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Sex-specific association between the gut microbiome and high-fat diet-induced metabolic disorders in mice

机译:肠道微生物组和高脂饮食诱导的小鼠代谢障碍之间的性别特异性关联

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Accumulating evidence indicates that high-fat diet (HFD)-induced metabolic disorders are associated with dysbiosis of the gut microbiota. However, the sex-specific characteristics of the gut microbiota and its association with a sexually dimorphic response to a HFD remain unclear. Male and female mice were randomly assigned to receive a chow diet (CD) or HFD for 12 weeks. A group of HFD mice were pretreated with antibiotic cocktails for 4 weeks. Body weight, insulin sensitivity and the levels of serum metabolic parameters (blood glucose and insulin) were evaluated. 16S rRNA gene sequencing was performed to analyze the composition of the gut microbiota. HFD-induced body weight gain (BWG) was higher in male mice than in female mice. While insulin resistance was increased in the HFD group compared to CD group in male mice, there was no difference in insulin resistance among female mice. Antibiotic-pretreatment alleviated HFD-induced insulin resistance in male mice and elevated fasting blood glucose in female mice. The composition of the gut microbiota in male mice was remarkably different from that in female mice independent of diet. A higher abundance of the genera Parabacteroides, Lactobacillus, Bacteroides, and Bifidobacterium was observed in females than inmales. HFD feeding also influenced the structure of the gut microbiota, as it decreased the abundance of short-chain fatty acids-producing bacteria including Roseburia and Lachnospiraceae_NK4A136_group. Alterations in the gut microbiota in response to antibiotics followed by HFD were different between males and females, indicating sex-dependent sensitivity to antibiotics. We identified that sex had a greater impact on the composition of gut microbiota than environmental factors (HFD and antibiotics). The enrichment of beneficial microbes in female mice may be associated with the resistance of female mice to HFD-induced metabolic disorders, which was weakened by antibiotic pretreatment.
机译:累积证据表明高脂饮食(HFD)诱导的代谢障碍与肠道微生物瘤的脱敏相关有关。然而,肠道微生物群的性别特异性特征及其与对HFD的性二甲响应的关联仍然不清楚。随机分配雄性和雌性小鼠以接受12周的食物饮食(CD)或HFD。将一组HFD小鼠用抗生素鸡尾酒预处理4周。评估体重,胰岛素敏感性和血清代谢参数(血糖和胰岛素)的水平。进行16S rRNA基因测序以分析肠道微生物菌的组成。 HFD诱导的体重增加(BWG)在雄性小鼠中比女性小鼠更高。在HFD组中增加胰岛素抵抗与雄性小鼠的CD组相比,雌性小鼠之间的胰岛素抗性没有差异。抗生素预处理缓解了雄性小鼠中的HFD诱导的胰岛素抗性,在雌性小鼠中升高的血葡萄糖。在雄性小鼠中肠道微生物的组成显着与饮食无关的女性小鼠中的显着不同。在女性中观察到较高丰富的属ParaMacteroides,乳酸杆菌,诱导和双歧杆菌,而不是Inmales。 HFD饲养也影响了肠道微生物群的结构,因为它降低了在包括Roseburia和Lachnospireae_nk4a136_group的生产细菌的丰富的短链脂肪酸细菌。肠道微生物群的改变响应抗生素,然后患有HFD在雄性和雌性之间是不同的,表明对抗生素的性爱依赖性敏感性。我们发现性别对肠道微生物群组成的影响而不是环境因素(HFD和抗生素)。雌性小鼠有益微生物的富集可能与雌性小鼠的抗性与HFD诱导的代谢紊乱有关,这通过抗生素预处理削弱。

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