Browse by author
Lookup NU author(s): Professor Michael Taggart
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Objective: Endogenous uterine agonists can activate numerous signaling pathways to effect increased force. Our objective was to assess expression of key constituents of these pathways, in alliance with contractile function, through late gestation and during term and preterm labor. Study Design: Using myography, we measured the response to three agonists compared to depolarization alone (K+, 124 mM) and calculated agonist/depolarization ratio (ADR). We measured gene expression using qRT-PCR. Results: Contractile responsiveness to depolarization alone, oxytocin or endothelin-1 increased during pregnancy compared to non-pregnant animals. ADR did not change during uterine activation or parturition. Inhibition of ROK decreased responses to OT in all tissues but significantly more during uterine activation. Expression of rhoA and ROK was increased significantly in active labor at term or preterm. Conclusions: The rhoA/ROK pathway is a key regulator of uterine activation during labor and may be a useful target for prevention of spontaneous preterm birth.
Author(s): Taggart MJ, Arthur P, Zielnik B, Mitchell BF
Publication type: Article
Publication status: Published
Journal: American Journal of Obstetrics and Gynecology
Print publication date: 08/05/2012
ISSN (print): 0002-9378
ISSN (electronic): 1097-6868
Publisher: Mosby, Inc.
Altmetrics provided by Altmetric