The purpose of this project is to test the hypothesis that maternal and fetal glucose supplies to the placenta regulate placental oxidative and non-oxidative metabolism of carbon substrates. These studies are important because of the essential role of the placenta in nutritive exchange between the mother and fetus, the remarkably high oxygen and substrate consumption rates of the placenta, and the major quantitative contribution of glucose to placental carbon substrate utilization. Studies will be conducted in pregnant sheep over the second half of gestation using chronically catheterized preparations during short and long-term experiments.
Two specific aims will be addressed: 1) to test in vivo the hypothesis that glucose supply to the placenta regulates placental glucose consumption, the production of other carbon compounds, and placental carbon accretion; 2) to test in vivo the hypothesis that glucose supply to the placenta regulates placental glucose oxidation and the oxidation of other carbon compounds. In vivo studies will use Fick principle, radioactive and stable isotopic tracer, and glucose/insulin clamp techniques to quantify net fluxes of substrates and substrate interconversions as regulated by placental glucose supply and insulin concentrations in maternal and fetal circulations. Because variation in maternal (and thus fetal) plasma glucose concentration in pregnancy, particularly in pathologic states such as starvation, fasting, and especially diabetes mellitus, are frequent and often extreme, understanding of the effect of glycemia and thus placental glucose supply on placental metabolic function is essential for determining how the placenta provides for fetal nutritional needs, fetal metabolism and growth, and fetal well-being.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD028794-04
Application #
2201312
Study Section
Reproductive Biology Study Section (REB)
Project Start
1992-02-01
Project End
1997-01-31
Budget Start
1995-02-01
Budget End
1996-01-31
Support Year
4
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Pediatrics
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Rozance, Paul J; Limesand, Sean W; Barry, James S et al. (2009) Glucose replacement to euglycemia causes hypoxia, acidosis, and decreased insulin secretion in fetal sheep with intrauterine growth restriction. Pediatr Res 65:72-8
Hay Jr, William W (2008) Strategies for feeding the preterm infant. Neonatology 94:245-54
Rozance, Paul J; Limesand, Sean W; Barry, James S et al. (2008) Chronic late-gestation hypoglycemia upregulates hepatic PEPCK associated with increased PGC1alpha mRNA and phosphorylated CREB in fetal sheep. Am J Physiol Endocrinol Metab 294:E365-70
Rozance, Paul J; Limesand, Sean W; Zerbe, Gary O et al. (2007) Chronic fetal hypoglycemia inhibits the later steps of stimulus-secretion coupling in pancreatic beta-cells. Am J Physiol Endocrinol Metab 292:E1256-64
Hay Jr, William W (2006) Placental-fetal glucose exchange and fetal glucose metabolism. Trans Am Clin Climatol Assoc 117:321-39; discussion 339-40
Hay, W W (2006) Early postnatal nutritional requirements of the very preterm infant based on a presentation at the NICHD-AAP workshop on research in neonatology. J Perinatol 26 Suppl 2:S13-8
Regnault, Timothy R H; Hay Jr, William W (2006) In vivo techniques for studying fetoplacental nutrient uptake, metabolism, and transport. Methods Mol Med 122:207-24
Rozance, Paul J; Hay, William W (2006) Hypoglycemia in newborn infants: Features associated with adverse outcomes. Biol Neonate 90:74-86
Rozance, Paul J; Limesand, Sean W; Hay Jr, William W (2006) Decreased nutrient-stimulated insulin secretion in chronically hypoglycemic late-gestation fetal sheep is due to an intrinsic islet defect. Am J Physiol Endocrinol Metab 291:E404-11
Hay Jr, William W (2005) Intravenous nutrition of the very preterm neonate. Acta Paediatr Suppl 94:47-56

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