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Saccharin induced liver inflammation in mice by altering the gut microbiota and its metabolic functions

Bian, Xiaoming, Tu, Pengcheng, Chi, Liang, Gao, Bei, Ru, Hongyu, Lu, Kun
Food and chemical toxicology 2017 v.107 pp. 530-539
bacterial toxins, beverages, biochemical pathways, drinking water, food additives, human health, inducible nitric oxide synthase, inflammation, intestinal microorganisms, liver, males, metabolites, metabolomics, mice, pathogen-associated molecular patterns, ribosomal RNA, saccharin, sequence analysis, toxicology, tumor necrosis factor-alpha
Maintaining the balance of the gut microbiota and its metabolic functions is vital for human health, however, this balance can be disrupted by various external factors including food additives. A range of food and beverages are sweetened by saccharin, which is generally considered to be safe despite controversial debates. However, recent studies indicated that saccharin perturbed the gut microbiota. Inflammation is frequently associated with disruptions of the gut microbiota. The aim of this study is to investigate the relationship between host inflammation and perturbed gut microbiome by saccharin. C57BL/6J male mice were treated with saccharin in drinking water for six months. Q-PCR was used to detect inflammatory markers in mouse liver, while 16S rRNA gene sequencing and metabolomics were used to reveal changes of the gut microbiota and its metabolomic profiles. Elevated expression of pro-inflammatory iNOS and TNF-α in liver indicated that saccharin induced inflammation in mice. The altered gut bacterial genera, enriched orthologs of pathogen-associated molecular patterns, such as LPS and bacterial toxins, in concert with increased pro-inflammatory metabolites suggested that the saccharin-induced liver inflammation could be associated with the perturbation of the gut microbiota and its metabolic functions.