The long term objective of this project is to determine those factors in the maternal and fetal compartments responsible for maintaining and regulating uteroplacental (UtBF) and umbilicoplacental blood flow, and how they relate to general cardiovascular adaptation during pregnancy. In the proposed funding period, efforts will be focused on 3 main areas: the vascular effects of estrogen, angiotensin II (ANG II) receptor (ATR) expression and function, and smooth muscle protein expression and function. To do this 5 Specific Aims will be addressed: 1)to determine the role of nitric oxide, cGMP and K+ channels in mediating estrogen- induced vasodilation and modulation of UtBF in pregnancy; 2) to clarify what peripherally released vasoconstrictor(s) mediates ANG II induced uterine vasoconstriction; 3) to determine how vascular smooth muscle ATR expression is regulated in pregnancy; 4) to investigate the hormonal and/or growth factors and inhibitors of cell division that account for uterine vascular growth and hypertrophy in pregnancy; and 5) to examine the role and mechanism whereby estrogen may modulate uteroplacental and umbilicoplacental blood flows prior to and during parturition. To achieve these aims we will study chronically instrumented nonpregnant ewes and pregnant ewes with their fetus. In vivo studies are designed to answer specific questions about physiologic responses to and mechanisms of action by estrogen, ANG II or alpha-agonists in maternal uterine circulation, and the effects of parturition on both maternal and fetal placental vasculature. In vitro studies using tissues from these animals with patch-clamp techniques, contractile protein measurements, western or northern analysis, cell cultures, and measurement of vascular stresses will permit us to more accurately determine the cellular and molecular mechanisms responsible for adaptive changes to pregnancy. The results of the proposed studies will provide important insights into biochemical cellular and physiologic adaptive mechanisms that are necessary for the successful outcome of pregnancy and the maintenance of fetal well-being, which in turn will improve our understanding of problems associated with abnormal pregnancy and development, thereby permitting us to address them in a more meaningful way.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD008783-26
Application #
6387432
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Program Officer
Ilekis, John V
Project Start
1977-09-01
Project End
2003-06-30
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
26
Fiscal Year
2001
Total Cost
$333,851
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Pediatrics
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Lechuga, Thomas J; Zhang, Hong-hai; Sheibani, Lili et al. (2015) Estrogen Replacement Therapy in Ovariectomized Nonpregnant Ewes Stimulates Uterine Artery Hydrogen Sulfide Biosynthesis by Selectively Up-Regulating Cystathionine ?-Synthase Expression. Endocrinology 156:2288-98
Rosenfeld, Charles R; Roy, Timothy (2014) Prolonged uterine artery nitric oxide synthase inhibition modestly alters basal uteroplacental vasodilation in the last third of ovine pregnancy. Am J Physiol Heart Circ Physiol 307:H1196-203
Rosenfeld, Charles R; Hynan, Linda S; Liu, Xiao-tie et al. (2014) Large conductance Ca2+-activated K+ channels modulate uterine ?1-adrenergic sensitivity in ovine pregnancy. Reprod Sci 21:456-64
Rosenfeld, Charles R; DeSpain, Kevin; Liu, Xiao-tie (2012) Defining the differential sensitivity to norepinephrine and angiotensin II in the ovine uterine vasculature. Am J Physiol Regul Integr Comp Physiol 302:R59-67
Rosenfeld, Charles R; DeSpain, Kevin; Word, R Ann et al. (2012) Differential sensitivity to angiotensin II and norepinephrine in human uterine arteries. J Clin Endocrinol Metab 97:138-47
Rosenfeld, Charles R; Roy, Timothy (2012) Large conductance Ca2+-activated and voltage-activated K+ channels contribute to the rise and maintenance of estrogen-induced uterine vasodilation and maintenance of blood pressure. Endocrinology 153:6012-20
Khan, Liaqat H; Rosenfeld, Charles R; Liu, Xiao-Tie et al. (2010) Regulation of the cGMP-cPKG pathway and large-conductance Ca2+-activated K+ channels in uterine arteries during the ovine ovarian cycle. Am J Physiol Endocrinol Metab 298:E222-8
Rosenfeld, Charles R; Liu, Xiao-tie; DeSpain, Kevin (2009) Pregnancy modifies the large conductance Ca2+-activated K+ channel and cGMP-dependent signaling pathway in uterine vascular smooth muscle. Am J Physiol Heart Circ Physiol 296:H1878-87
Miao, Darryl C; Velaphi, Sithembiso C; Roy, Timothy et al. (2008) Metabolism and synthesis of arginine vasopressin in conscious newborn sheep. Am J Physiol Endocrinol Metab 295:E672-7
Rosenfeld, Charles R; Word, R Ann; DeSpain, Kevin et al. (2008) Large conductance Ca2+-activated K+ channels contribute to vascular function in nonpregnant human uterine arteries. Reprod Sci 15:651-60

Showing the most recent 10 out of 90 publications