Stead Family Department of Pediatrics, University of Iowa, Iowa City, IA, United States; Iowa Inflammation Program, University of Iowa, Iowa City, IA, United States.
UmojaBiopharma, Seattle, WA, United States.
J Nutr. 2024 Jul;154(7):2065-2075. doi: 10.1016/j.tjnut.2024.05.021. Epub 2024 May 24.
Iron is crucial for growth and development, but excess iron is harmful. Neonatal mice have elevated concentrations of circulating iron, but the source of this iron is unclear. This lack of understanding makes it difficult to optimize early life iron balance.
Identify the origins of neonatal tissue-specific iron pools using dietary manipulation and cross-fostering murine models.
To determine whether tissue-specific neonatal iron was primarily acquired during gestation or after birth, pups born to iron-sufficient or iron-deficient dams were cross-fostered, and tissues were harvested at postnatal days 3-5 to measure iron content. A separate set of female mice were fed a diet enriched with the stable iron isotope 57 (Fe) for 4 generations to replace naturally abundant liver iron isotope 56 (Fe) stores with Fe. To quantify the proportions of neonatal iron acquired during gestation, pups born to dams with Fe or Fe stores were cross-fostered, and tissues were harvested at postnatal day 3-5 to determine Fe:Fe ratios by inductively coupled plasma mass spectrometry. Finally, to quantify the proportion of neonatal iron acquired from the maternal diet, female mice with Fe or Fe stores switched diets upon mating, and pup tissues were harvested on P0 to determine Fe:Fe ratios by inductively coupled plasma mass spectrometry.
Perinatal iron deficiency resulted in smaller pups, and gestational iron deficiency resulted in lower neonatal serum and liver iron. Cross-fostering between dams with Fe and Fe stores demonstrated that ≤70% of neonatal serum, liver, and brain iron were acquired during gestation. Dietary manipulation experiments using dams with Fe and Fe stores showed that over half of neonatal serum, liver, and brain iron were from the dam's gestational diet rather than preconception iron stores.
This study provides quantitative values for the sources of neonatal iron, which may inform approaches to optimize neonatal iron status.
铁对于生长和发育至关重要,但过量的铁是有害的。新生小鼠循环铁浓度升高,但铁的来源尚不清楚。这种缺乏认识使得难以优化生命早期的铁平衡。
使用饮食干预和交叉寄养鼠模型确定新生儿组织特异性铁池的来源。
为了确定组织特异性新生儿铁主要是在妊娠期间还是出生后获得的,将铁充足或铁缺乏的母鼠所生的幼崽进行交叉寄养,并在出生后第 3-5 天采集组织以测量铁含量。另一组雌性小鼠连续 4 代喂食富含稳定铁同位素 57(Fe)的饮食,以用 Fe 替代天然丰富的肝脏铁同位素 56(Fe)储存。为了量化妊娠期间获得的新生儿铁的比例,将 Fe 或 Fe 储存的母鼠所生的幼崽进行交叉寄养,并在出生后第 3-5 天采集组织,通过电感耦合等离子体质谱法确定 Fe:Fe 比值。最后,为了量化从母体饮食中获得的新生儿铁的比例,Fe 或 Fe 储存的雌性小鼠在交配时切换饮食,并在 P0 时采集幼崽组织,通过电感耦合等离子体质谱法确定 Fe:Fe 比值。
围产期铁缺乏导致幼鼠体重减轻,妊娠期铁缺乏导致新生儿血清和肝脏铁含量降低。Fe 和 Fe 储存的母鼠之间的交叉寄养表明,≤70%的新生儿血清、肝脏和大脑铁是在妊娠期间获得的。使用 Fe 和 Fe 储存的母鼠进行饮食干预实验表明,超过一半的新生儿血清、肝脏和大脑铁来自母鼠的妊娠期饮食,而不是孕前铁储存。
本研究提供了新生儿铁来源的定量值,这可能为优化新生儿铁状态的方法提供信息。