Submitted August 16, 2007
Returned for revision September 6, 2007
Accepted November 20, 2007
Pregnancy
Regulation of Maternal and Fetal Hemodynamics by Heme Oxygenase in Mice
Hui Zhao *,
Ronald J Wong ,
Timothy C Doyle ,
Nihar Nayak ,
Hendrik J Vreman ,
Christopher H Contag ,
and
David K Stevenson
* To whom correspondence should be addressed. E-mail: huizhao2{at}stanford.edu.
Abstract
Heme oxygenase (HMOX) regulates vascular tone and blood pressure through the production of carbon monoxide (CO), a vasodilator derived from the heme degradation pathway. During pregnancy, the maternal circulation undergoes significant adaptations to accommodate for the hemodynamic demands of the developing fetus. Our objective was to investigate the role of HMOX on maternal and fetal hemodynamics during pregnancy in a mouse model. We measured and compared maternal tissue and placental HMOX activity and endogenous CO production, represented by excreted CO and carboxyhemoglobin levels, during pregnancy (E12.5-15.5) to non-pregnant controls. Micro-ultrasound was used to monitor maternal abdominal aorta diameters as well as blood flow velocities and diameters of fetal umbilical arteries. Tin mesoporphyrin, a potent HMOX inhibitor, was used to inhibit HMOX activity. Changes in maternal vascular tone were monitored by tail cuff blood pressure measurements. Effects of HMOX inhibition on placental structures were assessed by histology. We showed that maternal tissue and placental HMOX activity and CO production were significantly elevated during pregnancy. When HMOX in the placenta was inhibited, maternal and fetal hemodynamics underwent significant changes with maternal blood pressures increasing. We conclude that increases in maternal tissue and placental HMOX activity contribute to the regulation of peripheral vascular resistance, and therefore are important for the maintenance of normal maternal vascular tone and fetal hemodynamic functions during pregnancy.
Key words:
Pregnancy
Placenta
Carbon Monoxide
Heme Oxygenase
Hemodynamics