Department of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC, 3083, Australia.
Department of Physiology, The University of Melbourne, Parkville, VIC, 3010, Australia.
J Physiol. 2018 Dec;596(23):5947-5964. doi: 10.1113/JP275758. Epub 2018 Jul 26.
The placental insulin-like growth factor (IGF) system is critical for normal fetoplacental growth, which is dysregulated following several pregnancy perturbations including uteroplacental insufficiency and maternal obesity. We report that the IGF system was altered in placentae of mothers born growth restricted compared to normal birth weight mothers, with maternal diet- and fetal sex-specific responses. Additionally, we report increased body weight and plasma IGF1 concentrations in fetuses from chow-fed normal birth weight mothers that exercised prior to and continued during pregnancy compared to sedentary mothers. Exercise initiated during pregnancy, on the other hand, resulted in placental morphological alterations and increased IGF1 and IGF1R protein expression, which may in part be modulated by reduced Let 7f-1 miRNA abundance. Growth restriction of mothers before birth and exercise differentially regulate the placental IGF system with diet- and sex-specific responses, probably as a means to improve fetoplacental growth and development, and hence neonatal survival. This increased neonatal survival may prevent adult disease onset.
The insulin-like growth factor (IGF) system regulates fetoplacental growth and plays a role in disease programming. Dysregulation of the IGF system is implicated in several pregnancy perturbations associated with altered fetal growth, including intrauterine growth restriction and maternal obesity. Limited human studies have demonstrated that maternal exercise enhances fetoplacental growth and decreases cord IGF ligands, which may restore the placental IGF system in complicated pregnancies. This study investigated the impact maternal exercise has on the placental IGF system in placentae from mothers born growth restricted and if these outcomes are dependent on maternal diet or fetal sex. Uteroplacental insufficiency (Restricted) or sham (Control) surgery was induced on embryonic day (E) 18 in Wistar-Kyoto rats. F1 offspring were fed a chow or high-fat diet from weaning, and at 16 weeks were randomly allocated an exercise protocol: Sedentary, Exercised prior to and during pregnancy (Exercise), or Exercised during pregnancy only (PregEx). Females were mated (20 weeks) with placentae associated with F2 fetuses collected at E20. The placental IGF system mRNA abundance and placental morphology was altered in mothers born growth restricted. Exercise increased fetal weight and Control plasma IGF1 concentrations, and decreased female placental weight. PregEx did not influence fetoplacental growth but increased placental IGF1 and IGF1R (potentially modulated by reduced Let 7f-1 miRNA) and decreased placental IGF2 protein. Importantly, these placental IGF system changes occurred with sex-specific responses. These data highlight that exercise differently influences fetoplacental growth and the placental IGF system depending on maternal exercise initiation, which may prevent the transgenerational transmission of deficits and dysfunction.
胎盘胰岛素样生长因子(IGF)系统对于正常的胎-胎盘生长至关重要,而在多种妊娠干扰下,包括胎盘功能不全和母体肥胖,其会失调。我们报告称,与正常出生体重的母亲相比,出生时生长受限的母亲的胎盘 IGF 系统发生了改变,且存在母体饮食和胎儿性别特异性的反应。此外,我们还报告称,与久坐不动的母亲相比,在怀孕前和怀孕期间一直进行锻炼的正常出生体重母亲所生的胎儿体重和血浆 IGF1 浓度增加。相比之下,怀孕时开始运动导致胎盘形态发生改变,并增加了 IGF1 和 IGF1R 蛋白的表达,这可能部分受到 Let 7f-1 miRNA 丰度降低的调节。出生前母亲的生长受限和运动以饮食和性别特异性的方式对胎盘 IGF 系统进行了差异化调节,可能是改善胎-胎盘生长和发育以及新生儿存活率的一种手段。这种增加的新生儿存活率可能会防止成年疾病的发生。
胰岛素样生长因子(IGF)系统调节胎-胎盘生长,并在疾病编程中发挥作用。IGF 系统的失调与多种与胎儿生长改变相关的妊娠干扰有关,包括宫内生长受限和母体肥胖。有限的人体研究表明,母体运动可增强胎-胎盘生长,并降低脐带 IGF 配体,这可能恢复复杂妊娠中的胎盘 IGF 系统。本研究探讨了母体运动对出生时生长受限的母亲的胎盘 IGF 系统的影响,以及这些结果是否依赖于母体饮食或胎儿性别。在 Wistar-Kyoto 大鼠胚胎第 18 天(E)时诱导胎盘功能不全(受限)或假手术(对照)。F1 后代从断奶时开始分别喂食标准饮食或高脂肪饮食,在 16 周时随机分配进行运动方案:久坐不动、怀孕前和怀孕期间运动(运动)或仅在怀孕期间运动(妊娠运动)。20 周时,雌性与 F2 胎儿相关的胎盘交配,并在 E20 时收集胎盘。与对照组相比,出生时生长受限的母亲的胎盘 IGF 系统 mRNA 丰度和胎盘形态发生改变。运动增加了胎儿体重和对照组血浆 IGF1 浓度,并降低了雌性胎盘的重量。妊娠运动并没有影响胎-胎盘生长,但增加了胎盘 IGF1 和 IGF1R(可能通过减少 Let 7f-1 miRNA 进行调节),并降低了胎盘 IGF2 蛋白。重要的是,这些胎盘 IGF 系统的变化伴随着性别特异性的反应。这些数据表明,运动对胎-胎盘生长和胎盘 IGF 系统的影响取决于母体运动的开始,这可能防止代际传递缺陷和功能障碍。