Maternal sucralose exposure induces Paneth cell defects and exacerbates gut dysbiosis of progeny mice

潘尼斯电池 失调 后代 生物 肠道菌群 三氯蔗糖 断奶 免疫学 男科 胃肠道 垃圾箱 内分泌学 内科学 怀孕 生理学 小肠 医学 生物化学 食品科学 遗传学 农学
作者
Xin Dai,Chen Wang,Zixuan Guo,Yun Li,Tianyu Liu,Ge Jin,Sinan Wang,Bangmao Wang,Kui Jiang,Hailong Cao
出处
期刊:Food & Function [The Royal Society of Chemistry]
卷期号:12 (24): 12634-12646 被引量:9
标识
DOI:10.1039/d1fo02921e
摘要

Research has shown that maternal sucralose (MS) exposure alters the gut microbiota of offspring at weaning and predisposes the offspring to developing obesity, non-alcoholic fatty liver disease and metabolic syndrome later in life. However, the underlying mechanism remains unclear. Paneth cells are thought to critically influence the gut microbiota. This study aimed to investigate whether MS exposure induced Paneth cell defects and exacerbated gut dysbiosis of offspring. Female C57BL/6 mice were divided into the MS and control (water) groups during pregnancy and lactation. Progeny mice were fed a normal sucralose-free diet after weaning until adulthood. MS inhibited intestinal development and increased the expression of proinflammatory cytokines in the small intestines of 3-week-old progeny mice. MS increased the proportions of abnormal granule secretion by Paneth cells. The number of Paneth cells and mRNA expression of AMPs such as cryptdins and lysozyme were reduced in the MS group. MS disturbed the gut microbiota composition and diversity in the 3-week-old offspring mice. The relative abundances of pro-inflammatory bacteria, such as Desulfovibrionales, Helicobacter, Pasteurellales and Campylobacterales were significantly increased in the MS group, while anti-inflammatory bacteria, including Clostridium XI, were decreased. This dysbiosis continued into adulthood. These findings showed that MS exposure induced Paneth cell defects and exacerbated gut dysbiosis in offspring mice. Sucralose should be consumed with caution, especially during pregnancy and in early life.
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