Preterm delivery before 37 weeks of gestation (PTD) is a major public health problem. There are 4.5 million deliveries in the US of which 11% occur prematurely. Despite extensive research and a multitude of interventions, the rate of PTD has actually increased over the past 20 years. No available labor inhibiting drug prolongs pregnancy more than 96h compared to placebo. High risk groups include substance abusers, adolescents, and members of low socioeconomic class and minorities. The refractory nature of the problem reflects its heterogeneous etiology and pathophysiology, which may require multiple distinct preventive and therapeutic approaches. Scientists based much of their past activities on the assumption preterm labor is the same as term labor, only ill-timed. One of the great reproductive mysteries is not why labor occurs at term, but why it does not occur much earlier in gestation in response to progressive stretching of the myometrium in response to the growing conceptus. Four myometrial phases are described across gestation: quiescence, activation, labor and involution. We suggest myometrial quiescence is an active process and have demonstrated a paracrine uterine quiescent factor (QF) that is synthesized and released from human and guinea pig chorion with biologic characteristics consistent with having principle reponsibility for uterine quiescence. Withdrawal of the QF would lead to premature myometrial activation and susceptability to preterm labor, and continued release at term would produce dysfunctional labor or post dates culminating in cesarean section and its attendent morbidity and costs. We propose 3 specific aims for a Phase I study. 1 - Isolate QF using traditional gel electrophoretic approaches and mass spectrometry; 2 - Protein characterization of QF; 3 - Synthesize or purify QF. We will then move rapidly, in Phase 2, to translational studies beginning with a test of the ability of either native or synthesized QF to inhibit preterm delivery in guinea pig. The outcome of this research will provide a deeper understanding of gestational regulation and lead to new targeted therapies to prevent PTD and reduce cesarean section for dysfunctional labor.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43HD049185-01A1
Application #
6933643
Study Section
Special Emphasis Panel (ZRG1-EMNR-E (10))
Program Officer
Ilekis, John V
Project Start
2005-05-15
Project End
2006-05-14
Budget Start
2005-05-15
Budget End
2006-05-14
Support Year
1
Fiscal Year
2005
Total Cost
$147,000
Indirect Cost
Name
Perinet, Inc.
Department
Type
DUNS #
145689266
City
Ruxton
State
MD
Country
United States
Zip Code
21204
Mason, Clifford W; Swaan, Peter W; Weiner, Carl P (2006) Identification of interactive gene networks: a novel approach in gene array profiling of myometrial events during guinea pig pregnancy. Am J Obstet Gynecol 194:1513-23
Weiner, Carl P; Mason, Clifford; Hall, Gentzon et al. (2006) Pregnancy and estradiol modulate myometrial G-protein pathways in the guinea pig. Am J Obstet Gynecol 195:275-87