Probiotics may delay the progression of nonalcoholic fatty liver disease by restoring the gut microbiota structure and improving intestinal endotoxemia

肠道菌群 TLR4型 非酒精性脂肪肝 脂多糖 益生菌 脂肪肝 菌群(微生物学) 失调 免疫学 炎症 微生物群 生物 炎症性肠病 胰岛素抵抗 医学 肠道通透性 微生物学 鼠李糖乳杆菌 胆汁酸 内科学 疾病 细菌 遗传学
作者
Li Xue,Juntao He,Ning Gao,Xiaolan Lu,Ming Li,Xiaokang Wu,Zeshi Liu,Yanling Jin,Jiali Liu,Jiru Xu,Yan Geng
出处
期刊:Scientific Reports [Springer Nature]
卷期号:7 (1) 被引量:192
标识
DOI:10.1038/srep45176
摘要

Abstract Gut-derived bacterial lipopolysaccharide (LPS) and subsequent hepatic toll-like receptor 4 (TLR4) activation have been recognized to be involved in the onset of diet-induced nonalcoholic fatty liver disease (NAFLD), but little is known about the variation of LPS and TLR4 during the progression of NAFLD. Probiotics were able to inhibit proliferation of harmful bacteria and improve gastrointestinal barrier function. However, it’s unclear whether LPS/TLR4 is involved in the protection effect of probiotics on NAFLD. In this study, we described characteristic of gut microbiota structure in the progression of NAFLD, and we also analyzed the relationship between gut microbiota and LPS/TLR4 in this process. Furthermore, we applied probiotics intervention to investigate the effect of probiotics on gut flora structure, intestinal integrity, serum LPS, liver TLR4 and liver pathology. Our results showed that serum LPS and liver TLR4 were highly increased during progression of NAFLD, with gut flora diversity and gut mircobiological colonization resistance (B/E) declining. Furthermore, probiotics could improve gut microbiota structure and liver pathology. Probiotics could also downregulate serum LPS and liver TLR4. Our results suggested that both gut flora alteration and endotoxemia may be involved in the progression of NAFLD. Probiotics may delay the progression of NAFLD via LPS/TLR4 signaling.
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