Department of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC, 3083, Australia; Department of Physiology, The University of Melbourne, Parkville, VIC, 3010, Australia.
Department of Physiology, The University of Melbourne, Parkville, VIC, 3010, Australia.
Placenta. 2018 Dec 15;74:47-54. doi: 10.1016/j.placenta.2018.12.005.
Fetal growth and development are dependent on adequate placental nutrient transfer. The surface area of the placental villous network is a key determinant of nutrient exchange, which is regulated by vasculogenic and angiogenic factors. These factors are altered by intrauterine growth restriction (IUGR) and maternal obesity in both the first (F1) and second (F2) generations. We investigated the impact of endurance exercise in IUGR dams fed a High-fat diet on placental vasculogenesis and angiogenesis. 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 further allocated an exercise protocol; Sedentary, Exercised prior to and during pregnancy (Exercise), or Exercised during pregnancy only (PregEx). Females were mated (20 weeks) and F2 placentae collected at E20. Maternal Restriction, High-fat feeding and Exercise had a minimal impact on placental regulators of vasculogenesis and angiogenesis. However, Restriction increased placental labyrinth tissue area in Chow-fed dams. PregEx induced overt adaptations, including increased VEGFA and decreased PLGF protein expression, and reduced blood space area. These alterations were sex-dependent and associated with alterations in miRNA27a, a known regulator of VEGF translation. These data highlight that maternal exercise initiated during pregnancy (PregEx) causes alterations in placental vasculogenesis and angiogenesis in a sex-dependent manner, with minimal Restriction and maternal diet effects. However, further investigation is required to determine if these adaptations are beneficial or harmful for maternal and fetoplacental outcomes.
胎儿的生长和发育依赖于胎盘充足的营养转移。胎盘绒毛网络的表面积是营养交换的关键决定因素,由血管生成和血管生成因子调节。这些因子在宫内生长受限(IUGR)和母体肥胖的第一(F1)和第二(F2)代中都会发生改变。我们研究了在高脂饮食喂养的 IUGR 母鼠中进行耐力运动对胎盘血管生成和血管生成的影响。在 Wistar-Kyoto 大鼠的胚胎第 18 天(E)进行子宫胎盘功能不全(受限)或假手术(对照)。F1 后代从断奶开始分别喂食普通饮食或高脂饮食,16 周时进一步分配运动方案;久坐、妊娠前和妊娠期间运动(运动)或仅妊娠期间运动(PregEx)。雌性大鼠交配(20 周),在 E20 时收集 F2 胎盘。母体限制、高脂喂养和运动对血管生成和血管生成的胎盘调节作用影响不大。然而,在喂食普通饮食的母鼠中,限制增加了胎盘迷路组织面积。PregEx 诱导了明显的适应,包括 VEGFA 蛋白表达增加和 PLGF 蛋白表达减少,以及血液空间面积减少。这些改变是性别依赖的,并与 miRNA27a 的改变有关,miRNA27a 是 VEGF 翻译的已知调节因子。这些数据表明,在妊娠期间开始的母体运动(PregEx)以性别依赖的方式引起胎盘血管生成和血管生成的改变,而母体限制和饮食的影响较小。然而,需要进一步的研究来确定这些适应是否对母体和胎儿胎盘结局有益或有害。