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Effects of Gut Microbiota Manipulation by Antibiotics on Host Metabolism in Obese Humans: A Randomized Double-Blind Placebo-Controlled Trial

机译:抗生素操纵肠道菌群对肥胖人类宿主代谢的影响:随机双盲安慰剂对照试验

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摘要

The gut microbiota has been implicated in obesity and cardiometabolic diseases, although evidence in humans is scarce. We investigated how gut microbiota manipulation by antibiotics (7-day administration of amoxicillin, vancomycin, or placebo) affects host metabolism in 57 obese, prediabetic men. Vancomycin, but not amoxicillin, decreased bacterial diversity and reduced Firmicutes involved in short-chain fatty acid and bile acid metabolism, concomitant with altered plasma and/or fecal metabolite concentrations. Adipose tissue gene expression of oxidative pathways was upregulated by antibiotics, whereas immune-related pathways were downregulated by vancomycin. Antibiotics did not affect tissue-specific insulin sensitivity, energy/substrate metabolism, postprandial hormones and metabolites, systemic inflammation, gut permeability, and adipocyte size. Importantly, energy harvest, adipocyte size, and whole-body insulin sensitivity were not altered at 8-week follow-up, despite a still considerably altered microbial composition, indicating that interference with adult microbiota by 7-day antibiotic treatment has no clinically relevant impact on metabolic health in obese humans.
机译:肠道微生物群与肥胖和心脏代谢疾病有关,尽管人类的证据很少。我们调查了抗生素(7天服用阿莫西林,万古霉素或安慰剂)对肠道菌群的操纵如何影响57位肥胖的糖尿病前期男性的宿主代谢。万古霉素(而非阿莫西林)减少了细菌多样性,并减少了短链脂肪酸和胆汁酸代谢所涉及的Firmicutes,并伴有血浆和/或粪便代谢物浓度的改变。抗生素上调脂肪组织的氧化途径基因表达,而万古霉素则下调免疫相关途径。抗生素不影响组织特异性的胰岛素敏感性,能量/底物代谢,餐后激素和代谢产物,全身性炎症,肠通透性和脂肪细胞大小。重要的是,尽管微生物组成仍然有很大变化,但能量收集,脂肪细胞大小和全身胰岛素敏感性在8周随访中没有改变,这表明7天抗生素治疗对成人微生物群的干扰没有临床相关影响肥胖人类的代谢健康。

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