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Structural modulation of the gut microbiota and the relationship with body weight: compared evaluation of liraglutide and saxagliptin treatment

机译:肠道微生物的结构调节及与体重关系的关系:枸杞子和沙克宫素治疗的比较评价

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The mechanisms underlying the weight-loss effect of GLP-1 receptor agonists need further elucidation. The present study was performed to explore the effects of liraglutide and saxagliptin on the composition of the gut microbiota. Mice were randomly treated with saxagliptin or liraglutide for eight weeks. Their metabolic profiles were assessed, and 454 pyrosequencing of 16s rRNA of faeces was performed. Liraglutide induced a smaller body weight gain in mice. The pyrosequencing showed that liraglutide, but not saxagliptin, substantially changed the overall structure of the gut microbiota as well as the relative abundance of weight-relevant phylotypes. Subsequent ridge regression analyses indicated that, in addition to food intake (β?=?-0.182, p?=?0.043 in phylotypes inversely correlated with body weight) and blood glucose level (β?=?-0.240, p?=?0.039 in phylotypes positively correlated with body weight), the administration of liraglutide was another independent factor associated with the abundance of weight-relevant phylotypes (β?=?0.389, p?=?6.24e-5 in inversely correlated ones; β?=?-0.508, p?=?2.25e-5 in positively correlated ones). These results evidenced that GLP-1 receptor agonist liraglutide could modulate the composition of the gut microbiota, leading to a more lean-related profile that was consistent with its weight-losing effect.
机译:GLP-1受体激动剂的减肥效应的机制需要进一步阐明。进行本研究探讨了丽菌胺和Saxagliptin对肠道微生物组成的影响。用Saxagliptin或Liraglutide随机处理小鼠八周。评估它们的代谢型材,并进行了454次粪便粪便的焦点。 Liraglutide在小鼠中诱导较小的体重增加。焦塞术显示紫胶蛋白,但不是西撒颌骨,基本上改变了肠道微生物的整体结构以及相对丰富的体重相关的植物。随后的脊回归分析表明,除了食物摄入量(β?=Δ - 0.182,p?=Δ= 0.043,与体重相反)和血糖水平(β?=? - 0.240,p?= 0.039在阳性与体重呈阳性相关)中,Liraglutide的给药是与富含体重相关的(βα= 0.389,P≥6.24E-5的丰度相关的另一个独立因子,其成反比地相关;β=? -0.508,p?=?2.25e-5在正相关的中)。这些结果证明了GLP-1受体激动剂丽耳蛋白质可以调节肠道微生物群的组成,导致更瘦性的曲线与其重量效应一致。

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