Obstetric complications resulting in reduced uteroplacental perfusion greatly increase fetal mortality. Under these circumstances, fetal vascular adjustments are required to maintain adequate perfusion of organs critical for the normal growth and development of the fetus. The fetus responds to hypoxemia by redistributing cardiac output to organs such as the heart, brain, and adrenal gland The vascular mechanisms underlying this redistribution are poorly understood. In the adult circulation, the endothelium modulates vascular tone by release of vasoactive substances and is influenced by changes in oxygen tension. We hypothesize that fetal endothelium modulates vascular tone by releasing vasoactive autacoids in response to changes in oxygen tension. We further hypothesize that, in vivo, the fetal endothelium is an important oxygen sensing site and influences vascular reactivity to circulating hormones via oxygen-sensitive mechanisms. The effect of changes in oxygen tension on endothelium-dependent relaxation and agonist-induced contraction will be measured in isolated carotid and pulmonary arteries from guinea pig fetuses from 0.5 to near term gestation. Further, the vascular responses of isolated perfused mesenteric preparations will be measured to study reactivity of resistance-sized arteries. The response of the endothelium to changes in oxygen will be investigated in arteries from newborn and adult guinea pigs to characterize the adaptive changes in the endothelium after birth.
SPECIFIC AIMS : 1) To determine the effect of gestational age on endothelium-dependent mechanisms in fetal arteries. 2) To determine the effect of oxygen on endothelium-dependent modulation of contraction and relaxation of isolated fetal arteries. 3) To determine the effect of maturation on oxygen sensitivity of the endothelium between fetal, newborn, and adult arteries.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29HL049999-01
Application #
3474130
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Project Start
1993-05-01
Project End
1997-04-30
Budget Start
1993-05-01
Budget End
1994-04-30
Support Year
1
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Evans, LaShauna C; Liu, Hongshan; Thompson, Loren P (2012) Differential effect of intrauterine hypoxia on caspase 3 and DNA fragmentation in fetal guinea pig hearts and brains. Reprod Sci 19:298-305
Thompson, Loren; Dong, Yafeng; Evans, Lashauna (2009) Chronic hypoxia increases inducible NOS-derived nitric oxide in fetal guinea pig hearts. Pediatr Res 65:188-92