retinol-acetate and Respiratory-Distress-Syndrome--Newborn

Chronic lung disease (CLD) is a major cause of long-term morbidity in extremely LBW infants with respiratory distress syndrome. Parenteral vitamin A administration decreases the risk of CLD. We tested the hypothesis that intratracheal vitamin A administration with surfactant is systemically bioavailable without interfering with the functional properties of exogenous surfactant. Newborn piglets were ventilated with 100% FiO2 and sequential saline lavage induced respiratory distress syndrome. During lung injury induction, ventilator changes were allowed, but none were made following treatment allocation. Animals were assigned by chance in a blinded control trial to three groups: I=control; II=surfactant; III=surfactant+vitamin A. Hemodynamics, lung mechanics, and blood gases were measured following instrumentation, pre- and posttreatment for 4 h, at which time the liver was sampled for retinol determination. All parameters improved in animals receiving surfactant. A significant interaction existed between time and group for PaO2 and alveolar-arterial oxygen difference (A-aDO2). Hepatic levels of retinol were higher (p<0.001) in animals receiving retinyl acetate. Intratracheal administration of surfactant+vitamin A did not alter the beneficial effects of surfactant on lung compliance and gas exchange. Intratracheal Vitamin A was associated with rapid hepatic uptake. Further studies are warranted.

Topics: Administration, Inhalation; Animals; Animals, Newborn; Biological Availability; Disease Models, Animal; Diterpenes; Drug Combinations; Hemodynamics; Humans; Infant, Newborn; Intubation, Intratracheal; Liver; Lung; Lung Compliance; Oxygen; Pulmonary Gas Exchange; Pulmonary Surfactants; Respiratory Distress Syndrome, Newborn; Retinyl Esters; Swine; Time Factors; Vitamin A; Vitamins