The uterine myocyte as a target for prevention of preterm birth


prematurity, preterm labour, myosin regulatory light chain, rhoA-associated kinase, tocolysis, uterine contractility

B.F. Mitchell1,2, H.N. Aguilar2, A. Mosher3, S. Wood4, D.M. Slater3
University of Alberta Departments of Obstetrics and Gynecology1 and of Physiology2, Edmonton AB and University of Calgary Department of Physiology and Pharmacology3 and of Obstetrics and Gynecology4, Calgary AB Canada

Correspondence at:


Preterm birth (PTB) remains the most common cause of neonatal morbidity and mortality as well as long-term disability. Current strategies to prevent or arrest spontaneous preterm labor (SPTL) have limited success. For almost three decades, there have been no novel pharmacological agents used clinically to address this important obstetrical complication. In this review, we focus on the uterine myocyte as a target for prevention of spontaneous PTB. After presenting an overview of intracellular signaling pathways that are important in regulation of smooth muscle ­contractility, we discuss previous and current pharmacological approaches to manage SPTL. We also present recent evidence from our own laboratories suggesting a potentially novel and uterine-specific approach to maintain or ­impose uterine relaxation. Finally, we briefly discuss extrinsic systems that might affect uterine activity and reinforce the concept that SPTL represents a syndrome that is the end result of a variety of pathophysiologic etiologies leading to PTB. We conclude by emphasizing the need for much more research to provide sufficient understanding of the mechanisms of SPTL and to make inroads towards reducing the incidence and adverse consequences of this common and serious syndrome.