This proposal is directed toward improving our understanding of factors associated with neonatal lung injury and its long term clinical consequences. The component projects will examine the basis of acute lung injury as well as the sequence of injury that result in long term structural and functional alterations of the airway. The Center will include 6 major projects in addition to defined cores for administrative and programmatic needs of the Center. Specific projects are: 1) Neonatal Lung Matrix Drives Lung Repair. This study will define the influence of oxidant injury on lung epithelial basement membrane matrix interactions; 2) Alveolar Epithelial Differentiation in Oxidant Injury. This study will examine the influence of oxidant injury on Na+/K+ ATPase and gammaglutamyltransferase in lung; 3) Relationship Between Stress Proteins and Antioxidants in Hyperoxia. The heat shock response has been shown to be important in a variety of systems involved in injury and repair. We will examine heat shock proteins in relationship to endogenous antioxidant mechanisms following hyperoxic insult; 4) Regulation of Surfactant Phospholipid Metabolism in Injured Adult and Developing Lungs. This project will examine surfactant phospholipid synthesis in different populations of type II cells following silica induced lung injury; 5) The Influence of Butyrate Acid on SP-A Gene Transcription. This project will study the response of lung to a specific biochemical insult associated with alterations in gene expression; 6) Energetics of Breathing in Infants with Chronic Lung Disease. In this project, we will study alterations in lung work, respiratory efficiency and energy expenditure in infants with BPD who represent the final common pathway of acute lung injury. The SCOR will include 2 Cores which will provide support for the programmatic, educational, and oversight components as well as biostatistical support and a shared instrument facility. A shared morphology and electron microscopy core will provide support for the component laboratory projects. The interactions and shared knowledge provided through the Center will lead to a better understanding of the events underlying lung injury that will be essential before rational strategies for prevention can be rigorously developed and tested.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
1P50HL046488-01
Application #
3106916
Study Section
Special Emphasis Panel (SRC (MA))
Project Start
1991-12-30
Project End
1996-11-30
Budget Start
1991-12-30
Budget End
1992-11-30
Support Year
1
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Sherman, Aurora M; Shumaker, Sally A; Kancler, Cynthia et al. (2003) Baseline health-related quality of life in postmenopausal women with coronary heart disease: the Estrogen Replacement and Atherosclerosis (ERA) trial. J Womens Health (Larchmt) 12:351-62
Herrington, David M; Howard, Timothy D; Hawkins, Gregory A et al. (2002) Estrogen-receptor polymorphisms and effects of estrogen replacement on high-density lipoprotein cholesterol in women with coronary disease. N Engl J Med 346:967-74
Seres, T; Knickelbein, R G; Warshaw, J B et al. (2000) The phagocytosis-associated respiratory burst in human monocytes is associated with increased uptake of glutathione. J Immunol 165:3333-40
Galal, M W; Habib, R H; Jaeger, D D et al. (1998) Effects of rate and amplitude of breathing on respiratory system elastance and resistance during growth of healthy children. Pediatr Pulmonol 25:270-7
Jacobs, H C; Bogue, C W; Pinter, E et al. (1998) Fetal lung mRNA levels of Hox genes are differentially altered by maternal diabetes and butyrate in rats. Pediatr Res 44:99-104
Viviano, C J; Rooney, S A (1997) Early increase in expression of surfactant protein A gene in type II cells from silica-treated rats. Am J Physiol 273:L395-400
Knickelbein, R G; Seres, T; Lam, G et al. (1997) Characterization of multiple cysteine and cystine transporters in rat alveolar type II cells. Am J Physiol 273:L1147-55
Peters, J K; Lister, G; Nadel, E R et al. (1997) Venous and arterial reflex responses to positive-pressure breathing and lower body negative pressure. J Appl Physiol 82:1889-96
Ingbar, D H; Duvick, S; Savick, S K et al. (1997) Developmental changes of fetal rat lung Na-K-ATPase after maternal treatment with dexamethasone. Am J Physiol 272:L665-72
Bogue, C W; Jacobs, H C; Dynia, D W et al. (1996) Retinoic acid increases surfactant protein mRNA in fetal rat lung in culture. Am J Physiol 271:L862-8

Showing the most recent 10 out of 20 publications