The role of sodium depletion in hydrochlorothiazide-induced antidiuresis in Brattleboro rats with diabetes insipidus.

1. The mechanism of the antidiuretic effect of hydrochlorothiazide in diabetes insipidus was studied in anaesthetized Brattleboro rats with the hereditary hypothalamic form of the disease. 2. The antidiuresis caused by acute administration of hydrochlorothiazide followed an increase in sodium excretion and was associated with a significant fall in the plasma sodium concentration. There were concomitant falls in effective renal plasma flow and glomerular filtration rate. 3. When sodium depletion was prevented by adjusting the infusion of sodium chloride, the falls in plasma sodium concentration, effective renal plasma flow and glomerular filtration rate were abolished. Under these circumstances there was an increase in urine volume, which suggests that hydrochlorothiazide may inhibit fractional fluid reabsorption in the proximal convoluted tubule. 4. The results indicate that the antidiuresis caused by hydrochlorothiazide in diabetes insipidus results, at least in part, from falls in effective renal plasma flow and glomerular filtration rate. These in turn seem to be entirely secondary to the drug-induced sodium depletion.

[1]  S. Walter,et al.  Mechanism of the antidiuretic effect of hydrochlorothiazide in diabetes insipidus [proceedings]. , 1977, The Journal of physiology.

[2]  R. Kunau,et al.  Clarification of the site of action of chlorothiazide in the rat nephron. , 1975, The Journal of clinical investigation.

[3]  J. H. Stein,et al.  Segmental sodium reabsorption in rats with mild and severe volume depletion. , 1974, The American journal of physiology.

[4]  J. Puschett,et al.  Proximal tubular actions of metolazone and chlorothiazide. , 1973, The American journal of physiology.

[5]  R. Sutton,et al.  Micropuncture study of diuretic effects on sodium and calcium reabsorption in the dog nephron. , 1973, The Journal of clinical investigation.

[6]  M. Weiner,et al.  Accelerated reabsorption in the proximal tubule produced by volume depletion. , 1971, The Journal of clinical investigation.

[7]  J. R. Clapp,et al.  Distal sites of action of diuretic drugs in the dog nephron. , 1968, The American journal of physiology.

[8]  A. Lant,et al.  Localization of the site of action of oral diuretics in the human kidney. , 1967, Clinical science.

[9]  K. Thurau INFLUENCE OF SODIUM CONCENTRATION AT MACULA DENSA CELLS ON TUBULAR SODIUM LOAD * , 1966, Annals of the New York Academy of Sciences.

[10]  E. Skadhauge Studies of the antidiuresis induced by natrichloriuretic drugs in rats with diabetes insipidus. , 1966, Quarterly journal of experimental physiology and cognate medical sciences.

[11]  S. Friedman,et al.  SALT AND WATER DISTRIBUTION IN HEREDITARY AND IN INDUCED HYPOTHALAMIC DIABETES INSIPIDUS IN THE RAT , 1965 .

[12]  J. Gillenwater ANTIDIURETIC PROPERTIES OF CHLOROTHIAZIDE IN DIABETES INSIPIDUS DOGS. , 1965, Metabolism: clinical and experimental.

[13]  G. C. Kennedy,et al.  Electrolyte conservation during the treatment of diabetes insipidus with benzothiadiazines. , 1963, Quarterly journal of experimental physiology and cognate medical sciences.

[14]  J. Orloff,et al.  THE MECHANISM OF ANTIDIURESIS ASSOCIATED WITH THE ADMINISTRATION OF HYDROCHLOROTHIAZIDE TO PATIENTS WITH VASOPRESSIN-RESISTANT DIABETES INSIPIDUS. , 1962, The Journal of clinical investigation.

[15]  K. Beyer,et al.  Effect of hydrochlorothiazide on renal electrolyte gradient in glucose diuresis and experimental diabetes insipidus. , 1962, Journal of Pharmacology and Experimental Therapeutics.

[16]  P. Wood,et al.  The effect of diuretics on renal water excretion in diabetes insipidus. , 1961, Clinical science.

[17]  J. Crawford,et al.  Chlorothiazid in Diabetes Insipidus , 1959, Nature.