Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Biol Reprod ; 72(3): 720-6, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15548732

RESUMEN

The etiology of fetal membrane (FM) rupture is unknown. A hypothesis that the FM weakens by a process of collagen remodeling and apoptosis to facilitate rupture has been proposed. Human FMs reportedly exhibit a zone of altered histology, postulated to be the FM rupture site, but concomitant FM weakness has not been demonstrated. We hypothesized that a discrete zone of FM with marked weakness, histological change, and evidence of remodeling and apoptosis, develops in late gestation in the FM overlying the cervix. FM tissue from women undergoing prelabor cesarean delivery were perioperatively marked to identify the FM overlying the cervix, cut with a procedure that facilitates remapping the rupture strength of FM pieces to their former location and orientation on a three-dimensional model, and tested for strength. A 10-cm FM zone centered at the cervical mark was compared with the remaining FM. Mean rupture strength within the cervical zone was 55% of the remaining FM. The cervical zone also exhibited increased MMP-9 protein, decreased tissue inhibitor of metalloproteinases-3 (TIMP-3) protein, and increased PARP cleavage coincident with the previously reported zone of altered histology. A discrete zone of weakness is present in term prelabor FMs overlying the cervix and has biochemical characteristics consistent with tissue remodeling and apoptosis.


Asunto(s)
Cuello del Útero/metabolismo , Membranas Extraembrionarias/metabolismo , Inicio del Trabajo de Parto/fisiología , Rotura Espontánea/metabolismo , Apoptosis/fisiología , Colágeno/metabolismo , Membranas Extraembrionarias/citología , Femenino , Humanos , Metaloproteinasa 9 de la Matriz/metabolismo , Placenta/metabolismo , Embarazo , Valores de Referencia , Resistencia a la Tracción/fisiología , Distribución Tisular , Inhibidor Tisular de Metaloproteinasa-3/metabolismo , Útero/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA