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Differential Effects of Exposure to Maternal Obesity or Maternal Weight Loss during the Periconceptional Period in the Sheep on Insulin Signalling Molecules in Skeletal Muscle of the Offspring at 4 Months of Age

机译:绵羊受孕期间母体肥胖或母体体重减轻对4个月大后代骨骼肌中胰岛素信号分子的差异影响

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摘要

Exposure to maternal obesity before and/or throughout pregnancy may increase the risk of obesity and insulin resistance in the offspring in childhood and adult life, therefore, resulting in its transmission into subsequent generations. We have previously shown that exposure to maternal obesity around the time of conception alone resulted in increased adiposity in female lambs. Changes in the abundance of insulin signalling molecules in skeletal muscle and adipose tissue precede the development of insulin resistance and type 2 diabetes. It is not clear, however, whether exposure to maternal obesity results in insulin resistance in her offspring as a consequence of the impact of increased adiposity on skeletal muscle or as a consequence of the programming of specific changes in the abundance of insulin signalling molecules in this tissue. We have used an embryo transfer model in the sheep to investigate the effects of exposure to either maternal obesity or to weight loss in normal and obese mothers preceding and for one week after conception on the expression and abundance of insulin signalling molecules in muscle in the offspring. We found that exposure to maternal obesity resulted in lower muscle GLUT-4 and Ser 9 phospho-GSK3α and higher muscle GSK3α abundance in lambs when compared to lambs conceived in normally nourished ewes. Exposure to maternal weight loss in normal or obese mothers, however, resulted in lower muscle IRS1, PI3K, p110β, aPKCζ, Thr 642 phospho-AS160 and GLUT-4 abundance in the offspring. In conclusion, maternal obesity or weight loss around conception have each programmed specific changes on subsets of molecules in the insulin signalling, glucose transport and glycogen synthesis pathways in offspring. There is a need for a stronger evidence base to ensure that weight loss regimes in obese women seeking to become pregnant minimize the metabolic costs for the next generation.
机译:在怀孕之前和/或整个怀孕期间暴露于母体肥胖症可能会增加儿童期和成年后代的肥胖症和胰岛素抵抗的风险,因此导致其传播给后代。我们以前的研究表明,仅在受孕时就暴露于母体肥胖会导致母羊的肥胖增加。骨骼肌和脂肪组织中胰岛素信号分子丰度的变化先于胰岛素抵抗和2型糖尿病的发生。然而,尚不清楚母体肥胖是否是由于肥胖增加对骨骼肌的影响或由于对胰岛素信号分子丰度的特定变化进行编程而导致其后代的胰岛素抵抗组织。我们在绵羊中使用了胚胎移植模型,研究了受孕前后正常妊娠和肥胖母亲暴露于母体肥胖或体重减轻对后代肌肉中胰岛素信号分子表达和丰度的影响。我们发现,与正常营养母羊中的羔羊相比,暴露于母体肥胖会导致羔羊较低的肌肉GLUT-4和Ser 9磷酸GSK3α以及较高的肌肉GSK3α丰度。然而,在正常或肥胖母亲中,孕妇的体重减轻会导致其后代肌肉IRS1,PI3K,p110β,aPKCζ,Thr 642磷酸化AS160和GLUT-4的丰度降低。总之,孕产期肥胖或体重减轻围绕后代中的胰岛素信号传导,葡萄糖转运和糖原合成途径中的分子子集都有特定的特定变化。需要有更强有力的证据基础,以确保寻求怀孕的肥胖女性的减肥方案将下一代的代谢成本降至最低。

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