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膳食脂肪和肠道微生物群的相互作用决定了小鼠的饮食诱导肥胖。

Dietary fat and gut microbiota interactions determine diet-induced obesity in mice.

机构信息

ZIEL - Institute for Food and Health, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany; Chair of Molecular Nutritional Medicine, Technical University of Munich, TUM School of Life Sciences Weihenstephan, EKFZ - Else Kröner-Fresenius-Center for Nutritional Medicine, Gregor-Mendel-Str. 2, 85354 Freising, Germany.

Research Unit Analytical BioGeoChemistry, Department of Environmental Sciences, Helmholtz Zentrum München, Ingolstädter Landstr.1, 85764 Neuherberg, Germany.

出版信息

Mol Metab. 2016 Oct 13;5(12):1162-1174. doi: 10.1016/j.molmet.2016.10.001. eCollection 2016 Dec.

Abstract

OBJECTIVE

Gut microbiota may promote positive energy balance; however, germfree mice can be either resistant or susceptible to diet-induced obesity (DIO) depending on the type of dietary intervention. We here sought to identify the dietary constituents that determine the susceptibility to body fat accretion in germfree (GF) mice.

METHODS

GF and specific pathogen free (SPF) male C57BL/6N mice were fed high-fat diets either based on lard or palm oil for 4 wks. Mice were metabolically characterized at the end of the feeding trial. FT-ICR-MS and UPLC-TOF-MS were used for cecal as well as hepatic metabolite profiling and cecal bile acids quantification, respectively. Hepatic gene expression was examined by qRT-PCR and cecal gut microbiota of SPF mice was analyzed by high-throughput 16S rRNA gene sequencing.

RESULTS

GF mice, but not SPF mice, were completely DIO resistant when fed a cholesterol-rich lard-based high-fat diet, whereas on a cholesterol-free palm oil-based high-fat diet, DIO was independent of gut microbiota. In GF lard-fed mice, DIO resistance was conveyed by increased energy expenditure, preferential carbohydrate oxidation, and increased fecal fat and energy excretion. Cecal metabolite profiling revealed a shift in bile acid and steroid metabolites in these lean mice, with a significant rise in 17β-estradiol, which is known to stimulate energy expenditure and interfere with bile acid metabolism. Decreased cecal bile acid levels were associated with decreased hepatic expression of genes involved in bile acid synthesis. These metabolic adaptations were largely attenuated in GF mice fed the palm-oil based high-fat diet. We propose that an interaction of gut microbiota and cholesterol metabolism is essential for fat accretion in normal SPF mice fed cholesterol-rich lard as the main dietary fat source. This is supported by a positive correlation between bile acid levels and specific bacteria of the order (phylum ) as a characteristic feature of normal SPF mice fed lard.

CONCLUSIONS

In conclusion, our study identified dietary cholesterol as a candidate ingredient affecting the crosstalk between gut microbiota and host metabolism.

摘要

目的

肠道微生物群可能促进积极的能量平衡;然而,根据饮食干预的类型,无菌(GF)小鼠可能对饮食诱导的肥胖(DIO)具有抗性或易感性。我们在此旨在确定决定无菌(GF)小鼠体脂肪积累易感性的饮食成分。

方法

雄性 C57BL/6N GF 和特定病原体自由(SPF)小鼠分别用猪油或棕榈油基高脂肪饮食喂养 4 周。在喂养试验结束时对小鼠进行代谢特征分析。FT-ICR-MS 和 UPLC-TOF-MS 分别用于回肠和肝脏代谢产物谱分析以及回肠胆汁酸定量。通过 qRT-PCR 检查肝基因表达,通过高通量 16S rRNA 基因测序分析 SPF 小鼠的回肠肠道微生物群。

结果

当喂食富含胆固醇的猪油基高脂肪饮食时,GF 小鼠完全抵抗 DIO,而喂食不含胆固醇的棕榈油基高脂肪饮食时,DIO 与肠道微生物群无关。在 GF 猪油喂养的小鼠中,DIO 抗性是通过增加能量消耗、优先碳水化合物氧化以及增加粪便脂肪和能量排泄来传递的。这些瘦小鼠的回肠代谢产物谱显示胆汁酸和类固醇代谢物发生了转变,17β-雌二醇显着升高,已知其可刺激能量消耗并干扰胆汁酸代谢。回肠胆汁酸水平降低与参与胆汁酸合成的基因在肝脏中的表达降低有关。这些代谢适应在 GF 小鼠喂食棕榈油基高脂肪饮食时大大减弱。我们提出,肠道微生物群和胆固醇代谢之间的相互作用对于正常 SPF 小鼠在以富含胆固醇的猪油作为主要饮食脂肪来源时的脂肪积累是必不可少的。这得到了一个积极的支持相关性在胆汁酸水平和作为正常 SPF 小鼠喂食猪油的特征特征的顺序(门)的特定细菌之间。

结论

总之,我们的研究确定了饮食胆固醇作为影响肠道微生物群和宿主代谢之间串扰的候选成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7d6/5123202/5415d79515cd/figs1.jpg

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