The overall objective of this proposal is to study, during normal and pathological conditions, the role of the sympathetic system in modulating renal hemodynamics and renal function during development using chronically catheterized and conscious fetal, newborn and adult sheep. I) The first major objective of this proposal will be to test the hypothesis that the renal hemodynamic and functional responses to Alpha, Beta, and dopamine receptor stimulation differ between fetal, newborn and adult animals. More specifically, this proposal is designed to investigate the ability of renal Alpha, Beta, and dopaminergic receptors to (a) modulate renal vascular tone, and (b) glomerular filtration rate, sodium and water metabolism, and renin release during development. Intrarenal infusion of different Alpha, Beta and dopamine agonists and antagonists will be used. Moreover, (c) results from these in vivo experiments will be correlated to in vitro characterization of renal Alpha, Beta and dopaminergic receptors in fetal, newborn and adult sheep. II) The second major objective of this proposal is to determine the role of circulating catecholamines and sympathetic nervous system in the fetal renal response to hypoxemia. We are speculating that there is a hierarchy in the mechanisms controlling renal hemodynamics and function during fetal hypoxemia, renal nerve activation modulating acute changes and circulating catecholamines modulating long-term effects of hypoxemia. Moreover, we are suggesting that these mechanisms may have different developmental patterns. More specifically, we are proposing to study in young (less than 115 days gestation) and near-term (greater than 135 days gestation; term 145 days) fetal lambs (a) the role of renal nerves, and (b) the contribution of circulating catecholamines in modulating the renal hemodynamic and functional responses to severe (pO2 about 8 mmHg) and moderate (pO2 about 14 mmHg) hypoxemia. Moreover, (c) the role of renal prostaglandins in attenuating the effects of sympathetically mediated renal vasoconstriction during severe and moderate hypoxemia will be studied. In summary, understanding of the fetal and neonatal renal responsiveness to sympathetic stimulation a) may have immediate clinical relevance since adrenergic agents are presently used in neonatal intensive care situations, and b) is essential for the development of new concepts regarding intrauterine therapy and management of the fetus during high-risk pregnancies and of severely sick premature infants.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK043961-10
Application #
2143428
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Project Start
1985-09-30
Project End
1996-07-31
Budget Start
1995-04-20
Budget End
1996-07-31
Support Year
10
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Iowa
Department
Pediatrics
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
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Guillery, E N; Mathews, M S; Orlowski, J et al. (1996) Angiotensin II and the maturation of renal cortical Na+/H+ exchanger activity during fetal life in sheep. Am J Physiol 271:R1507-13
Nuyt, A M; Segar, J L; Holley, A T et al. (1996) Arginine vasopressin modulation of arterial baroreflex responses in fetal and newborn sheep. Am J Physiol 271:R1643-53
Guillery, E N; Karniski, L P; Mathews, M S et al. (1995) Role of glucocorticoids in the maturation of renal cortical Na+/H+ exchanger activity during fetal life in sheep. Am J Physiol 268:F710-7
Canessa, L M; Piccio, M M; Vachvanichsanong, P et al. (1995) Alpha 1B-adrenergic receptors in rat renal microvessels. Kidney Int 48:1412-9
Segar, J L; Bedell, K; Page, W V et al. (1995) Effect of cortisol on gene expression of the renin-angiotensin system in fetal sheep. Pediatr Res 37:741-6
Slobodyansky, E; Aoki, Y; Gaznabi, A K et al. (1995) Dopamine and protein phosphatase activity in renal proximal tubules. Am J Physiol 268:F279-84
Segar, J L; Merrill, D C; Robillard, J E (1994) Role of endogenous ANG II on resetting arterial baroreflex during development. Am J Physiol 266:H52-9
Robillard, J E; Schutte, B C; Page, W V et al. (1994) Ontogenic changes and regulation of renal angiotensin II type 1 receptor gene expression during fetal and newborn life. Pediatr Res 36:755-62

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