Response of the kidney to furosemide. I. Effects of salt intake and renal compensation

Christopher S. Wilcox, William E. Mitch, Ralph A. Kelly, Karl Skorecki, Timothy W. Meyer, Paul A. Friedman, Paul F. Souney

Research output: Contribution to journalArticlepeer-review

207 Scopus citations

Abstract

We investigated the effects of varying salt intake on five factors that could affect sodium balance during furosemide (F) administration: the quantity of F reaching the renal tubules; the magnitude of the acute natriuresis; Na+ excretion in the period after the acute diuresis; diuretic tolerance; and changes in plasma aldosterone. Six normal subjects were given F (40 mg day-1) for 3 days after equilibration to Na+ intakes of 20 mmol day-1 (low salt, LS) and 270 mmol day-1 (high salt, HS). Salt intake did not modify F excretion. Salt restriction reduced the short-term natriuretic response to F, led to diuretic tolerance, and potentiated the F-induced rise in plasma aldosterone. There was a progressive diminution in the quantity of Na+ excreted per unit of F excreted during LS. In spite of this, cumulative Na+ balance was negative only during LS because of a compensatory increase in Na+ reabsorption in the period between diuretic doses. During HS, this compensation exactly matched the short-term loss of Na+ produced by F, leading to neutral Na+ balance. During LS, the acute natriuresis exceeded the daily Na+ intake, so that, despite the renal compensation, Na+ balance was negative. In conclusion, salt restriction impairs the short-term natriuretic response to F and leads to diuretic tolerance. However, homeostatic mechanisms activated by the diuretic can maintain Na+ balance even in subjects without a disease causing Na+ retention, unless dietary salt is restricted.

Original languageEnglish
Pages (from-to)450-458
Number of pages9
JournalTranslational Research
Volume102
Issue number3
StatePublished - Sep 1983
Externally publishedYes

Fingerprint

Dive into the research topics of 'Response of the kidney to furosemide. I. Effects of salt intake and renal compensation'. Together they form a unique fingerprint.

Cite this