Department of Biochemistry and Biomedical Sciences, Farncombe Family Digestive Health Research Institute McMaster University, Hamilton, L8N 3Z5, ON, Canada.
Departments of Genetics and Medicine, Stanford University, Stanford, 94305, California, USA.
Nat Commun. 2018 Nov 8;9(1):4681. doi: 10.1038/s41467-018-07146-5.
The intestinal microbiota and insulin sensitivity are rapidly altered after ingestion of obesogenic diets. We find that changes in the composition of the fecal microbiota precede changes in glucose tolerance when mice are fed obesogenic, low fiber, high fat diets (HFDs). Antibiotics alter glycemia during the first week of certain HFDs, but antibiotics show a more robust improvement in glycemic control in mice with protracted obesity caused by long-term feeding of multiple HFDs. Microbiota transmissible dysglycemia and glucose intolerance only occur when germ-free mice are exposed to obesity-related microbes for more than 45 days. We find that sufficient host exposure time to microbiota derived from HFD-fed mice allows microbial factors to contribute to insulin resistance, independently from increased adiposity in mice. Our results are consistent with intestinal microbiota contributing to chronic insulin resistance and dysglycemia during prolonged obesity, despite rapid diet-induced changes in the taxonomic composition of the fecal microbiota.
肠道微生物群和胰岛素敏感性在摄入致肥胖饮食后会迅速发生改变。我们发现,当小鼠摄入致肥胖、低纤维、高脂肪饮食(HFD)时,粪便微生物群的组成变化先于葡萄糖耐量变化。抗生素会在某些 HFD 的第一周改变血糖水平,但抗生素在由长期喂食多种 HFD 引起的肥胖持续存在的小鼠中显示出更显著的血糖控制改善。只有当无菌小鼠暴露于与肥胖相关的微生物超过 45 天时,才会发生可传播的糖代谢紊乱和葡萄糖不耐受。我们发现,宿主有足够的时间接触来自 HFD 喂养小鼠的微生物群,使微生物因素能够导致胰岛素抵抗,而与小鼠的肥胖程度增加无关。尽管粪便微生物群的分类组成因饮食而迅速发生变化,但我们的结果表明,肠道微生物群在肥胖持续期间有助于慢性胰岛素抵抗和糖代谢紊乱。