Maternal sucralose intake alters gut microbiota of offspring and exacerbates hepatic steatosis in adulthood

失调 后代 脂肪变性 生物 肠道菌群 内科学 丁酸盐 非酒精性脂肪肝 内分泌学 脂质代谢 断奶 脂肪肝 生理学 免疫学 怀孕 医学 疾病 生物化学 遗传学 发酵
作者
Xin Dai,Zixuan Guo,Danfeng Chen,Lu Li,Xueli Song,Tianyu Liu,Ge Jin,Yun Li,Yi Liu,Aihemaiti Ajiguli,Cheng Yang,Bangmao Wang,Hailong Cao
出处
期刊:Gut microbes [Landes Bioscience]
卷期号:11 (4): 1043-1063 被引量:61
标识
DOI:10.1080/19490976.2020.1738187
摘要

Background Nonalcoholic fatty liver disease (NAFLD) is considered to be associated with diet and gut dysbiosis. Excessive sucralose can induce gut dysbiosis and negatively affect host health. Maternal diet shapes the microbial communities of neonate and this effect continues in later life. We aimed to investigate the effects of maternal sucralose (MS) intake on the susceptibility of offspring to hepatic steatosis in adulthood.Methods C57BL/6 pregnant mice were randomized into MS group (MS during gestation and lactation) and maternal control (MC) group (MC diet). After weaning, all offspring were fed a control diet until 8 weeks of age, and then treated with a high-fat diet (HFD) for 4 weeks. The intestinal development, mucosal barrier function, and gut microbiota were assessed in the 3-week-old offspring. Moreover, the severity of hepatic steatosis, serum biochemistry, lipid metabolism, and gut microbiota was then assessed in the 12th week.Results MS significantly inhibited intestinal development and disrupted barrier function in 3-week-old offspring. MS also induced intestinal low-grade inflammation, significantly changed the compositions and diversity of gut microbiota including reducing butyrate-producing bacteria and cecal butyrate production with down-regulation of GPR43. Mechanically, blocking GPR43 blunted the anti-inflammatory effect of one of the butyrate-producing bacteria, Clostridium butyricum in vitro. After HFD treatment, MS exacerbated hepatic steatosis, and disturbed fatty acid biosynthesis and metabolism, accompanied by inducing gut dysbiosis compared with MC group.Conclusions MS intake inhibits intestinal development, induces gut dysbiosis in offspring through down-regulation of GPR43, and exacerbates HFD-induced hepatic steatosis in adulthood.

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