Chronic exposure to fungicide propamocarb induces bile acid metabolic disorder and increases trimethylamine in C57BL/6J mice

• Published in: The Science of the total environment Vol. 642; pp. 341 - 348
• Main Authors: Wu, Sisheng, Luo, Ting, Wang, Siyu, Zhou, Jicong, Ni, Yingchun, Fu, Zhengwei, Jin, Yuanxiang
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15-11-2018
• Subjects: Animals; Bile acids; Bile Acids and Salts - metabolism; Carbamates - toxicity; Energy metabolism; Gut microbiota; Liver; Metabolic Diseases - chemically induced; Methylamines - metabolism; Mice; Mice, Inbred C57BL; Propamocarb; Toxicity Tests; Trimethylamine; Gut microbiota; Energy metabolism; Bile acids; Trimethylamine; Propamocarb
• ISSN: 0048-9697; 1879-1026
• DOI: 10.1016/j.scitotenv.2018.06.084

Propamocarb (PM) is a widely used fungicide that affects lipid biosynthesis in fungi. In this study, we explored the effects of PM on mouse metabolism and gut microbiota-related pathways by exposing C57BL/6J mice to 1, 3, and 10 mg/L PM through drinking water for a duration of 10 weeks. We found that hepatic bile acids (BAs) were considerably increased in the PM-treated group. The transcription of genes related to BA synthesis and transportation were also markedly altered in the liver and the ileum; accordingly, serous BA profiles were changed. BAs are tightly associated with energy metabolism and the gut microbiota; as expected, we observed that hepatic glycolysis; β-oxidation; fatty acid transportation, release and synthesis; and triacylglycerol synthesis and transportation were significantly altered at the transcriptional level. Gut microbial community structures were significantly changed both in cecal contents and feces. Using Linear discriminant analysis Effect Size (LEfSe), we found that Chloroflexi, Bacteroidetes and Actinobacteria phyla; Prevotellaceae, Odoribacteraceae and Porphyromonadaceae families; and Butyricimonas, Oscillospira, Parabacteroides, Prevotella and Dorea genera enriched in PM-treated mice. Fecal metabolites involved in energy metabolism were likewise altered. In addition, the atherosclerosis-promoting molecule trimethylamine was significantly increased in feces, which induced a disturbance in the cardiac NO/NOS pathway and an increase in NF-κB transcriptional levels. Our findings indicated that chronic PM exposure induced disorders in enterohepatic metabolism and had potential to increase the risk of cardiovascular disease.
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•Chronic propamocarb exposure induced gut microbiota dysbiosis in mice.•Chronic propamocarb exposure caused energy metabolism disorder in mice.•Chronic propamocarb exposure induced bile acid metabolic disorder in mice.•Chronic propamocarb exposure may increase the risk of cardiovascular disease in mice.