Early Origins of Adult Health Research Group, School of Pharmacy & Medical Sciences, Sansom Institute for Health Research, University of South Australia, Adelaide, SA, 5001, Australia.
J Physiol. 2018 Jun;596(12):2345-2358. doi: 10.1113/JP275806. Epub 2018 May 20.
This study investigates the impact of decreased fetal plasma glucose concentrations on the developing heart in late gestation, by subjecting pregnant ewes to a 50% global nutrient restriction. Late gestation undernutrition (LGUN) decreased fetal plasma glucose concentrations whilst maintaining a normoxemic blood gas status. LGUN increased the mRNA expression of IGF2 and IGF2R. Fetal plasma glucose concentrations, but not fetal blood pressure, were significantly correlated with IGF2 expression and the activation of CAMKII in the fetal right ventricle. LGUN increased interstitial collagen deposition and altered the protein abundance of phospho-PLB and phospho-troponin I, regulators of cardiac contractility and relaxation. This study shows that a decrease in fetal plasma glucose concentrations may play a role in the development of detrimental changes in the right ventricle in early life, highlighting CAMKII as a potential target for the development of intervention strategies.
Exposure of the fetus to a range of environmental stressors, including maternal undernutrition, is associated with an increased risk of death from cardiovascular disease in adult life. This study aimed to determine the effect of maternal nutrient restriction in late gestation on the molecular mechanisms that regulate cardiac growth and development of the fetal heart. Maternal undernutrition resulted in a decrease in fetal glucose concentrations across late gestation, whilst fetal arterial PO2 remained unchanged between the control and late gestation undernutrition (LGUN) groups. There was evidence of an up-regulation of IGF2/IGF2R signalling through the CAMKII pathway in the fetal right ventricle in the LGUN group, suggesting an increase in hypertrophic signalling. LGUN also resulted in an increased mRNA expression of COL1A, TIMP1 and TIMP3 in the right ventricle of the fetal heart. In addition, there was an inverse relationship between fetal glucose concentrations and COL1A expression. The presence of interstitial fibrosis in the heart of the LGUN group was confirmed through the quantification of picrosirius red-stained sections of the right ventricle. We have therefore shown that maternal undernutrition in late gestation may drive the onset of myocardial remodelling in the fetal right ventricle and thus has negative implications for right ventricle function and cardiac health in later life.
本研究通过对怀孕母羊进行 50%的全球营养限制,研究了胎盘中葡萄糖浓度降低对晚期妊娠中发育中心脏的影响。晚期妊娠营养不良(LGUN)降低了胎儿血浆葡萄糖浓度,同时保持正常的血氧血液气体状态。LGUN 增加了 IGF2 和 IGF2R 的 mRNA 表达。胎儿血浆葡萄糖浓度,但不是胎儿血压,与胎儿右心室中 IGF2 的表达和 CAMKII 的激活呈显著相关。LGUN 增加了间质胶原沉积,并改变了 PLB 和 troponin I 的磷酸化蛋白丰度,这是心脏收缩和舒张的调节因子。本研究表明,胎儿血浆葡萄糖浓度的降低可能在生命早期右心室发育不良变化的发展中起作用,突出了 CAMKII 作为干预策略发展的潜在靶点。
胎儿暴露于一系列环境应激源,包括母体营养不良,与成年期心血管疾病死亡风险增加有关。本研究旨在确定妊娠晚期母体营养限制对调节胎儿心脏生长和发育的分子机制的影响。母体营养不良导致整个晚期妊娠胎儿葡萄糖浓度降低,而胎儿动脉 PO2 在对照组和晚期妊娠营养不良(LGUN)组之间保持不变。LGUN 组胎儿右心室中 IGF2/IGF2R 信号通过 CAMKII 途径的上调表明,肥大信号增加。LGUN 还导致胎儿心脏右心室中 COL1A、TIMP1 和 TIMP3 的 mRNA 表达增加。此外,胎儿葡萄糖浓度与 COL1A 表达呈负相关。通过对右心室 picrosirius 红染色切片的定量,证实了 LGUN 组心脏存在间质纤维化。因此,我们已经表明,妊娠晚期母体营养不良可能导致胎儿右心室心肌重构的发生,从而对右心室功能和生命后期的心脏健康产生负面影响。