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Abstract 1749Poster Session I, Saturday, 5/1 (poster 106)
Angiotensin-converting enzyme activity is increased in newborn infants with respiratory distress syndrome and chronic alveolar hypoxia. Chronic hypoxic pulmonary hypertension is attenuated by angiotensin II receptor 1 (AT1) blockade in adult animals. To test whether angiotensin II (AT) is one of the mediators in the acute hypoxic pulmonary hypertension in newborn animals, 8 unanesthetized chronically instrumented piglets (mean ± SD; age, 6.5 ± 1.8 days; weight, 2181 ± 493 g) were randomly assigned to receive saline as a placebo solution (P) or AT1 antagonist, Losartan (L), in a crossover study design, with at least 48 hours interval between the first and the second study. Pulmonary artery (Pap), wedge (Pwp), systemic arterial (Psa) and right atrial (Rap) pressures, cardiac output (CO), pulmonary (PVR) and systemic (SVR) vascular resistances, and arterial blood gases were obtained in normoxia, before and during P or L infusion (6 mg/kg as a bolus, followed by 3 mg/kg/h), and during 6 hours of hypoxia (FiO2 = 0.11). Cardiac output was measured by thermodilution technique. Data were analyzed by repeated measures analysis of variance. Results (mean ± SD) are as follows: (Table)
Camelo, J., Hehre, D., Devia, C. et al. Role of Angiotensin II Receptor Blockade on Hypoxic Pulmonary Hypertension in Newborn Piglets.
Pediatr Res45, 297 (1999). https://doi.org/10.1203/00006450-199904020-01766