Different depths of food restriction and high-fat diet refeeding in mice impact host obesity and metabolic phenotypes with correlative changes in the gut microbiota

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL MedComm Pub Date : 2024-07-17 DOI:10.1002/mco2.641
Jiaqi Xu, Huangru Xu, Feiyan Yang, Yawen Xie, Fangfang Cai, Siyu Mao, Min Lu, Hongqin Zhuang, Zi-Chun Hua
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Abstract

Overweight and obesity affect almost 2 billion adults worldwide, and food restriction (FR) is commonly used to reduce body fat. Whether refeeding (Re) after FR at different ages and to different degrees leads to overweight and its possible mechanisms are uncertain. In this study, adult and young mice were both restricted to 15% and 40% of their casual food intake, and then were fed 60% high-fat chow (FR15%–Re, FR40%–Re), whereas the control groups(CON) consumed high-fat or normal food throughout, respectively. The results of the study suggest that mild FR-heavy feeding may lead to more significant abnormal fat accumulation, liver damage, and increased recruitment of intestinal inflammatory factors and immune cells in mice of different ages and involves multiple types of alterations in the gut microbiota. Further fecal transplantation experiments as well as serum and liver enzyme-linked immunosorbent assay experiments preliminarily suggest that the link between lipid metabolism and inflammatory responses and the gut microbiota may be related to the regulation of the gut and live by Lipopolysaccharides(LPS) and Peroxisome Proliferator-Activated Receptor-Alpha(PPAR-α). In addition, our study may also serve as a reference for studying obesity prevention and treatment programs at different ages.

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小鼠不同程度的食物限制和高脂饮食再喂养会影响宿主的肥胖和代谢表型,并与肠道微生物群的变化相关。
超重和肥胖影响着全球近 20 亿成年人,而食物限制(FR)通常用于减少体内脂肪。不同年龄和不同程度的限食后再喂食(Re)是否会导致超重及其可能的机制尚不确定。在这项研究中,成年小鼠和幼年小鼠都被限制了15%和40%的正常食物摄入量,然后被喂食60%的高脂肪饲料(FR15%-Re,FR40%-Re),而对照组(CON)则在整个过程中分别摄入高脂肪或正常食物。研究结果表明,轻度高FR饲喂可能会导致不同年龄的小鼠出现更明显的异常脂肪积累、肝脏损伤、肠道炎症因子和免疫细胞募集增加,并涉及肠道微生物群的多种类型改变。进一步的粪便移植实验以及血清和肝脏酶联免疫吸附实验初步表明,脂质代谢和炎症反应与肠道微生物群之间的联系可能与脂多糖(LPS)和过氧化物酶体增殖激活受体α(PPAR-α)对肠道和生命的调控有关。此外,我们的研究还可为研究不同年龄段的肥胖预防和治疗方案提供参考。
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审稿时长
10 weeks
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