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Am J Physiol Regul Integr Comp Physiol 284: R245-R258, 2003; doi:10.1152/ajpregu.00108.2002
0363-6119/03 $5.00
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Vol. 284, Issue 2, R245-R258, February 2003

INVITED REVIEW
Possible mechanisms underlying pregnancy-induced changes in uterine artery endothelial function

Ian M. Bird1,2, Lubo Zhang3, and Ronald R. Magness1,2,4

1 University of Wisconsin-Madison, Department of Obstetrics and Gynecology, Perinatal Research Laboratories and the 2 Department of Pediatrics and 4 Animal Sciences, Madison, Wisconsin 53715; and 3 Center for Perinatal Biology, Department of Pharmacology and Physiology, Loma Linda University School of Medicine, Loma Linda, California 92350

The last 10 years has seen a dramatic increase in our understanding of the mechanisms underlying the pregnancy-specific adaptation in cardiovascular function in general and the dramatic changes that occur in uterine artery endothelium in particular to support the growing fetus. The importance of these changes is clear from a number of studies linking restriction of uterine blood flow (UBF) and/or endothelial dysfunction and clinical conditions such as intrauterine growth retardation (IUGR) and/or preeclampsia in both humans and animal models; these topics are covered only briefly here. The recent developments that prompts this review are twofold. The first is advances in an understanding of the cell signaling processes that regulate endothelial nitric oxide synthase (eNOS) in particular (Govers R and Rabelink TJ. Am J Physiol Renal Physiol 280: F193-F206, 2001). The second is the emerging picture that uterine artery (UA) endothelial cell production of nitric oxide (NO) as well as prostacyclin (PGI2) may be as much a consequence of cellular reprogramming at the level of cell signaling as due to tonic stimuli inducing changes in the level of expression of eNOS or the enzymes of the PGI2 biosynthetic pathway (cPLA2, COX-1, PGIS). In reviewing just how we came to this conclusion and outlining the implications of such a finding, we draw mostly on data from ovine or human studies, with reference to other species only where directly relevant.

nitric oxide; prostacyclin; calcium; kinases; programming


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