Late-gestation maternal undernutrition induces circulatory redistribution while preserving uteroplacental function independent of fetal glycaemic state

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Steven K.S. Cho, Jack R.T. Darby, Brahmdeep S. Saini, Stacey L. Holman, Mitchell C. Lock, Sunthara Rajan Perumal, Georgia K. Williams, Christopher K. Macgowan, Mike Seed, Janna L. Morrison
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引用次数: 0

Abstract

Programming effects of maternal undernutrition on fetal metabolic and cardiovascular systems are well elucidated, yet a detailed characterization of maternal haemodynamics is not available. This study used comprehensive cardiovascular magnetic resonance (CMR) imaging to quantify maternal haemodynamics after 29 days (111–140 days) of late-gestation undernutrition (LGUN) in pregnant sheep. Control ewes received 100% of metabolizable energy requirements (MERs, n = 15), whereas LGUN ewes were globally nutrient restricted to 50% MER (n = 18), with a subset of fetuses undergoing continuous glucose infusion (LGUN + G, n = 6/18). Ewes underwent CMR (138–140 days’ gestation), and placental tissue was collected the next day. Ewes in both LGUN groups had reduced body weight and mean blood glucose concentration across gestation. Ventricular dimensions were lower in both LGUN groups. Uterine artery blood flow (QUtA) was elevated in the LGUN group compared with controls, whereas peripheral blood flow was reduced and further diminished in LGUN + G. Maternal weight change correlated with all haemodynamic parameters across all groups. Uteroplacental oxygen and glucose delivery were increased in LGUN compared to control ewes, whereas uteroplacental oxygen consumption was preserved. LGUN did not impact placental or fetal weight, and markers of brain-sparing physiology were absent. Placental expression of insulin-like growth factors (IGF-1 and IGF-2) and their receptors, glucose, fatty acid (FA) or amino acid transporters and markers of angiogenesis was not impacted. FA transporter expression was positively correlated with QUtA, and FA binding protein correlated negatively with maternal weight change. Maternal cardiovascular adaptations in response to LGUN manifest as preservation of placental growth and function, thereby preserving fetal growth.

Key points

  • Maternal undernutrition during pregnancy alters fetal metabolic and cardiovascular physiology, but little is known about alterations in maternal haemodynamics.
  • Late-gestation undernutrition (LGUN) and LGUN + G redirected maternal blood flow from the periphery to the uteroplacental unit, concomitantly increasing the delivery of glucose and oxygen to the uteroplacental unit.
  • Substrate transporter expression and uteroplacental oxygen consumption were preserved in LGUN and LGUN + G, suggesting prioritization of the placenta.
  • This study is the first to report detailed maternal haemodynamics in the setting of maternal undernutrition, where placental growth and function were maintained, ultimately preserving fetal oxygen metabolism and growth.

Abstract Image

妊娠晚期母体营养不良可诱导循环再分布,同时保持子宫胎盘功能,与胎儿血糖状态无关。
母体营养不良对胎儿新陈代谢和心血管系统的编程影响已被充分阐明,但母体血流动力学的详细描述尚不存在。本研究利用全面的心血管磁共振(CMR)成像技术,对孕羊妊娠晚期营养不良(LGUN)29天(111-140天)后的母体血液动力学进行量化。对照组母羊摄入 100%的可代谢能量需要量(MERs,n = 15),而 LGUN 母羊的总体营养限制为 50% MER(n = 18),其中一部分胎儿接受持续葡萄糖输注(LGUN + G,n = 6/18)。母羊接受 CMR(妊娠 138-140 天),并在第二天采集胎盘组织。LGUN 两组母羊的体重和平均血糖浓度在整个妊娠期都有所下降。两组 LGUN 母羊的心室尺寸均较低。与对照组相比,LGUN 组的子宫动脉血流(QUtA)升高,而外周血流降低,LGUN + G 组的外周血流进一步降低。与对照组相比,LGUN 组母羊的子宫胎盘氧气和葡萄糖输送量增加,而子宫胎盘耗氧量保持不变。LGUN 不影响胎盘或胎儿的体重,也不存在保脑生理指标。胰岛素样生长因子(IGF-1和IGF-2)及其受体、葡萄糖、脂肪酸(FA)或氨基酸转运体以及血管生成标记物的胎盘表达未受影响。脂肪酸转运体的表达与 QUtA 呈正相关,而脂肪酸结合蛋白与母体体重变化呈负相关。母体心血管对 LGUN 的适应表现为胎盘生长和功能的保护,从而保护胎儿的生长。要点:孕期母体营养不良会改变胎儿的代谢和心血管生理,但对母体血流动力学的改变却知之甚少。妊娠晚期营养不良(LGUN)和 LGUN + G 使母体血流从外周转向子宫胎盘,同时增加了向子宫胎盘输送葡萄糖和氧气。在 LGUN 和 LGUN + G 中,底物转运体的表达和子宫胎盘的耗氧量保持不变,这表明胎盘有优先权。这项研究首次详细报告了在母体营养不良的情况下,胎盘的生长和功能得以维持,最终保护了胎儿的氧代谢和生长。
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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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