TY - JOUR
T1 - Combined effects of low-dose oral spironolactone and captopril therapy in a rat model of spontaneous hypertension and heart failure
AU - Kambara, Atsushi
AU - Holycross, Bethany J.
AU - Wung, Peter
AU - Schanbacher, Brandon
AU - Ghosh, Sarbani
AU - McCune, Sylvia A.
AU - Bauer, John A.
AU - Kwiatkowski, Pawel
PY - 2003/6/1
Y1 - 2003/6/1
N2 - 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.
AB - 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.
KW - ACE inhibitor
KW - Diuresis
KW - Heart failure
KW - Hypertension
KW - Spironolactone
KW - Urinary protein
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UR - http://www.scopus.com/inward/citedby.url?scp=0037780761&partnerID=8YFLogxK
U2 - 10.1097/00005344-200306000-00002
DO - 10.1097/00005344-200306000-00002
M3 - Article
C2 - 12775959
AN - SCOPUS:0037780761
SN - 0160-2446
VL - 41
SP - 830
EP - 837
JO - Journal of Cardiovascular Pharmacology
JF - Journal of Cardiovascular Pharmacology
IS - 6
ER -