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Gastrointestinal Degradation and Toxicity of Disinfection Byproducts in Drinking Water Using In Vitro Models and the Roles of Gut Microbiota.
Yin, Jinbao; Li, Dingxin; Zheng, Tianming; Hu, Bin; Wang, Peifang.
Afiliación
  • Yin J; Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes of Ministry of Education, College of Environment, Hohai University, 1 Xikang Road, Nanjing 210098, China.
  • Li D; Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes of Ministry of Education, College of Environment, Hohai University, 1 Xikang Road, Nanjing 210098, China.
  • Zheng T; Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes of Ministry of Education, College of Environment, Hohai University, 1 Xikang Road, Nanjing 210098, China.
  • Hu B; Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes of Ministry of Education, College of Environment, Hohai University, 1 Xikang Road, Nanjing 210098, China.
  • Wang P; Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes of Ministry of Education, College of Environment, Hohai University, 1 Xikang Road, Nanjing 210098, China.
Environ Sci Technol ; 57(43): 16219-16231, 2023 10 31.
Article en En | MEDLINE | ID: mdl-37847491
Disinfection byproducts (DBPs) in drinking water are mainly exposed to the human body after oral ingestion and degradation in the gastrointestinal tract. The role of gastrointestinal degradation in the toxic effects of DBPs still needs further investigation. In this study, the degradation of five categories of DBPs (22 DBPs) in the stomach and small intestine was investigated based on a semicontinuous steady-state gastrointestinal simulation system, and 22 DBPs can be divided into three groups based on their residual proportions. The degradation of chloroacetonitrile (CAN), dibromoacetic acid (DBAA), and tetrabromopyrrole (FBPy) was further analyzed based on the Simulator of the Human Intestinal Microbial Ecosystem inoculating the gut microbiota, and approximately 60% of CAN, 45% of DBAA, and 80% of FBPy were degraded in the stomach and small intestine, followed by the complete degradation of remaining DBPs in the colon. Meanwhile, gastrointestinal degradation can reduce oxidative stress-mediated DNA damage and apoptosis induced by DBPs in DLD-1 cells, but the toxicity of DBPs did not disappear with the complete degradation of DBPs, possibly because of their interferences on gut microbiota. This study provides new insights into investigating the gastrointestinal toxic effects and mechanisms of DBPs through oral exposure.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Contaminantes Químicos del Agua / Agua Potable / Purificación del Agua / Desinfectantes / Microbioma Gastrointestinal Límite: Humans Idioma: En Revista: Environ Sci Technol Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Contaminantes Químicos del Agua / Agua Potable / Purificación del Agua / Desinfectantes / Microbioma Gastrointestinal Límite: Humans Idioma: En Revista: Environ Sci Technol Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos