Postnatal estradiol up-regulates lung nitric oxide synthases and improves lung function in bronchopulmonary dysplasia.

McCurnin DC, Pierce RA, Willis BC, Chang LY, Yoder BA, Yuhanna IS, Ballard PL, Clyman RI, Waleh N, Maniscalco W, Crapo JD, Grubb PH, Shaul PW
Am J Respir Crit Care Med. 2009 179 (6): 492-500

PMID: 19151197 · PMCID: PMC2654978 · DOI:10.1164/rccm.200805-794OC

RATIONALE - Nitric oxide (NO) plays an important role in lung development and perinatal lung function, and pulmonary NO synthases (NOS) are decreased in bronchopulmonary dysplasia (BPD) following preterm birth. Fetal estradiol levels increase during late gestation and estradiol up-regulates NOS, suggesting that after preterm birth estradiol deprivation causes attenuated lung NOS resulting in impaired pulmonary function.

OBJECTIVE - To test the effects of postnatal estradiol administration in a primate model of BPD over 14 days after delivery at 125 days of gestation (term = 185 d).

METHODS - Cardiopulmonary function was assessed by echocardiography and whole body plethysmography. Lung morphometric and histopathologic analyses were performed, and NOS enzymatic activity and abundance were measured.

MEASUREMENTS AND MAIN RESULTS - Estradiol caused an increase in blood pressure and ductus arteriosus closure. Expiratory resistance and lung compliance were also improved, and this occurred before spontaneous ductal closure. Furthermore, both oxygenation and ventilation indices were improved with estradiol, and the changes in lung function and ventilatory support requirements persisted throughout the study period. Whereas estradiol had negligible effect on indicators of lung inflammation and on lung structure assessed after the initial 14 days of ventilatory support, it caused an increase in lung neuronal and endothelial NOS enzymatic activity.

CONCLUSIONS - In a primate model of BPD, postnatal estradiol treatment had favorable cardiovascular impact, enhanced pulmonary function, and lowered requirements for ventilatory support in association with an up-regulation of lung NOS. Estradiol may be an efficacious postnatal therapy to improve lung function and outcome in preterm infants.

MeSH Terms (25)

Animals Animals, Newborn Blood Pressure Bronchoalveolar Lavage Fluid Bronchopulmonary Dysplasia Disease Models, Animal Ductus Arteriosus Elastin Estradiol Estrogens Female Humans Infant, Newborn Lung Lung Compliance Male Nitric Oxide Synthase Oxygen Papio Pulmonary Surfactants Random Allocation Receptors, Estradiol Respiration, Artificial RNA, Messenger Up-Regulation

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