EFFECTS OF CANRENONE ON BLOOD-PRESSURE IN RATS WITH REDUCED RENAL MASS

被引:41
作者
PAMNANI, MB
WHITEHORN, WV
CLOUGH, DL
HADDY, FJ
机构
[1] The Department of Physiology, Uniformed Services University of the Health Sciences, Bethesda, MD
关键词
Canrenone; Hypertension; Reduced renal mass;
D O I
10.1093/ajh/3.3.188
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Canrenone, a metabolic product of spironolactone, which competes with ouabain for binding to Na-K-ATPase at the digitalis receptor site and by itself inhibits Na-K-ATPase, was administered intramuscularly to reduced renal mass-saline drinking hypertensive and reduced renal mass-distilled water drinking normotensive rats for 8 days. Reduced renal mass-saline hypertension in the rat, is a low renin, volume expanded form of hypertension. Rats with this type of hypertension have been shown to have depressed arterial Na-K pump activity and increased Na-K pump inhibitory activity in their plasma. Canrenone treatment caused a progressive decrease in blood pressure in the hypertensive rats and this was associated with normalization of Na-K pump activity in arteries. Water and salt intake and excretion did not change. On the other hand, canrenone progressively increased blood pressure in the normotensive rats and this was associated with positive inotropy in isolated papillary muscles. These findings suggest that the depressed pump activity and the pump inhibitor play a role in reduced renal mass-saline hypertension in the rat and that the rise in blood pressure in the normotensive rats probably reflects canrenone's ability, by itself, to inhibit Na-K-ATPase. Am J Hypertens 1990;3:188-195. © 1990, American Journal of Hypertension, Ltd. All rights reserved.
引用
收藏
页码:188 / 195
页数:8
相关论文
共 34 条
[1]  
Huot S.J., Pamnani M.B., Clough D.L., Haddy F.J., The role of sodium intake, the Na+-K+ pump and a ouabain like humoral agent in the genesis of reduced renal mass hypertension, Am J Nephrol, 3, pp. 92-99, (1983)
[2]  
Huot S.J., Pamnani M.B., Clough D., Et al., Sodium-potassium pump activity in reduced renal mass hypertension, Hypertension, 5, pp. 194-1100, (1983)
[3]  
Pamnani M.B., Huot S.J., Buggy J., Et al., Demonstration of a humoral inhibitor of the Na+-K+ pump in some models of experimental hypertension, Hypertension, 3, pp. II96-II101, (1981)
[4]  
Ylitalo P., Hepp R., Oster P., Et al., Effects of varying sodium intake on blood pressure and renin-angiotensin system in subtotally nephrectomized rats, J Lab Clin Med, 88, pp. 807-816, (1976)
[5]  
Brace R.A., Anderson D.K., Chen W.T., Et al., Local effects of hypokalemia on coronary resistance and myocardial contractile force, Am J Physiol, 227, pp. 590-597, (1974)
[6]  
Vatner D.F., Higgins C.B., Franklin D., Braunwald E., Effects of digitalis glycoside on coronary and systemic dynamics in conscious dogs, Circ Res, 28, pp. 470-479, (1971)
[7]  
DeMots H.S., Rahimtoola S.H., McAnulty J.H., Porter G.A., Effects of ouabain on coronary and systemic vascular resistance and myocardial oxygen consumption in patients without heart failure, Am J Cardiol, 41, pp. 88-93, (1978)
[8]  
Haddy F.J., Scott J.B., Mechanisms of the acute pressor action of hypokalemia, hypomagnesemia, and hypoos- molality, Am Heart J, 85, pp. 655-661, (1973)
[9]  
Brender D., Vanhoutte P.M., Shepherd J.T., Potentiation of adrenergic venomotor responses in dogs by cardiac glycosides, Circ Res, 25, pp. 597-606, (1969)
[10]  
Ramsy L., Asbury M., Shelton J., Harrison I., Spironolactone and canrenoate-K: Relative potency steady state, Clin Pharmacol Ther, 21, pp. 602-609, (1977)