This Hypertension SCOR will utilize a multidisciplinary approach to study the etiology, therapy, and complications of hypertension and the role which humoral factors factors play in these processes. One important objective will be to delineate the role of the renin-angiotensin system in experimental and clinical hypertension and the clinical usefulness of long-term angiotensin blockade. We plan to characterize the importance of sodium and volume factors in hypertensive states and to study their interaction with peripheral sympathetic activity, vasoactive hormones, cardiovascular function, and the renal kallikrein-kinin system. We will attempt to identify new mineralocorticoid hormones that could influence the development of hypertension in man and to determine the cause of low renin hypertension. We will study human alpha and beta adrenergic receptor activity in model system using circulating blood cells, and will assess the relationship of such receptor binding to plasma catecholamines, adrenergic responses, and antihypertensive therapy. We also will examine the effects of tyrosine and other amino acids on blood pressure and sympathetic activity in order to develop new therapeutic approaches for both hypertension and orthostatic hypotension. The influence of hypertension and its therapy on vascular and cardiac complications also will be investigated. These studies will focus in part on the mechanisms by which hypertension induces vascular injury in both arteries and arterioles and the effects of various treatments on the prevention on reversal of this process. We also will characterize the influence of hypertension and its treatment on the metabolism of arteries and cerebral micro-vessels and will study in detail the properties and regulation of angiotensin I converting enzyme. Treatment of congesive heart failure by angiotensin I blockade will be studied both in conscious dogs and man. Finally, we hope to clarify the role of the renin-angiotensin system in the regulation of regional and systemic vascular resistance in experimental animals with coronary occlusion and in patients with peripheral vascular disease. These studies should provide important insights into the pathogenesis and complications of hypertension and lead to improved approaches for its prevention and therapy.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
5P50HL018318-10
Application #
3106518
Study Section
(SRC)
Project Start
1975-12-01
Project End
1985-11-30
Budget Start
1984-12-01
Budget End
1985-11-30
Support Year
10
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Boston University
Department
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
Beasley, D; Schwartz, J H; Brenner, B M (1991) Interleukin 1 induces prolonged L-arginine-dependent cyclic guanosine monophosphate and nitrite production in rat vascular smooth muscle cells. J Clin Invest 87:602-8
Schwartz, J H; Bengele, H H; McNamara, E R et al. (1990) Vasopressin-enhanced urea transport by rat inner medullary collecting duct cells in culture. Cell Tissue Kinet 23:487-93
Griffing, G T; Wilson, T E; Melby, J C (1990) Alterations in aldosterone secretion and metabolism in low renin hypertension. J Clin Endocrinol Metab 71:1454-60
Slotki, I N; Schwartz, J H; Alexander, E A (1990) Na(+)-H+ exchange is stimulated by protein kinase C activation in inner medullary collecting duct cells. Am J Physiol 259:F666-71
Brion, L P; Schwartz, J H; Zavilowitz, B J et al. (1990) Differentiation of proton-pumping activity in cultured renal inner medullary collecting duct cells. Pediatr Nephrol 4:408-14
Siskind, M S; Alexander, E A; Schwartz, J H (1990) Regulation of cGMP production by intracellular alkalinization in cultured rat inner medullary collecting duct cells. Biochem Biophys Res Commun 170:860-6
Slotki, I N; Schwartz, J H; Alexander, E A (1989) Effect of increases in cytosolic Ca2+ on inner medullary collecting duct cell pH. Am J Physiol 257:F210-7
Griffing, G T; Holbrook, M M; Bencsath, F A et al. (1989) Renal 21-hydroxylation of 19-hydroxy-progesterone to 19-hydroxy-deoxycorticosterone. J Steroid Biochem 33:895-8
Brion, L P; Schwartz, J H; Lachman, H M et al. (1989) Development of H+ secretion by cultured renal inner medullary collecting duct cells. Am J Physiol 257:F486-501
Griffing, G T; Holbrook, M; Melby, J C et al. (1989) 19-Hydroxylase inhibition of adrenal mitochondrial P450 11 beta/18/19-hydroxylase by a suicide inhibitor. Am J Med Sci 298:83-8

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