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Active phase prebiotic feeding alters gut microbiota, induces weight-independent alleviation of hepatic steatosis and serum cholesterol in high-fat diet-fed mice

机译:活性期益生喂养改变了肠道微生物酵母,诱导重量依赖于肝脏脂肪变性和高脂饮食喂养小鼠的血清胆固醇

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Growing evidence suggests that prebiotics may induce weight loss and alleviate non-alcoholic fatty liver disease (NAFLD) via modulation of the gut microbiota. However, key members of the gut microbiota that may mediate the beneficial effects of prebiotics remain elusive. Here, we find that restricted prebiotic feeding during active phase (HF-ARP) induced weight-independent alleviation of liver steatosis and reduced serum cholesterol in high-fat diet (HF) fed mice more significantly than unrestricted feeding (HF-UP). HF-ARP mice also showed concomitantly altered gut microbiota structure that was different from HF-UP group along with significantly increased production of total short-chain fatty-acids (SCFAs). Amplicon sequence variants (ASVs) were clustered into co-abundant groups (CAGs) as potential functional groups that may respond distinctively to prebiotic consumption and prebiotic feeding regime. Prebiotic feeding induces significant alterations in CAG abundances by day 7. Eight of 32 CAGs were promoted by prebiotics, including CAG17 with the most abundant ASV from Parabacteroides, CAG22 with Bacteroides thetaiotamicron and CAG32 with Fecalibaculum and Akkermansia . Among the prebiotic-promoted CAGs, CAG20 with ASVs from Lachnospiraceae and CAG21 with ASVs from Bifidobacterium and Lachnospiraceae were significantly enhanced in HF-ARP compared to HF-UP. Moreover, most of the prebiotic-promoted CAGs were also significantly associated with improvements in hepatic steatosis, reduction in serum cholesterol and increased cecal propionate production. Together, these results suggest that the impact of prebiotics on weight-independent alleviation of liver steatosis and cholesterol-lowering effect can be optimized by restricting prebiotic intake to active phase and is associated with a distinct change of gut microbiota with increased SCFA production.
机译:日益增长的证据表明,益生元可以通过调节肠道微生物的调节诱导体重减轻和缓解非酒精脂肪肝疾病(NAFLD)。然而,肠道微生物群的关键成员可能介绍益生元的有益效果仍然难以捉摸。在这里,我们发现在活性期(HF-ARP)期间的限制益生元喂养诱导肝脏脂肪变量减轻肝脏脂肪变性,并在高脂饮食中减少血清胆固醇(HF)小鼠比不受限制的饲养(HF-UP)更显着。 HF-ARP小鼠还表现出与HF-UP组不同的肠道微生物群结构以及显着增加的总短链脂肪酸(SCFA)的产生。扩增子序列变体(ASV)聚集成共同的群体(CAG),作为潜在的官能团,可与益生元消费和益生元饲料制度鲜明。益生元饲料在第7天诱导CAG丰富的显着改变。留下益生元素促进了32个CAG,包括CAG17,从ParaMacteropes,CAG22与菌菌和嗜虫草的菌株和CAG32具有菌菌和CAG32的CAG17。与HF-ARP相比,与Lachnospiraceae和来自双歧杆菌和Lachnospiraceae的ASVs的CAG21的CAG20在HF-ARP中显着提高了HF-ARP的CAG20。此外,大多数益生菌促进的CAG也与肝脏脂肪变性的改善有显着相关,血清胆固醇还原并增加肠丙酸盐产生。这些结果表明,通过限制益生元摄入至活性阶段,可以优化益生元对肝脏脂肪变量和降低胆固醇降低效果的影响,并且与肠道微生物症的不同变化有关的SCFA生产。

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