In the biochemistry and physiology of the renin-angiotensin system will be examined in vitro and in vivo in experimental animals and in man in relation to circulatory homeostasis. The program will focus on two major areas: the action and regulation of angiotensin II (AII) metabolism in vivo. In pursuit of the former goal, we will perform detailed studies of the mechanism of action of converting enzyme and of possible disorders of and physiologic regulatory mechanisms for converting enzyme in man and in animal models. The latter will include acute and chronic hypoxia and alterations in sodium intake and posture. We will attempt to produce animal models of converting enzyme insufficiency by inducing oxygen toxicity in the rat lung and by injecting histamine depleting substances into the pulmonary circulation of the rat. Simultaneous measurements of pulmonary and plasma converting enzyme activity will be made in order to make a quantitative assessment of the contribution of the lung to the pool of circulating converting enzyme. We will search for evidence of antiotensin conversion in the brush border of the proximal tubule in order to elucidate the problem of the intrarenal origin of angiotensin II. Studies of angiotensin II metabolism, including sites, enzymatic mechanisms and functional roles of metabolites, will be performed. To achieve this goal we will investigate the regulation of AI conversion and AII metabolism in the kidney of dogs which have been maintained on diets of high or low sodium intake, which are expected to produce chronic alterations in renal hemodynamics and possibly in renal angiotensinase activity. Further, we will examine the hypothesis that the kidney distal to a stenosed renal artery has a diminished ability to remove AII from the circulation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL022544-08
Application #
3336924
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Project Start
1979-08-01
Project End
1987-07-31
Budget Start
1985-08-01
Budget End
1987-07-31
Support Year
8
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
Overall Medical
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Zhu, S T; Chen, Y F; Wyss, J M et al. (1996) Atrial natriuretic peptide blunts arterial baroreflex in spontaneously hypertensive rats. Hypertension 27:297-302
Meng, Q C; Durand, J; Chen, Y F et al. (1993) Simplified method for quantitation of angiotensin peptides in tissue. J Chromatogr 614:19-25
Wyss, J M; Mozaffari, M S; St John, P L et al. (1993) Cyclosporine-induced nephrotoxicity in deoxycorticosterone-NaCl treated rats. Int J Exp Pathol 74:615-26
Lipke, D W; McCarthy, K J; Elton, T S et al. (1993) Coarctation induces alterations in basement membranes in the cardiovascular system. Hypertension 22:743-53
Nakamura, Y; Calhoun, D A; Chen, Y F et al. (1993) Excitatory sympathetic reflex in NaCl-sensitive spontaneously hypertensive rats. Hypertension 22:285-91
Wyss, J M; Oparil, S; Sripairojthikoon, W (1992) Neuronal control of the kidney: contribution to hypertension. Can J Physiol Pharmacol 70:759-70
Contreras, R J; Oparil, S (1992) Sex difference in blood pressure of spontaneously hypertensive rats influenced by perinatal NaCl exposure. Physiol Behav 51:449-55
Jin, H; Mathews, C; Chen, Y F et al. (1992) Effects of acute and chronic blockade of neutral endopeptidase with Sch 34826 on NaCl-sensitive hypertension in spontaneously hypertensive rats. Am J Hypertens 5:210-8
Wyss, J M; Van Groen, T (1992) Early breakdown of dendritic bundles in the retrosplenial granular cortex of hypertensive rats: prevention by antihypertensive therapy. Cereb Cortex 2:468-76
Chen, Y F; Naftilan, A J; Oparil, S (1992) Androgen-dependent angiotensinogen and renin messenger RNA expression in hypertensive rats. Hypertension 19:456-63

Showing the most recent 10 out of 91 publications