Prostaglandin inhibition prevents the fall in pulmonary vascular resistance as a result of rhythmic distension of the lungs in fetal lambs
- PMID: 1891282
- DOI: 10.1203/00006450-199107000-00013
Prostaglandin inhibition prevents the fall in pulmonary vascular resistance as a result of rhythmic distension of the lungs in fetal lambs
Abstract
Prostaglandins (PG) are vasoactive factors involved in the regulation of pulmonary vascular resistance at birth. However, their physiologic importance is unclear. We hypothesized that PG are important regulators of pulmonary vascular resistance during static and rhythmic distension of the lungs. To test this hypothesis, we studied seven near-term fetal lambs treated with meclofenamate (a PG synthetase inhibitor) and six controls. The fetal lambs were instrumented on a long-term basis with vascular catheters to measure pulmonary arterial pressures, left atrial pressures, and pulmonary blood flow (radionuclide-labeled microsphere method). The fetal airway was intubated, and the ductus arteriosus wall was infiltrated with formalin to assure full patency during the study period. Pulmonary vascular resistance was calculated during baseline and during sequential in utero static distension of the fetal lungs, rhythmic distension, and ventilation with oxygenation. We found that during rhythmic distension, inhibition of PG synthesis abolished the 4-fold decrease in pulmonary vascular resistance seen in the control group. In contrast, during static distension, pulmonary vascular resistance did not change in either group, and during ventilation with oxygenation, pulmonary vascular resistance decreased 12-fold in both groups. We conclude that PG are important regulators of pulmonary vascular resistance during rhythmic distension but are not essential for the regulation of pulmonary vascular resistance during static distension or during ventilation with oxygenation.
Similar articles
-
Bradykinin receptor blockade does not affect oxygen-mediated pulmonary vasodilation in fetal lambs.Pediatr Res. 1994 Oct;36(4):474-80. doi: 10.1203/00006450-199410000-00010. Pediatr Res. 1994. PMID: 7816523
-
EDRF inhibition attenuates the increase in pulmonary blood flow due to oxygen ventilation in fetal lambs.J Appl Physiol (1985). 1992 Nov;73(5):2151-7. doi: 10.1152/jappl.1992.73.5.2151. J Appl Physiol (1985). 1992. PMID: 1474097
-
Endothelin receptor blockade does not alter the increase in pulmonary blood flow due to oxygen ventilation in fetal lambs.Pediatr Res. 1996 Jul;40(1):152-7. doi: 10.1203/00006450-199607000-00026. Pediatr Res. 1996. PMID: 8798262
-
Prostaglandins, related compounds, and the perinatal pulmonary circulation.Clin Perinatol. 1984 Oct;11(3):565-79. Clin Perinatol. 1984. PMID: 6386270 Review.
-
Control of the pulmonary circulation in the fetus and during the transitional period to air breathing.Eur J Obstet Gynecol Reprod Biol. 1999 Jun;84(2):127-32. doi: 10.1016/s0301-2115(98)00321-2. Eur J Obstet Gynecol Reprod Biol. 1999. PMID: 10428335 Review.
Cited by
-
Modulation of pulmonary vasomotor tone in the fetus and neonate.Respir Res. 2001;2(3):139-44. doi: 10.1186/rr50. Epub 2001 Mar 8. Respir Res. 2001. PMID: 11686877 Free PMC article. Review.
-
Pulmonary Vascular Phenotypes of Prematurity: The Path to Precision Medicine.J Pediatr. 2023 Aug;259:113444. doi: 10.1016/j.jpeds.2023.113444. Epub 2023 Apr 25. J Pediatr. 2023. PMID: 37105409 Free PMC article.
-
Pulmonary Hypertension: The Hidden Danger for Newborns.Neonatology. 2021;118(2):211-217. doi: 10.1159/000516107. Epub 2021 May 5. Neonatology. 2021. PMID: 33951650 Free PMC article. Review.
-
Molecular mechanisms regulating the vascular prostacyclin pathways and their adaptation during pregnancy and in the newborn.Pharmacol Rev. 2012 Jul;64(3):540-82. doi: 10.1124/pr.111.004770. Epub 2012 Jun 7. Pharmacol Rev. 2012. PMID: 22679221 Free PMC article. Review.
-
Pulmonary hemodynamic responses to in utero ventilation in very immature fetal sheep.Respir Res. 2010 Aug 19;11(1):111. doi: 10.1186/1465-9921-11-111. Respir Res. 2010. PMID: 20723253 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources