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High-fat diet before and during pregnancy causes marked up-regulation of placental nutrient transport and fetal overgrowth in C57/BL6 mice

机译:怀孕前后高脂饮食会导致C57 / BL6小鼠胎盘营养运输和胎儿过度生长明显上调

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摘要

Maternal overweight and obesity in pregnancy often result in fetal overgrowth, which increases the risk for the baby to develop metabolic syndrome later in life. However, the mechanisms underlying fetal overgrowth are not established. We developed a mouse model and hypothesized that a maternal high-fat (HF) diet causes up-regulation of placental nutrient transport, resulting in fetal overgrowth. C57BL/6J female mice were fed a control (11% energy from fat) or HF (32% energy from fat) diet for 8 wk before mating and throughout gestation and were studied at embryonic day 18.5. The HF diet increased maternal adiposity, as assessed by fat pad weight, and circulating maternal leptin, decreased serum adiponectin concentrations, and caused a marked increase in fetal growth (+43%). The HF diet also increased transplacental transport of glucose (5-fold) and neutral amino acids (10-fold) in vivo. In microvillous plasma membranes (MVMs) isolated from placentas of HF-fed animals, protein expression of glucose transporter 1 (GLUT1) was increased 5-fold, and protein expression of sodium-coupled neutral amino acid transporter (SNAT) 2 was elevated 9-fold. In contrast, MVM protein expression of GLUT 3 or SNAT4 was unaltered. These data suggest that up-regulation of specific placental nutrient transporter isoforms constitute a mechanism linking maternal high-fat diet and obesity to fetal overgrowth.—Jones, H. N., Woollett, L. A., Barbour, N., Prasad, P. D., Powell, T. L., Jansson, T. High-fat diet before and during pregnancy causes marked up-regulation of placental nutrient transport and fetal overgrowth in C57/BL6 mice.
机译:孕妇的超重和肥胖通常会导致胎儿过度生长,从而增加婴儿在以后的生活中患代谢综合征的风险。但是,胎儿过度生长的机制尚未建立。我们开发了一种小鼠模型,并假设孕妇高脂(HF)饮食会导致胎盘营养运输的上调,从而导致胎儿过度生长。 C57BL / 6J雌性小鼠在交配前和整个妊娠过程中喂饲对照(11%能量的脂肪)或HF(32%能量的脂肪)饮食8周,在胚胎第18.5天进行研究。 HF饮食通过脂肪垫重量和循环的孕妇瘦素增加了孕妇的肥胖,降低了血清脂联素的浓度,并导致胎儿的生长显着增加(+ 43%)。 HF饮食在体内还增加了经胎盘葡萄糖(5倍)和中性氨基酸(10倍)的经胎盘运输。在从HF喂养动物的胎盘中分离出的微毛质膜(MVM)中,葡萄糖转运蛋白1(GLUT1)的蛋白质表达增加了5倍,而钠偶联中性氨基酸转运蛋白(SNAT)2的蛋白质表达则提高了9-折。相反,GLUT 3或SNAT4的MVM蛋白表达未改变。这些数据表明,特定胎盘营养转运蛋白同工型的上调构成了将孕产妇高脂饮食和肥胖与胎儿过度生长联系起来的机制。—Jones,HN,Woollett,LA,Barbour,N.,Prasad,PD,Powell,TL, Jansson,T.怀孕前和怀孕期间的高脂饮食会导致C57 / BL6小鼠胎盘营养运输和胎儿过度生长明显上调。

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