Velvis H, Moore P, Heymann M A
Cardiovascular Research Institute, University of California San Francisco 94143.
Pediatr Res. 1991 Jul;30(1):62-8. doi: 10.1203/00006450-199107000-00013.
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.
前列腺素(PG)是参与出生时肺血管阻力调节的血管活性因子。然而,它们的生理重要性尚不清楚。我们假设PG在肺的静态和节律性扩张过程中是肺血管阻力的重要调节因子。为了验证这一假设,我们研究了7只接受甲氯芬那酸(一种PG合成酶抑制剂)治疗的近足月胎羊和6只对照组胎羊。长期用血管导管对胎羊进行监测,以测量肺动脉压、左心房压和肺血流量(放射性核素标记微球法)。将胎儿气道插管,并向动脉导管壁注入福尔马林,以确保在研究期间完全通畅。在基线期以及在子宫内对胎儿肺进行序贯静态扩张、节律性扩张和充氧通气期间计算肺血管阻力。我们发现,在节律性扩张期间,PG合成的抑制消除了对照组中肺血管阻力4倍的下降。相比之下,在静态扩张期间,两组的肺血管阻力均未改变,在充氧通气期间,两组的肺血管阻力均下降了12倍。我们得出结论,PG在节律性扩张期间是肺血管阻力的重要调节因子,但在静态扩张或充氧通气期间对肺血管阻力的调节并非必不可少。