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Maternal Obesity and Western-Style Diet Impair Fetal and Juvenile Offspring Skeletal Muscle Insulin-Stimulated Glucose Transport in Nonhuman Primates

机译:产妇肥胖和西式饮食患有胎儿和少年后代骨骼肌刺激葡萄糖运输在非人的灵长类动物

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摘要

Infants born to mothers with obesity have a greater risk for childhood obesity and metabolic diseases; however, the underlying biological mechanisms remain poorly understood. We used a Japanese macaque model to investigate whether maternal obesity combined with a Western-style diet (WSD) impairs offspring muscle insulin action. Adult females were fed a control or WSD prior to and during pregnancy through lactation, and offspring subsequently weaned to a control or WSD. Muscle glucose uptake and signaling were measured ex vivo in fetal (n = 5–8/group) and juvenile (n = 8/group) offspring. In vivo signaling was evaluated after an insulin bolus just prior to weaning (n = 4–5/group). Maternal WSD reduced insulin-stimulated glucose uptake and impaired insulin signaling at the level of Akt phosphorylation in fetal muscle. In juvenile offspring, insulin-stimulated glucose uptake was similarly reduced by both maternal and postweaning WSD and corresponded to modest reductions in insulin-stimulated Akt phosphorylation relative to controls. We conclude that maternal WSD leads to a persistent decrease in offspring muscle insulin-stimulated glucose uptake even in the absence of increased offspring adiposity or markers of systemic insulin resistance. Switching offspring to a healthy diet did not reverse the effects of maternal WSD on muscle insulin action, suggesting earlier interventions may be warranted.
机译:患有肥胖的母亲出生的婴儿对儿童肥胖和代谢疾病具有更大的风险;然而,潜在的生物机制仍然明白很差。我们使用了日本猕猴模型来研究母体肥胖是否与西式饮食(WSD)损害后代肌肉胰岛素作用。通过哺乳期之前和怀孕期间,在怀孕期间和WSD喂食成年女性,后代随后断奶给控制或WSD。测量胎儿葡萄糖摄取和信号传导,胎儿(n = 5-8 /组)和少年(n = 8 /组)后代。在发生断奶之前在胰岛素推注后评估体内信号传导(n = 4-5 /组)。母体WSD降低胰岛素刺激的葡萄糖摄取和胎儿肌肉中Akt磷酸化水平的胰岛素信号传导受损。在少年后代,母体和后两种WSD类似地减少了胰岛素刺激的葡萄糖摄取,并且相对于对照对应于胰岛素刺激的AKT磷酸化的适度降低。我们得出结论,即使在没有增加的后代肥胖或全身胰岛素抵抗的标记的情况下,母体WSD也导致后代肌肉胰岛素刺激的葡萄糖摄取的持续减少。将后代切换到健康饮食并未逆转母体WSD对肌肉胰岛素作用的影响,提出了早期的干预措施。

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