This application is for 2 years of continued support of this Pulmonary Vascular SCOR grant entitled """"""""The Pathophysiology of Pulmonary Edema,"""""""" which includes multidisciplinary clinical and basic research projects concerned with two important clinical problems: pulmonary edema and pleural effusion. The objectives are to obtain new knowledge about the pathophysiology of liquid and protein exchange in the lungs and pleural spaces of experimental animals and man, and to use this knowledge to improve the diagnosis, treatment and prevention of pulmonary edema and pleural effusion in patients. To achieve these objectives, there are three research components and an administrative core unit. The key specific aims of the scientific projects are as follows: A-1: to develop and apply physiologic and biochemical tests that will identify from among the large number of patients at risk and who might have sustained acute lung injury, those who are actually destined to acquire clinical manifestations of pulmonary parenchymal damage, especially the severe pulmonary complication of sepsis called the Adult Respiratory Distress Syndrome; B-2: To examine the roles played by recently recognized circulating substances, cytokines and adhesion receptors, in the pathogenesis of certain forms of acute lung injury in sheep characterized by increased permeability pulmonary edema, especially that caused by infusions of endotoxin and live bacteria; and B- 3: to quantify the turnover of pulmonary liquid and protein in the lung and pleural space to obtain a more complete understanding of pulmonary liquid and protein exchange in health and disease. As documented in the supporting documents, considerable progress has been made during the 4 years of the present award, and the proposed projects represent logical extensions of the work already carried out by a group of investigators with a long tradition of successful interaction and productivity.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
2P50HL019155-16
Application #
3106550
Study Section
Special Emphasis Panel (SRC (MA))
Project Start
1976-12-01
Project End
1993-11-30
Budget Start
1991-12-17
Budget End
1992-11-30
Support Year
16
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Pittet, J F; Wiener-Kronish, J P; Serikov, V et al. (1995) Resistance of the alveolar epithelium to injury from septic shock in sheep. Am J Respir Crit Care Med 151:1093-100
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Folkesson, H G; Matthay, M A; Hebert, C A et al. (1995) Acid aspiration-induced lung injury in rabbits is mediated by interleukin-8-dependent mechanisms. J Clin Invest 96:107-16
Schnapp, L M; Chin, D P; Szaflarski, N et al. (1995) Frequency and importance of barotrauma in 100 patients with acute lung injury. Crit Care Med 23:272-8
McElroy, M C; Pittet, J F; Hashimoto, S et al. (1995) A type I cell-specific protein is a biochemical marker of epithelial injury in a rat model of pneumonia. Am J Physiol 268:L181-6
Pittet, J F; Wiener-Kronish, J P; McElroy, M C et al. (1994) Stimulation of lung epithelial liquid clearance by endogenous release of catecholamines in septic shock in anesthetized rats. J Clin Invest 94:663-71
Folkesson, H G; Kheradmand, F; Matthay, M A (1994) The effect of salt water on alveolar epithelial barrier function. Am J Respir Crit Care Med 150:1555-63
Boylan, A M; Hebert, C A; Sadick, M et al. (1994) Interleukin-8 is a major component of pleural liquid chemotactic activity in a rabbit model of endotoxin pleurisy. Am J Physiol 267:L137-44

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