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Diet-induced changes in maternal gut microbiota and metabolomic profiles influence programming of offspring obesity risk in rats

机译:饮食诱导的母体肠道微生物和代谢物谱的变化影响大鼠后代肥胖风险的方案

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Maternal obesity and overnutrition during pregnancy and lactation can program an increased risk of obesity in offspring. In this context, improving maternal metabolism may help reduce the intergenerational transmission of obesity. Here we show that, in Sprague-Dawley rats, selectively altering obese maternal gut microbial composition with prebiotic treatment reduces maternal energy intake, decreases gestational weight gain, and prevents increased adiposity in dams and their offspring. Maternal serum metabolomics analysis, along with satiety hormone and gut microbiota analysis, identified maternal metabolic signatures that could be implicated in programming offspring obesity risk and highlighted the potential influence of maternal gut microbiota on maternal and offspring metabolism. In particular, the metabolomic signature of insulin resistance in obese rats normalized when dams consumed the prebiotic. In summary, prebiotic intake during pregnancy and lactation improves maternal metabolism in diet-induced obese rats in a manner that attenuates the detrimental nutritional programming of offspring associated with maternal obesity. Overall, these findings contribute to our understanding of the maternal mechanisms influencing the developmental programming of offspring obesity and provide compelling pre-clinical evidence for a potential strategy to improve maternal and offspring metabolic outcomes in human pregnancy.
机译:孕产妇肥胖和妊娠期哺乳期的过度,可以在后代计划增加肥胖风险。在这种情况下,改善孕产阶级的代谢可能有助于降低肥胖的代际传播。在这里,我们表明,在Sprague-Dawley大鼠中,选择性地改变具有益生元治疗的肥胖母体肠道微生物组合物可降低母体能量摄取,降低妊娠重量增益,并防止坝体中的肥厚增加和其后代增加。母体血清代谢组科分析,以及饱腹感染症和肠道微生物群分析,确定了母体代谢签名,可以涉及编程后代肥胖风险,并强调母体肠道微生物对母体和后代代谢的潜在影响。特别是,当坝消耗益生元时,肥胖大鼠胰岛素抗性的代谢组特征归一化。总之,怀孕期间的益生元摄入和哺乳期在饮食诱导的肥胖大鼠中提高了母体代谢,以抑制与母体肥胖相关的后代的不利营养规划。总体而言,这些调查结果有助于我们对影响后代肥胖发展方案的母体机制的理解,并为提高人类怀孕中的潜在战略提供引人注目的临床前证据,以提高人类怀孕中的孕产妇和后代代谢结果。

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