Understanding Placental Adaptation to Maternal Malnutrition

了解胎盘对母亲营养不良的适应

• 批准号: 9753298
• 负责人: Michael Carey Satterfield
• 金额: $ 30.4万
• 依托单位: TEXAS A&M AGRILIFE RESEARCH
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-09-01 至 2021-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9753298
• 关键词: Adult; Agriculture; Amino Acids; Angiogenic Factor; Animal Feed; Animal Model; Animals; Arteries; Biological; Biological Markers; Biological Models; Blood Vessels; Blood flow; Body Size; Breeding; Collaborations; Complex; Development; Diagnostic; Domestic Animals; Embryo; Endothelial Cells; Environment; Exhibits; Female; Fetal Development; Fetal Growth; Fetal Growth Retardation; Fetal Weight; Fetus; Foundations; Gases; Gene Expression; Genes; Genetic; Genotype; Goals; Growth; Growth and Development function; Health; Hormonal; Hormones; Human; Impairment; In Vitro; Incidence; Individual; Intervention; Knowledge; Life; Livestock; Malnutrition; Medical Care Costs; Metabolic; Metabolism; Molecular; Molecular Biology Techniques; Morbidity - disease rate; Mothers; Neonatal Mortality; Newborn Infant; Nutrient; Nutritional Study; Onset of illness; Operative Surgical Procedures; Outcome; Pathway interactions; Physiological; Placenta; Placental Biology; Placentation; Play; Population; Pregnancy; Prenatal Nutrition; Production; Reproductive Biology; Research; Research Personnel; Resources; Role; Selection Criteria; Series; Sheep; Small for Gestational Age Infant; Study models; Systems Biology; Testing; Time; Uterus; Weight; Work; angiogenesis; at-risk pregnancies; base; biomarker development; biomarker identification; cost; fetal; genetic selection; human subject; innovation; insight; male; maternal nutrient restriction; mortality; multidisciplinary; neonatal morbidity; novel; nutrient metabolism; nutrition; nutrition related genetics; offspring; pregnant; public health relevance; response; therapeutic development; tool; wasting

 DESCRIPTION (provided by applicant): In domestic animals and humans, optimal fetal growth is predicated on sufficient nutrient delivery across the placenta. Our long-range goal is to discover and understand the hormonal, cellular, and molecular mechanisms regulating placental growth and function to support optimal fetal growth. Importantly, impaired fetal growth is associated with increased incidence of neonatal morbidity and mortality in both livestock species and humans. In addition, emerging evidence related to developmental origins of adult-onset disease highlight the additional long- term consequences of a poor uterine environment on lifelong health. The goal of this proposal is to capitalize on natural population variance using the sheep, (serving as both an agriculturally important food animal as well as an accepted biomedical model for studies related to humans) to elucidate the mechanisms by which the placenta can adapt to maternal malnutrition to support varying degrees of fetal growth. To achieve this goal we will conduct a series of nutritional studies using singleton pregnant ewes of similar body size and condition, carrying embryos generated from similar males and superovulated donor females. We have previously employed this strategy and observed increased variance in levels of fetal growth in nutrient restricted ewes. We will capitalize on thi natural population variance by comparing the upper and lower quartiles of individuals based upon fetal growth to elucidate mechanisms controlling placental growth and function. Specific aims are to: 1) elucidate the relative contributions of fetal genotype and the host uterine environment on fetal development; 2) investigate mechanisms governing placental vascular growth and function in nutrient-restricted ewes; and 3) identify the contribution of select nutriens in regulating placental growth and function in nutrient-restricted ewes. This research is innovative because it will develop a unique animal model for the study of placental growth, function, and adaptation. In addition, we will employ novel surgical strategies allowing for retrospective analysis of early placental gene expression based on rates of fetal growth in late gestation. Completion of the proposed research is expected to fill a critical gap in our existing knowledge by providing novel insights into placental growth and function as they relate to the spectrum of observed rates of fetal growth. Translational outcomes of the proposed research include biomarkers for placental function as well as the identification of novel nutritional and genetic targets for the development of therapeutic strategies to enhance fetal growth in undernourished mothers.



项目成果

An electron microscopic study of myelination of pyramidal fibres at the level of the pyramidal decussation in the human fetus.

人类胎儿锥体交叉水平锥体纤维髓鞘形成的电子显微镜研究。

• 发表时间: 1982
• 期刊: Journal fur Hirnforschung
• 作者: Wózniak,W;O'Rahilly,R
• 通讯作者: O'Rahilly,R

Identification of Pathways Associated with Placental Adaptation to Maternal Nutrient Restriction in Sheep.

• DOI: 10.3390/genes11091031
• 发表时间: 2020-09-02
• 期刊: Genes
• 影响因子: 3.5
• 作者: Edwards AK;Dunlap KA;Spencer TE;Satterfield MC
• 通讯作者: Satterfield MC

Effect of maternal nutrient restriction on expression of glucose transporters (SLC2A4 and SLC2A1) and insulin signaling in skeletal muscle of SGA and Non-SGA sheep fetuses.

• DOI: 10.1016/j.domaniend.2020.106556
• 发表时间: 2020-10
• 期刊: Domestic animal endocrinology
• 影响因子: 2.1
• 作者: C. Sandoval;K. Askelson;C. Lambo;K. Dunlap;M. Satterfield

Placental Transcriptome Adaptations to Maternal Nutrient Restriction in Sheep.

• DOI: 10.3390/ijms22147654
• 发表时间: 2021-07-17
• 期刊: International journal of molecular sciences
• 影响因子: 5.6
• 作者: Steinhauser CB;Lambo CA;Askelson K;Burns GW;Behura SK;Spencer TE;Bazer FW;Satterfield MC
• 通讯作者: Satterfield MC

Maternal Nutrient Restriction and Skeletal Muscle Development: Consequences for Postnatal Health.

• DOI: 10.1007/978-3-030-45328-2_9
• 发表时间: 2020
• 期刊: Advances in experimental medicine and biology
• 作者: C. Sandoval;Guoyao Wu;Stephen B Smith;K. Dunlap;M. Satterfield