Circulation, Vol 90, 220-224, Copyright © 1994 by American Heart Association
JM Good, AJ Brady, FH Noormohamed, CM Oakley and JG Cleland
BACKGROUND: Contrary to expectation, most studies have demonstrated that
initiation of an angiotensin-converting enzyme (ACE) inhibitor in
conventional doses in patients with heart failure reduces the diuretic
efficacy of furosemide. Recently, it has been suggested that single low
doses (1 mg) but not high doses (25 mg) of captopril enhance furosemide-
induced diuresis. It is not known whether the interaction between diuretics
and ACE inhibitors are altered during long-term dosing. METHODS AND
RESULTS: Eight patients with heart failure treated with diuretics and ACE
inhibitors for at least 3 months were studied. All patients were
established on captopril 12.5 mg three times daily for 2 weeks before the
study. Sodium intake was fixed before the study, and usual medication was
withheld on study days. Intravenous furosemide was given on each of 2 study
days to maintain a moderate, constant diuresis. Renal plasma flow and
glomerular filtration rate (GFR) were determined using clearance
techniques, and urine was collected hourly over 4 hours. Captopril 12.5 mg
or placebo was given in a randomized, single-blind fashion at the end of
the first hour. Compared with placebo, captopril reduced plasma
concentrations of angiotensin II (23 +/- 18 versus 4 +/- 3 pg/ml 1 hour
after dosing, P < .02) and systolic (131 +/- 31 versus 122 +/- 29 mm Hg,
P < .01) and diastolic (74 +/- 15 versus 67 +/- 13 mm Hg, P < .05)
blood pressures. GFR fell (55 +/- 24 versus 51 +/- 22 mL/min, P < .02)
and effective renal plasma flow rose during the first (198 +/- 76 versus
231 +/- 49 mL/min) and second hours after dosing (185 +/- 69 versus 247 +/-
74 mL/min, P < .02). Similarly, urine volumes, in response to
furosemide, increased after captopril (238 +/- 90 versus 283 +/- 111 mL, P
< .05, and 245 +/- 78 versus 311 +/- 92 mL, P < .01, 1 and 2 hours
after dosing). Urinary electrolyte concentrations fell, but total urinary
sodium (22 +/- 7 versus 28 +/- 12 mmol/hr, P < .01) and chloride (20 +/-
6 versus 25 +/- 11 mmol/hr, P < .05) excretion increased in the 2 hours
after dosing, as did fractional excretion of sodium (urinary sodium/urinary
creatinine) (61 +/- 27 versus 75 +/- 36 mmol/mumol, P < .01).
CONCLUSIONS: Intense although transient ACE inhibition with captopril
enhances the diuretic effects of furosemide during long-term ACE
inhibition.
ARTICLES
Effect of intense angiotensin II suppression on the diuretic response to furosemide during chronic ACE inhibition
Royal Postgraduate Medical School, Hammersmith Hospital, London.
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