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Effects of Inulin Propionate Ester on Obesity-Related Metabolic Syndrome and Intestinal Microbial Homeostasis in Diet-Induced Obese Mice

机译:菊粉丙酸酯对肥胖相关的代谢综合征和肠道微生物稳态在饮食诱导的肥胖小鼠中的影响

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Short-chain fatty acid (SCFA) plays an important role in improving obesity and related metabolic syndrome induced by high-fat diet. We used the prepared inulin propionate ester (IPE) as a system for the targeted release of propionate to the colon to elucidate the role of IPE in regulating obesity and metabolic syndrome, and intestinal microbial homeostasis, in diet-induced obese mice. With this strategy, IPE significantly increased the SCFA contents in the colon and resulted in significant body weight reduction, insulin resistance amelioration, and gastrointestinal hormone (glucagon-like peptide and peptide YY) secretion (P < 0.05). The IPE intervention reduced liver fatty accumulation, which improved obesity-related fatty liver disease (P < 0.05). IPE supplementation increased the richness and diversity of the microbial community and altered bacterial population at both the phylum and family level. Intestinal microbial results showed that the relative abundance of Desulfovibrionaceae and Erysipelotrichaceae, which promote the production of inflammatory factors, was reduced. Our results demonstrate that IPE can be used as an effective strategy for delivering propionate to obese mice colon, which can ameliorate obesity and associated metabolic syndrome and modify intestinal microbial homeostasis.
机译:短链脂肪酸(SCFA)在改善高脂饮食诱导的肥胖症和相关代谢综合征方面发挥着重要作用。我们使用制备的菊粉丙酸酯(IPE)作为靶向丙酸酯的丙酸释放的系统,以阐明IPE在饮食诱导的肥食小鼠中调节肥胖和代谢综合征和肠道微生物稳态的作用。通过这种策略,IPE显着增加了结肠中的SCFA含量,导致体重减轻,胰岛素抵抗改善和胃肠激素(胰高血糖素样肽和肽YY)分泌( P <0.05)。 IPE干预降低了肝脏脂肪积累,其改善了肥胖相关的脂肪肝疾病( P <0.05)。 IPE补充增加了微生物群落的丰富性和多样性,并且在门口和家庭层面都改变了细菌种群。肠道微生物研究结果表明,促进炎症因素的产生的脱硫纤维痤疮和饮食性的相对丰度。我们的结果表明,IPE可以用作赋予肥胖小鼠结肠替代的有效策略,这可以改善肥胖症和相关的代谢综合征,并改变肠道微生物稳态。

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