The respiratory distress syndrome (RDS) remains a major cause of morbidity and mortality for premature infants. While inadequate surfactant pools at birth precipitate the pathophysiology of RDS, very little is known about surfactant phospholipid metabolism during RDS and the effects of secondary pathophysiologic events on surfactant metabolism and function. Surfactant replacement therapy can effectively treat RDS as demonstrated in both animals and in early clinical trials; however, possible effects of that replacement therapy on endogenous surfactant metabolic pathways in the premature remain unexplored. This grant will combine biochemical and physiological studies of surfactant metabolism and function with measurements of pulmonary function such as the distribution of pulmonary blood flow, ventilation, and protein leak in the lungs of prematurely delivered and ventilated lambs with RDS. Surfactant metabolism (pool sizes, labeling kinetics, possible recycling), surfactant function (surface properties, aggregate sizes of surfactant within the airways, inhibitor), and the effect of treatment with natural sheep surfactant will be characterized. The permeability properties of the immature lung to preoteins and other large molecular weight molecules will be measured, and variables such as ventilation, surfactant treatment, and atelectasis that may affect the permeability will be studied. Other factors known to influence lung function in the premature such as birth asphyxia and the patent ductus arteriosus will be experimentally manipulated to better define the relationships between permeability changes and surfactant function. The experiments will provide quantitative measurements of multiple variables such that the relative importance of the different processes can be assessed. The overall goals are to establish an understanding of the relationships between surfactant function and metabolism and the pathophysiologic sequence of RDS, and to better characterize how exogenously administered surfactant affects the process.

Project Start
1979-04-01
Project End
1990-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
10
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Los Angeles County Harbor-UCLA Medical Center
Department
Type
DUNS #
City
Torrance
State
CA
Country
United States
Zip Code
90509
Hillman, Noah H; Gisslen, Tate; Polglase, Graeme R et al. (2014) Ventilation-induced increases in EGFR ligand mRNA are not altered by intra-amniotic LPS or ureaplasma in preterm lambs. PLoS One 9:e96087
Hillman, Noah H; Moss, Timothy J; Nitsos, Ilias et al. (2012) Moderate tidal volumes and oxygen exposure during initiation of ventilation in preterm fetal sheep. Pediatr Res 72:593-9
Pillow, J Jane; Musk, Gabrielle C; McLean, Carryn M et al. (2011) Variable ventilation improves ventilation and lung compliance in preterm lambs. Intensive Care Med 37:1352-9
Hillman, Noah H; Polglase, Graeme R; Pillow, J Jane et al. (2011) Inflammation and lung maturation from stretch injury in preterm fetal sheep. Am J Physiol Lung Cell Mol Physiol 300:L232-41
Hillman, Noah H; Nitsos, Ilias; Berry, Clare et al. (2011) Positive end-expiratory pressure and surfactant decrease lung injury during initiation of ventilation in fetal sheep. Am J Physiol Lung Cell Mol Physiol 301:L712-20
Hillman, Noah H; Kallapur, Suhas G; Pillow, J Jane et al. (2010) Airway injury from initiating ventilation in preterm sheep. Pediatr Res 67:60-5
Hillman, Noah H; Kallapur, Suhas G; Pillow, J Jane et al. (2010) Inhibitors of inflammation and endogenous surfactant pool size as modulators of lung injury with initiation of ventilation in preterm sheep. Respir Res 11:151
Kunzmann, Steffen; Glogger, Kerstin; Been, Jasper V et al. (2010) Thymic changes after chorioamnionitis induced by intraamniotic lipopolysaccharide in fetal sheep. Am J Obstet Gynecol 202:476.e1-9
Ball, Molly K; Hillman, Noah H; Kallapur, Suhas G et al. (2010) Body temperature effects on lung injury in ventilated preterm lambs. Resuscitation 81:749-54
Kramer, Boris W; Kallapur, Suhas G; Moss, Timothy J M et al. (2010) Modulation of fetal inflammatory response on exposure to lipopolysaccharide by chorioamnion, lung, or gut in sheep. Am J Obstet Gynecol 202:77.e1-9

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