Combined effects of low-dose oral spironolactone and captopril therapy in a rat model of spontaneous hypertension and heart failure

Atsushi Kambara, Bethany J. Holycross, Peter Wung, Brandon Schanbacher, Sarbani Ghosh, Sylvia A. McCune, John A. Bauer, Pawel Kwiatkowski

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

The effects of low-dose oral spironolactone (SPIRO) in a rat model of hypertensive heart failure (spontaneously hypertensive heart failure rat) were compared with its effects when combined with captopril (CAP). Twenty-six spontaneously rats with hypertensive heart failure were treated with either placebo (CON), SPIRO (20 mg/kg/d by mouth), CAP (100 mg/kg/d by mouth), or both SPIRO and CAP for 12 weeks. This dose of oral SPIRO did not affect blood pressure, left ventricular end-diastolic diameter, left ventricular ejection fraction, plasma atrial natriuretic peptide concentration, or cardiac fibrosis; however, in combination with CAP, it exerted a significant depressor effect after 12 weeks of treatment that was accompanied by increased urine output and decreased urinary protein excretion. These effects were significantly greater than those with CAP treatment alone. A significant increase in plasma aldosterone level was observed only in CON (174 ± 21%). These data suggest that the addition of low-dose SPIRO to angiotensin I-converting enzyme inhibitor treatment may prevent progression into end-stage congestive heart failure through synergistic effects on diuresis and renoprotection.

Original languageEnglish
Pages (from-to)830-837
Number of pages8
JournalJournal of Cardiovascular Pharmacology
Volume41
Issue number6
DOIs
StatePublished - Jun 1 2003

Keywords

  • ACE inhibitor
  • Diuresis
  • Heart failure
  • Hypertension
  • Spironolactone
  • Urinary protein

ASJC Scopus subject areas

  • Pharmacology
  • Cardiology and Cardiovascular Medicine

Fingerprint

Dive into the research topics of 'Combined effects of low-dose oral spironolactone and captopril therapy in a rat model of spontaneous hypertension and heart failure'. Together they form a unique fingerprint.

Cite this