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A post-weaning obesogenic diet exacerbates the detrimental effects of maternal obesity on offspring insulin signaling in adipose tissue

机译:断奶后吐露饮食加剧了母体肥胖对脂肪组织中的后代胰岛素信号传导的不利影响

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摘要

Previous studies have shown that maternal diet-induced obesity leads to increased risk of type 2 diabetes in offspring. The current study investigated if weaning onto an obesogenic diet exaggerated the detrimental effects of maternal diet-induced obesity in adipose tissue. Maternal obesity and offspring obesity led to reduced expression of key insulin signalling proteins, including insulin receptor substrate-1 (IRS-1). The effects of maternal obesity and offspring obesity were, generally, independent and additive. Irs1 mRNA levels were similar between all four groups of offspring, suggesting that in both cases post-transcriptional regulation was involved. Maternal diet-induced obesity increased miR-126 expression however levels of this miR were not influenced by a post-weaning obesogenic diet. In contrast, a post-weaning obesogenic diet was associated with increased levels of suppressor of cytokine signaling-1, implicating increased degradation of IRS-1 as an underlying mechanism. Our results suggest that whilst programmed reductions in IRS-1 are associated with increased levels of miR-126 and consequently reduced translation of Irs1 mRNA, the effects of a post-weaning obesogenic diet on IRS-1 are mediated by miR-126 independent mechanisms, including increased IRS-1 protein degradation. These divergent mechanisms explain why the combination of maternal obesity and offspring obesity leads to the most pronounced effects on offspring metabolism.
机译:以前的研究表明,母体饮食诱导的肥胖导致后代2型糖尿病的风险增加。如果对obesogenc饮食断奶夸大了母体饮食诱导的肥胖症在脂肪组织中的不利影响,则研究了目前的研究。产妇肥胖和后代肥胖导致关键胰岛素信号蛋白的表达减少,包括胰岛素受体基质-1(IRS-1)。母体肥胖和后代肥胖的影响通常是独立和添加剂。所有四组后代之间的IRS1 mRNA水平相似,表明在两种情况下涉及转录后调节。母体饮食诱导的肥胖增加miR-126表达,然而,这种mir的水平并不受断奶后溶血性饮食的影响。相比之下,断奶后溶血性饮食与细胞因子信号传导-1的抑制水平增加有关,暗示IRS-1的降解增加作为潜在机制。我们的研究结果表明,IRS-1中的编程减少与miR-126的水平增加以及IRS1 mRNA的翻译有关,因此IRS1 mRNA的翻译,次级后溶解饮食对IRS-1的影响是由MIR-126独立机制介导的,包括增加的IRS-1蛋白质降解。这些不同机制解释了为什么母体肥胖和后代肥胖的组合导致对后代新陈代谢的最明显的影响。

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