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Ketogenic Diets Induced Glucose Intolerance and Lipid Accumulation in Mice with Alterations in Gut Microbiota and Metabolites

机译:酮味饮食在小鼠中诱导葡萄糖不耐受和脂质积累,随着肠道微生物和代谢物的改变

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The ketogenic diet with extremely high fat and very low carbohydrate levels is very popular in society today. Although it has beneficial effects on epilepsy and neurodegenerative diseases, how ketogenic diets impact host glucose and lipid metabolism and gut microbiota still needs further investigation. ABSTRACT The ketogenic diet (KD), which can induce changes in gut microbiota, has shown benefits for epilepsy and several neurodegenerative diseases. However, the effects of a KD on glucose and lipid metabolism remain inconclusive. Using two formulas of ketogenic diets (KDR with 89.5% fat and KDH with 91.3% fat), which are commonly used in mouse trials, we found that KDR but not KDH induced insulin resistance and damaged glucose homeostasis, while KDH induced more fat accumulation in mice. Further study showed that KD impacted glucose metabolism, which was related to the sources of fat, while both the sources and proportions of fat affected lipid metabolism. And the KD widely used in human studies still induced insulin resistance and fat accumulation in mice. Moreover, KDs changed the gut microbiota and metabolites in mice, and the sources and proportions of fat in the diets respectively changed the abundance of specific bacteria and metabolites which were correlated with parameters related to glucose intolerance and lipid accumulation. Overall, our study demonstrated that the metabolic disorders induced by KDs are closely related to the source and proportion of fat in the diet, which may be associated with the changes of the gut microbiota and metabolites.
机译:当今甲基水溶性极高脂肪和非常低的碳水化合物水平的酮饮食非常受欢迎。虽然它对癫痫和神经退行性疾病具有有益的影响,但酮饮食如何影响宿主葡萄糖和脂质代谢以及肠道微生物仍需要进一步调查。摘要酮饮食(KD),可诱导肠道微生物群的变化,表明了癫痫和几种神经变性疾病的益处。然而,KD对葡萄糖和脂质代谢的影响仍然不确定。使用两种酮饮食(KDR含有89.5%脂肪和91.3%脂肪)的公式,这些饮食通常用于小鼠试验中,我们发现KDR但不是KDH诱导胰岛素抵抗和受损的葡萄糖稳态,而KDH诱导脂肪积累更多老鼠。进一步的研究表明,KD受到葡萄糖代谢的影响,这与脂肪来源有关,而脂肪的来源和比例影响脂质代谢。广泛用于人类研究的KD仍然诱导小鼠胰岛素抵抗和脂肪积累。此外,KDS改变了小鼠的肠道微生物群和代谢物,饮食中脂肪的来源和脂肪的比例分别改变了与葡萄糖不耐受和脂质积累相关的参数相关的特定细菌和代谢物的丰富。总体而言,我们的研究表明,KDS诱导的代谢紊乱与饮食中脂肪的源和比例密切相关,这可能与肠道微生物和代谢物的变化有关。

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