Kiilerich Pia, Myrmel Lene Secher, Fjære Even, Hao Qin, Hugenholtz Floor, Sonne Si Brask, Derrien Muriel, Pedersen Lone Møller, Petersen Rasmus Koefoed, Mortensen Alicja, Licht Tine Rask, Rømer Maria Unni, Vogel Ulla Birgitte, Waagbø Linn Jeanette, Giallourou Natasa, Feng Qiang, Xiao Liang, Liu Chuan, Liaset Bjørn, Kleerebezem Michiel, Wang Jun, Madsen Lise, Kristiansen Karsten
Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, Copenhagen, Denmark;
Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, Copenhagen, Denmark; National Institute of Nutrition and Seafood Research, Bergen, Norway;
Am J Physiol Endocrinol Metab. 2016 Jun 1;310(11):E886-99. doi: 10.1152/ajpendo.00363.2015. Epub 2016 Mar 29.
Female C57BL/6J mice were fed a regular low-fat diet or high-fat diets combined with either high or low protein-to-sucrose ratios during their entire lifespan to examine the long-term effects on obesity development, gut microbiota, and survival. Intake of a high-fat diet with a low protein/sucrose ratio precipitated obesity and reduced survival relative to mice fed a low-fat diet. By contrast, intake of a high-fat diet with a high protein/sucrose ratio attenuated lifelong weight gain and adipose tissue expansion, and survival was not significantly altered relative to low-fat-fed mice. Our findings support the notion that reduced survival in response to high-fat/high-sucrose feeding is linked to obesity development. Digital gene expression analyses, further validated by qPCR, demonstrated that the protein/sucrose ratio modulated global gene expression over time in liver and adipose tissue, affecting pathways related to metabolism and inflammation. Analysis of fecal bacterial DNA using the Mouse Intestinal Tract Chip revealed significant changes in the composition of the gut microbiota in relation to host age and dietary fat content, but not the protein/sucrose ratio. Accordingly, dietary fat rather than the protein/sucrose ratio or adiposity is a major driver shaping the gut microbiota, whereas the effect of a high-fat diet on survival is dependent on the protein/sucrose ratio.
雌性C57BL/6J小鼠在其整个生命周期内被喂食常规低脂饮食或高蛋白/蔗糖比或低蛋白/蔗糖比的高脂饮食,以研究其对肥胖发展、肠道微生物群和存活率的长期影响。与喂食低脂饮食的小鼠相比,摄入低蛋白/蔗糖比的高脂饮食会导致肥胖并降低存活率。相比之下,摄入高蛋白/蔗糖比的高脂饮食可减轻终生体重增加和脂肪组织扩张,与喂食低脂饮食的小鼠相比,存活率没有显著改变。我们的研究结果支持这样一种观点,即高脂/高蔗糖喂养导致的存活率降低与肥胖发展有关。通过qPCR进一步验证的数字基因表达分析表明,蛋白/蔗糖比随时间调节肝脏和脂肪组织中的全局基因表达,影响与代谢和炎症相关的途径。使用小鼠肠道芯片分析粪便细菌DNA发现,肠道微生物群的组成与宿主年龄和饮食脂肪含量有关,但与蛋白/蔗糖比无关。因此,饮食脂肪而非蛋白/蔗糖比或肥胖是塑造肠道微生物群的主要驱动因素,而高脂饮食对存活率的影响取决于蛋白/蔗糖比。