Diuretic and natriuretic effects of nifedipine in healthy persons.

1. We have studied the diuretic and natriuretic effects and the tubular site of action of nifedipine using free water clearance (CH2O) and lithium clearance. 2. We have compared the effects of nifedipine (10 mg p.o.) with those of placebo and of frusemide (40 mg p.o.) in seven healthy volunteers during maximal water diuresis. 3. Compared with placebo, nifedipine caused a significant rise in urinary flow rate and CH2O, paralleled by significant increases in fractional excretion of sodium and lithium. The rise in sodium excretion was not accompanied by an increase in potassium excretion. 4. Frusemide caused increases in sodium and lithium excretion, comparable with the effects seen after nifedipine. CH2O did not change however. 5. Our study demonstrates that nifedipine has a clear diuretic and natriuretic effect in healthy volunteers, which is predominantly established by interference with proximal tubular sodium reabsorption. Lithium clearance did not allow us to differentiate between nifedipine and frusemide effects, thus questioning the reliability of lithium as a marker of proximal tubular sodium reabsorption.

[1]  T. Nagao,et al.  Calcium entry blockers: antihypertensive and natriuretic effects in experimental animals. , 1985, The American journal of cardiology.

[2]  A. Greenberg,et al.  Renal hemodynamic and tubular transport effects of nitrendipine. , 1985, The Journal of laboratory and clinical medicine.

[3]  C. Roberts,et al.  The natriuresis following oral administration of the calcium antagonists--nifedipine and nitrendipine. , 1985, British journal of clinical pharmacology.

[4]  A. Zanchetti,et al.  Natriuretic effect of calcium antagonists. , 1985, Journal of cardiovascular pharmacology.

[5]  G. G. Geyskes,et al.  Antihypertensive and renal effects of nicardipine. , 1984, British journal of clinical pharmacology.

[6]  G. Dibona,et al.  Renal tubular site of action of felodipine. , 1984, The Journal of pharmacology and experimental therapeutics.

[7]  K. Thomsen Lithium clearance: a new method for determining proximal and distal tubular reabsorption of sodium and water. , 1984, Nephron.

[8]  B. Brown,et al.  Renal effects of methoxyverapamil in anesthetized rats. , 1983, The Journal of pharmacology and experimental therapeutics.

[9]  K. Miura,et al.  Effects of the Calcium Antagonist Nicardipine on Renal Function and Renin Release in Dogs , 1983, Journal of cardiovascular pharmacology.

[10]  J. Puschett Sites and Mechanisms of Action of Diuretics in the Kidney , 1981, Journal of clinical pharmacology.

[11]  F. S. Wright,et al.  Luminal influences on potassium secretion: sodium concentration and fluid flow rate. , 1979, The American journal of physiology.

[12]  T. H. Steele,et al.  Pharmacological characterization of lithium reabsorption in the rat. , 1976, The Journal of pharmacology and experimental therapeutics.

[13]  M. A. Manuel,et al.  Renal lithium reabsorption in man: physiologic and pharmacologic determinants , 1975, The American journal of the medical sciences.

[14]  G. Giebisch,et al.  Effects of flow rate and potassium intake on distal tubular potassium transfer. , 1975, The American journal of physiology.

[15]  K. Ikezawa,et al.  Studies on a new 1,5-benzothiazepine derivative (CRD-401) VI. Effects on renal blood flow and renal function. , 1974, Japanese journal of pharmacology.

[16]  R. Jamison,et al.  A micropuncture study of collecting tubule function in rats with hereditary diabetes insipidus. , 1971, The Journal of clinical investigation.

[17]  F. S. Wright,et al.  An inhibitory effect of furosemide on sodium reabsorption by the proximal tubule of the rat nephron. , 1969, The Journal of clinical investigation.

[18]  R. Berliner,et al.  Permeability of the loop of Henle, vasa recta, and collecting duct to water, urea, and sodium. , 1968, The American journal of physiology.

[19]  J. Puschett,et al.  The acute effects of furosemide on acid and electrolyte excretion in man. , 1968, The Journal of laboratory and clinical medicine.