The major aim of this proposal is to evaluate the changes which occur in lung endothelial and epithelial permeability and vascular resistances as related to capillary pressures, following neutrophil activation, complement activation (ZAP), and platelet activating factor and paraquat challenges via the circulation. Pulmonary edema can result because capillaries are abnormally leaky to plasma proteins and/or capillary pressure is elevated. We selected these challenges because they produce intense vasoconstriction,, with the exception of platelet activating factor which relaxes rat pulmonary circulation, pulmonary edema, and in some cases damaged endothelium. We will evaluate the effects of antioxidants (e.g., superoxide dismutase, catalase, promethazine, and DPPD), alpha and beta adrenergenic compounds (e.g., norepinephrine, isoproterenol), acetylcholine, arachidonic acid system (thromboxane synthetase inhibitor), histamine blockers (benadryl and cimetidine) in isolated rat, dog and guinea pig lungs subjected to these challenges. We will measure the large and small arterial and, venous resistances and compliances, along with capillary pressures in normal and damaged lungs to determine how the various components of the alpha, beta H1, H2, and AA systems alter resistances and compliances in each compartment. In addition, we will also evaluate an important permeability parameter, the permeability surface area product using prenodal lymph draining an open-chested dog preparation to determine this membrane-solute parameter for 6 endogenous plasma proteins. Also, we will measure unidirectional albumin fluxes across the endothelial barrier in isolated lungs to determine if the flux is the same in both directions, and whether or not these fluxes are altered in hypoxia and different forms lung damage. Finally, we will evaluate the permeability properties of the alveolar membrane in lungs challenged with PMA, ZAP, platelet activating factor or paraquat to determine the role this important membrane plays in the development of pulmonary edema.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
4R37HL022549-16
Application #
3485781
Study Section
Special Emphasis Panel (NSS)
Project Start
1977-09-01
Project End
1997-08-31
Budget Start
1992-09-30
Budget End
1993-08-31
Support Year
16
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of South Alabama
Department
Type
Schools of Medicine
DUNS #
City
Mobile
State
AL
Country
United States
Zip Code
36688
Corboz, M R; Ballard, S T; Gao, H et al. (2000) Differential effects of furosemide on porcine bronchial arterial and airway smooth muscle. J Appl Physiol 89:1360-4
Khimenko, P L; Taylor, A E (1999) Segmental microvascular permeability in ischemia-reperfusion injury in rat lung. Am J Physiol 276:L958-60
Wilson, P S; Thompson, W J; Moore, T M et al. (1997) Vasoconstriction increases pulmonary nitric oxide synthesis and circulating cyclic GMP. J Surg Res 70:75-83
Inglis, S K; Corboz, M R; Taylor, A E et al. (1997) Effect of anion transport inhibition on mucus secretion by airway submucosal glands. Am J Physiol 272:L372-7
Inglis, S K; Corboz, M R; Taylor, A E et al. (1997) In situ visualization of bronchial submucosal glands and their secretory response to acetylcholine. Am J Physiol 272:L203-10
Corboz, M R; Ballard, S T; Inglis, S K et al. (1997) Dilatory effect of furosemide on rat tracheal arterioles and venules. Am J Respir Crit Care Med 156:478-83
Corboz, M R; Ballard, S T; Inglis, S K et al. (1996) Tracheal microvascular responses to beta-adrenergic stimulation in anesthetized rats. Am J Respir Crit Care Med 153:1093-7
Wilson, P S; Khimenko, P; Moore, T M et al. (1996) Perfusate viscosity and hematocrit determine pulmonary vascular responsiveness to NO synthase inhibitors. Am J Physiol 270:H1757-65
Inglis, S K; Corboz, M R; Taylor, A E et al. (1996) Regulation of ion transport across porcine distal bronchi. Am J Physiol 270:L289-97
Corboz, M R; Ballard, S T; Inglis, S K et al. (1996) Tracheal microvascular responses to inhibition of nitric oxide synthesis in anesthetized rats. Am J Respir Crit Care Med 154:1382-6

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