Thorson Jennifer F, Prezotto Ligia D
Nutrition, Growth and Physiology Research Unit, U.S. Meat Animal Research Center, USDA, Agricultural Research Service, Clay Center, NE, United States.
Physiology Laboratory, Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, United States.
Front Physiol. 2024 Dec 5;15:1501309. doi: 10.3389/fphys.2024.1501309. eCollection 2024.
Malnutritional stress during gestation is a well-established driver of metabolic disfunction in offspring. Extended exposure to malnutrition requires metabolic plasticity as the animal shifts toward a catabolic state. In this paper we demonstrate the influence of malnutrition throughout gestation on uterine artery hemodynamics and the metabolism of the dam and neonate. We hypothesized that gestational malnutrition reduces blood flow of the maternal uterine artery and regulates the metabolic profile of the dam and offspring. Further, the combination of these factors consequently influences the concentration of metabolites in the cerebrospinal fluid of the neonate at birth. To test our hypotheses, pregnant cows caring a single female fetus were assigned to treatments by age and body condition score to one of three individually-fed dietary treatments: Underfed, Control, or Overfed throughout gestation. Uterine blood flow was measured via transrectal Doppler ultrasonography in late gestation. Blood samples were collected from dams throughout gestation, and blood and cerebrospinal fluid were collected from neonates at birth to analyze concentration of metabolites. In the current report, we reveal that maternal malnutrition regulates uterine artery hemodynamics and the maternal metabolic profile throughout gestation. This is the first report to demonstrate that maternal undernutrition leads to an increase in the concentration of urea nitrogen in neonates. Finally, a concentration gradient of metabolites from the dam to neonatal cerebrospinal fluid was observed, which may have potential implications for central nervous system development. These findings not only illustrate the complexity of the maternal-to-fetal interaction required to support the growth of the fetus and homeostasis of the dam but also reveals a novel avenue for investigating the influence of protracted maternal malnutrition on metabolic pathway preferences in offspring. Moreover, these findings are of paramount importance in the development of intervention strategies for morbid neonates.
孕期的营养不良应激是子代代谢功能障碍的一个公认驱动因素。长期暴露于营养不良状态需要代谢可塑性,因为动物会转向分解代谢状态。在本文中,我们证明了孕期全程营养不良对子宫动脉血流动力学以及母体和新生儿代谢的影响。我们假设孕期营养不良会减少母体子宫动脉的血流量,并调节母体和子代的代谢谱。此外,这些因素的综合作用会影响新生儿出生时脑脊液中的代谢物浓度。为了验证我们的假设,将怀有单胎雌性胎儿的怀孕母牛按年龄和体况评分分配到三种单独饲喂的饮食处理之一:孕期全程营养不良、对照或过量饲喂。在妊娠后期通过经直肠多普勒超声测量子宫血流量。在孕期全程从母体采集血样,在出生时从新生儿采集血样和脑脊液以分析代谢物浓度。在本报告中,我们揭示了母体营养不良在孕期全程调节子宫动脉血流动力学和母体代谢谱。这是第一份证明母体营养不良会导致新生儿尿素氮浓度升高的报告。最后,观察到从母体到新生儿脑脊液的代谢物浓度梯度,这可能对中枢神经系统发育具有潜在影响。这些发现不仅说明了支持胎儿生长和母体稳态所需的母胎相互作用的复杂性,还揭示了一条研究长期母体营养不良对后代代谢途径偏好影响的新途径。此外,这些发现在病态新生儿干预策略的制定中至关重要。