Hamilton M Kristina, Ronveaux Charlotte C, Rust Bret M, Newman John W, Hawley Melissa, Barile Daniela, Mills David A, Raybould Helen E
Department of Anatomy, Physiology, and Cell Biology, University of California Davis School of Veterinary Medicine, Davis, California.
Department of Nutrition, University of California Davis, Davis, California.
Am J Physiol Gastrointest Liver Physiol. 2017 May 1;312(5):G474-G487. doi: 10.1152/ajpgi.00427.2016. Epub 2017 Mar 9.
Microbial dysbiosis and increased intestinal permeability are targets for prevention or reversal of weight gain in high-fat (HF) diet-induced obesity (DIO). Prebiotic milk oligosaccharides (MO) have been shown to benefit the host intestine but have not been used in DIO. We hypothesized that supplementation with bovine MO would prevent the deleterious effect of HF diet on the gut microbiota and intestinal permeability and attenuate development of the obese phenotype. C57BL/6 mice were fed a control diet, HF (40% fat/kcal), or HF + prebiotic [6%/kg bovine milk oligosaccharides (BMO) or inulin] for 1, 3, or 6 wk. Gut microbiota and intestinal permeability were assessed in the ileum, cecum, and colon. Addition of BMO to the HF diet significantly attenuated weight gain, decreased adiposity, and decreased caloric intake; inulin supplementation also lowered weight gain and adiposity, but this did not reach significance. BMO and inulin completely abolished the HF diet-induced increase in paracellular and transcellular permeability in the small and large intestine. Both BMO and inulin increased abundance of beneficial microbes and in the ileum. However, inulin supplementation altered phylogenetic diversity and decreased species richness. We conclude that addition of BMO to the HF diet completely prevented increases in intestinal permeability and microbial dysbiosis and was partially effective to prevent weight gain in DIO. This study provides the first report of the effects of prebiotic bovine milk oligosaccharides on the host phenotype of high-fat diet-induced obesity in mice.
微生物群落失调和肠道通透性增加是预防或逆转高脂(HF)饮食诱导的肥胖(DIO)中体重增加的靶点。益生元低聚半乳糖(MO)已被证明对宿主肠道有益,但尚未用于DIO研究。我们假设补充牛源MO可以预防HF饮食对肠道微生物群和肠道通透性的有害影响,并减轻肥胖表型的发展。将C57BL/6小鼠分为三组,分别喂食对照饮食、HF(40%脂肪/千卡)或HF + 益生元饮食[6%/千克牛源低聚半乳糖(BMO)或菊粉],持续1、3或6周。对回肠、盲肠和结肠的肠道微生物群和肠道通透性进行评估。在HF饮食中添加BMO可显著减轻体重增加、降低肥胖程度并减少热量摄入;补充菊粉也能降低体重增加和肥胖程度,但未达到显著水平。BMO和菊粉完全消除了HF饮食诱导的小肠和大肠细胞旁及跨细胞通透性增加。BMO和菊粉均增加了回肠中有益微生物的丰度。然而,补充菊粉改变了系统发育多样性并降低了物种丰富度。我们得出结论,在HF饮食中添加BMO可完全预防肠道通透性增加和微生物群落失调,并在预防DIO体重增加方面部分有效。本研究首次报道了益生元牛源低聚半乳糖对小鼠高脂饮食诱导肥胖宿主表型的影响。