The renin-angiotensin-aldosterone systems and renal kallikrein and prostaglandins normally participate in the homeostatic regulation of electrolyte and acid-base composition, extracellular fluid volume and blood pressure. We are studying abnormalities of these hormonal systems in disorders of electrolyte and acid-base metabolims and hypertension in human beings. Aldosterone deficiency, usually occurring as a consequence of a primary deficiency of renin secretion (hyporenineumic hypoaldosteronism), is a common finding in patients with chronic renal insufficiency and an important cause of significant hyperkalemia and hyperchloremic metabolic acidosis. Studies under metabolic ward conditions with rigorous control of net potassium load and administration of pharmacologic agents (captopril, indomethasin) are utilized to define the relationship between the hormonal systems and maintenance of potassium and acid-base homeostasis. Studies of these hormonal systems are being conducted in patients with various hypokalemic syndromes due to renal potassium wasting and in normal subjects made hypokalemic by dietary potassium restriction. The effect of hypokalemia on solute transport in the diluting segment of the nephron and the effect of treatment with a """"""""potassium sparing"""""""" agent, amiloride, are also being evaluated in this study population. Studies ae being conducted in hypertensive disorders characterized by increased activity of the renin-angiotensin systems and/or adrenal mineralocorticoid hormones to define the pathogenic adnormalities and to determine optimal therapy for such patients. The relationship between extracellular fluid volume and the renal kallikrein and protaglandin systems in the pathogenesis of hypertension in patients with chronic renal insufficiency is also under investigation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL011046-19
Application #
3334406
Study Section
Cardiovascular and Pulmonary Research B Study Section (CVB)
Project Start
1977-01-01
Project End
1985-12-31
Budget Start
1985-01-01
Budget End
1985-12-31
Support Year
19
Fiscal Year
1985
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
Giacchetti, G; Sechi, L A; Griffin, C A et al. (2000) The tissue renin-angiotensin system in rats with fructose-induced hypertension: overexpression of type 1 angiotensin II receptor in adipose tissue. J Hypertens 18:695-702
Engler, M M; Schambelan, M; Engler, M B et al. (1998) Effects of dietary gamma-linolenic acid on blood pressure and adrenal angiotensin receptors in hypertensive rats. Proc Soc Exp Biol Med 218:234-7
Sechi, L A; Ceriello, A; Griffin, C A et al. (1997) Renal antioxidant enzyme mRNA levels are increased in rats with experimental diabetes mellitus. Diabetologia 40:23-9
Griffin, C A; Giacchetti, G; Schambelan, M et al. (1997) Ontogenic expression of renal and hepatic angiotensin II receptor genes in the rat. Nephron 76:103-10
Sechi, L A; Griffin, C A; Zingaro, L et al. (1997) Effects of angiotensin II on insulin receptor binding and mRNA levels in normal and diabetic rats. Diabetologia 40:770-7
Valentin, J P; Sechi, L A; Griffin, C A et al. (1997) The renin-angiotensin system and compensatory renal hypertrophy in the rat. Am J Hypertens 10:397-402
Sechi, L A; Griffin, C A; Giacchetti, G et al. (1996) Tissue-specific regulation of type 1 angiotensin II receptor mRNA levels in the rat. Hypertension 28:403-8
Sechi, L A; Griffin, C A; Giacchetti, G et al. (1996) Abnormalities of insulin receptors in spontaneously hypertensive rats. Hypertension 27:955-61
Sechi, L A; Valentin, J P; Griffin, C A et al. (1995) Receptors for atrial natriuretic peptide are decreased in the kidney of rats with streptozotocin-induced diabetes mellitus. J Clin Invest 95:2451-7
Schambelan, M (1994) Licorice ingestion and blood pressure regulating hormones. Steroids 59:127-30

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