共生元驱动的代谢紊乱改善与饮食诱导肥胖小鼠肠道微生物组的变化有关。
Synbiotic-driven improvement of metabolic disturbances is associated with changes in the gut microbiome in diet-induced obese mice.
机构信息
School of Life Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.
Research Unit Analytical BioGeoChemistry, HelmholtzZentrum München, Neuherberg, Germany.
出版信息
Mol Metab. 2019 Apr;22:96-109. doi: 10.1016/j.molmet.2019.01.012. Epub 2019 Feb 5.
OBJECTIVE
The gut microbiota is an important influencing factor of metabolic health. Although dietary interventions with probiotics, prebiotics, and synbiotics can be effective means to regulate obesity and associated comorbidities, the underlying shifts in gut microbial communities, especially at the functional level, have not been characterized in great details. In this study, we sought to investigate the effects of synbiotics on the regulation of gut microbiota and the alleviation of high-fat diet (HFD)-induced metabolic disorders in mice.
METHODS
Specific pathogen-free (SPF) male C57BL/6J mice were fed diets with either 10% (normal diet, ND) or 60% (high-fat diet, HFD) of total calories from fat (lard). Dietary interventions in the HFD-fed mice included (i) probiotic (Bifidobacterium animalis subsp. lactis and Lactobacillus paracasei subsp. paracasei DSM 46331), (ii) prebiotic (oat β-glucan), and (iii) synbiotic (a mixture of i and ii) treatments for 12 weeks. Besides detailed characterization of host metabolic parameters, a multi-omics approach was used to systematically profile the microbial signatures at both the phylogenetic and functional levels using 16S rRNA gene sequencing, metaproteomics and targeted metabolomics analysis.
RESULTS
The synbiotic intervention significantly reduced body weight gain and alleviated features of metabolic complications. At the phylogenetic level, the synbiotic treatment significantly reversed HFD-induced changes in microbial populations, both in terms of richness and the relative abundance of specific taxa. Potentially important species such as Faecalibaculum rodentium and Alistipes putredinis that might mediate the beneficial effects of the synbiotic were identified. At the functional level, short-chain fatty acid and bile acid profiles revealed that all dietary interventions significantly restored cecal levels of acetate, propionate, and butyrate, while the synbiotic treatment reduced the bile acid pools most efficiently. Metaproteomics revealed that the effects of the synbiotic intervention might be mediated through metabolic pathways involved in carbohydrate, amino acid, and energy metabolisms.
CONCLUSIONS
Our results suggested that dietary intervention using the novel synbiotic can alleviate HFD-induced weight gain and restore gut microbial ecosystem homeostasis phylogenetically and functionally.
目的
肠道微生物群是影响代谢健康的重要因素。尽管益生菌、益生元和合生剂的饮食干预可以是调节肥胖和相关合并症的有效手段,但肠道微生物群落的潜在变化,特别是在功能水平上,尚未得到详细描述。在这项研究中,我们试图研究合生剂对调节肠道微生物群和减轻高脂肪饮食(HFD)诱导的小鼠代谢紊乱的影响。
方法
使用 10%(正常饮食,ND)或 60%(高脂肪饮食,HFD)总热量来自脂肪(猪油)的饮食喂养 SPF 雄性 C57BL/6J 小鼠。HFD 喂养小鼠的饮食干预包括(i)益生菌(动物双歧杆菌亚种。乳双歧杆菌和副干酪乳杆菌亚种。副干酪乳杆菌 DSM 46331),(ii)益生元(燕麦β-葡聚糖)和(iii)合生剂(i 和 ii 的混合物)治疗 12 周。除了详细描述宿主代谢参数外,还使用 16S rRNA 基因测序、代谢组学和靶向代谢组学分析等多组学方法系统地分析了微生物特征在系统发育和功能水平上的特征。
结果
合生剂干预显著降低了体重增加,并缓解了代谢并发症的特征。在系统发育水平上,合生剂治疗显著逆转了 HFD 诱导的微生物种群变化,无论是在丰富度还是特定分类群的相对丰度方面。鉴定出了可能介导合生剂有益作用的重要物种,如 Faecalibaculum rodentium 和 Alistipes putredinis。在功能水平上,短链脂肪酸和胆汁酸谱表明,所有饮食干预都显著恢复了盲肠中的乙酸盐、丙酸盐和丁酸盐水平,而合生剂处理最有效地降低了胆汁酸池。代谢组学表明,合生剂干预的作用可能通过涉及碳水化合物、氨基酸和能量代谢的代谢途径介导。
结论
我们的结果表明,使用新型合生剂的饮食干预可以缓解 HFD 诱导的体重增加,并在系统发育和功能上恢复肠道微生物生态系统的稳态。