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1 Perinatal Research
Laboratories, Departments of Obstetrics and Gynecology and Pediatrics,
University of California, Los Angeles School of Medicine, Harbor-UCLA
Medical Center, Torrance, California 90502;
2 Department of Pediatrics,
Abnormalities of premature newborn
adaptation after preterm birth result in significant perinatal
mortality and morbidity. We assessed the effects of short-term (24 h)
fetal betamethasone exposure on preterm newborn baboon pulmonary and
cardiovascular regulation and renal sodium handling during the first 24 h after birth. Male fetal baboons
(Papio) (124-day gestation, term 185 days) received ultrasound-guided intramuscular injections of saline (n = 5) or betamethasone (0.5 mg/kg;
n = 5). Fetuses were cesarean delivered 24 h later, treated with 100 mg/kg surfactant, and ventilated by adjusting peak inspiratory pressures to maintain
PCO2 values of 35-50 mmHg for 24 h. Betamethasone- vs. saline-treated mean ± SE newborn body weights
(0.45 ± 0.02 vs. 0.41 ± 0.01 kg) were similar. Although
prenatal betamethasone did not affect postnatal lung function
(PCO2, arterial/alveolar
O2 gradient, or dynamic
compliance), plasma hormone (cortisol or thyroxine), or catecholamine
levels, mean arterial pressure (25 ± 1 vs. 32 ± 1 mmHg), plasma
sodium concentration (132 ± 2 vs. 138 ± 1 meq/l), glomerular
filtration rate (0.07 ± 0.02 vs. 0.16 ± 0.02 ml · min
1 · kg
1),
and renal total sodium reabsorption (1.5 ± 0.5 vs. 16.0 ± 3.0 µeq · min
1 · kg
1)
values were significantly lower in saline-treated than in
betamethasone-treated newborns at 24 h. We conclude that despite the
fact that there are no pulmonary and endocrine effects, antenatal
glucocorticoid exposure alters premature newborn baboon vascular and
renal glomerular function and improves sodium reabsorption after
preterm delivery.
lung; kidney; blood pressure; betamethasone
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