Permanent Anatomic Closure of the Ductus Arteriosus in Newborn Baboons: The Roles of Postnatal Constriction, Hypoxia, and Gestation
- 1 January 1999
- journal article
- Published by Springer Nature in Pediatric Research
- Vol. 45 (1) , 19-29
- https://doi.org/10.1203/00006450-199901000-00005
Abstract
Permanent closure of the ductus arteriosus require loss of cells from the muscle media and development of neointimal mounds, composed in part of proliferating endothelial cells. We hypothesized that postnatal ductus constriction produces hypoxia of the inner vessel wall; we also hypothesized that hypoxia might lead to cell death and the production of vascular endothelial cell growth factor (VEGF), a hypoxia-inducible growth factor that stimulates endothelial proliferation. We mapped the distribution of hypoxia in newborn baboons and correlated it with the appearance of cell death (TUNEL technique), VEGF expression, and endothelial proliferation (proliferating cell nuclear antigen expression). In the full-term baboon (n = 10), the ductus was functionally closed on Doppler examination by 24 h after delivery. Regions of the ductus where the lumen was most constricted were associated with moderate/intense hypoxia; VEGF expression was increased in the hypoxic muscle media, and luminal endothelial cells, adjacent to the hypoxic media, were proliferating. Cells in the most hypoxic regions of the ductus wall were undergoing DNA fragmentation. In contrast, regions of the ductus with mild degrees of hypoxia had no evidence of cell death, VEGF expression, or endothelial proliferation. Cell death and endothelial proliferation seemed to be limited to regions of the full-term ductus experiencing moderate/intense hypoxia. In the premature baboon (67% gestation) (n = 24), only 29% closed their ductus by Doppler examination before d 6. None of the premature baboons, including those with a closed ductus by Doppler, had evidence of moderate/intense hypoxia; also, there was no evidence of cell death, VEGF expression, endothelial proliferation, or neointima formation by d 6. Therefore, the premature ductus is resistant to developing hypoxia, even when its lumen is constricted; this may make it susceptible to later reopening.Keywords
This publication has 31 references indexed in Scilit:
- Regulation of Ductus Arteriosus Patency by Nitric Oxide in Fetal Lambs: The Role of Gestation, Oxygen Tension, and Vasa VasorumPediatric Research, 1998
- Changes in Endothelial Cell and Smooth Muscle Cell Integrin Expression during Closure of the Ductus Arteriosus: An Immunohistochemical Comparison of the Fetal, Preterm Newborn, and Full-Term Newborn Rhesus Monkey DuctusPediatric Research, 1996
- Transforming Growth Factor-β Protein and Messenger RNA Expression Is Increased in the Closing Ductus ArteriosusPediatric Research, 1996
- Factors determining reopening of the ductus arteriosus after successful clinical closure with indomethacinThe Journal of Pediatrics, 1995
- Formation of intimal cushions in the ductus arteriosus as a model for vascular intimal thickening. An immunohistochemical study of changes in extracellular matrix componentsAtherosclerosis, 1992
- Ultrastructural and immunohistochemical changes of the extracellular matrix during intimal cushion formation in the ductus arteriosus of the dogAtherosclerosis, 1989
- Factors determining the loss of ductus arteriosus responsiveness to prostaglandin E.Circulation, 1983
- Prostaglandin E1 infants with ductus arteriosus-dependent congenital heart disease.Circulation, 1981
- Oral prostaglandin E2 in ductus-dependent pulmonary circulation.Circulation, 1981
- The ductus arteriosus in the preterm infant: Histologic and clinical observationsThe Journal of Pediatrics, 1980