
  • Li Q; School of Public Health, North China University of Science and Technology, Tangshan, Hebei 063000, People's Republic of China.
  • Xiong Y; Department of Pathology, North China University of Science and Technology Affiliated Hospital, Tangshan, Hebei 063000, People's Republic of China.
  • Wang C; Department of Applied Physics, Institute of Advanced Materials Physics, Tianjin Key Laboratory of Low Dimensional Materials Physics and Preparing Technology, Faculty of Science, Tianjin University, Tianjin 300072, People's Republic of China.
  • Shen P; Center of Environmental Monitoring of Tangshan, Tangshan, Hebei 063000, People's Republic of China.
  • Bai L; Tangshan Environmental Monitoring Center of Heibei Province, Tangshan, Hebei 063000, People's Republic of China.
  • Yuan L; School of Public Health, North China University of Science and Technology, Tangshan, Hebei 063000, People's Republic of China.
  • Wu P; Department of Applied Physics, Institute of Advanced Materials Physics, Tianjin Key Laboratory of Low Dimensional Materials Physics and Preparing Technology, Faculty of Science, Tianjin University, Tianjin 300072, People's Republic of China.
Toxicol Sci ; 164(2): 501-511, 2018 08 01.
Article em En | MEDLINE | ID: mdl-29722875
ABSTRACT
Tin sulfide (SnS2) nanoflowers (NFs) with highly photocatalytic activity for wastewater treatment may lead to potential health hazards via oral routes of human exposure. No studies have reported the hepatic effects of SnS2 NFs on the metabolic function and hepatotoxicity. In this study, we examined the hepatic effects of the oral administration of SnS2 NFs (250-1000 mg/kg) to ICR mice for 14 days, with the particle size ranging from 50 to 200 nm. Serum and liver tissue samples were assayed using biochemical analysis, liver histopathology and metabolic gene expression. The different sizes of SnS2 NFs (250 mg/kg dose), such as 50, 80, and 200 nm, did not induce any adverse hepatic effect related to biochemical parameters or histopathology in the treated mice compared with controls. The oral administration of 50-nm SnS2 NFs at doses of 250, 500, and 1000 mg/kg for 14 days produced dose-dependent hepatotoxicity and inflammatory responses in treated mice. Furthermore, the expression of metabolic genes in the liver tissues was altered, supporting the SnS2 NF-related hepatotoxic phenotype. The oral administration of SnS2 NFs also produced abnormal microstructures in the livers of the treated mice. Taken together, these data indicate that the increased risk of hepatotoxicity in SnS2 NF-treated mice was independent of the particle size but was dependent on their dose. The no-observed-adverse effect level was <250 mg/kg for the 50-nm SnS2 NFs. Our study provides an experimental basis for the safe application of SnS2 NFs.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sulfetos / Compostos de Estanho / Nanoestruturas / Doença Hepática Induzida por Substâncias e Drogas / Fígado Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sulfetos / Compostos de Estanho / Nanoestruturas / Doença Hepática Induzida por Substâncias e Drogas / Fígado Idioma: En Ano de publicação: 2018 Tipo de documento: Article