Pf. Vos et al., EFFECTS OF ENALAPRIL ON RENAL SODIUM HANDLING IN HEALTHY-SUBJECTS ON LOW, INTERMEDIATE, AND HIGH SODIUM-INTAKE, Journal of cardiovascular pharmacology, 22(1), 1993, pp. 27-32
Angiotensin-converting enzyme (ACE) inhibitors have a modest natriuret
ic effect, but the responsible changes in tubular sodium (Na) handling
are not fully known. We therefore studied the effect of a single dose
of 20 mg enalapril on Na excretion in 8 healthy subjects, using lithi
um clearance and maximal water diuresis to analyze tubular Na handling
. Because the natriuretic effect may depend on the volume state, the s
ame subjects were studied during low (20 mmol Na/day), medium (200 mmo
l Na/day), and high (400 mmol Na/day) salt intake. Enalapril caused na
triuresis during the 20-mmol Na diet (from 51 +/- 9 to 81 +/- 14 mumol
/min, p < 0.05) and the 200-mmol Na diet (from 190 +/- 24 to 230 +/- 3
1 mumol/min, p < 0.05), but not during the 400-mmol Na diet. The incre
ase in Na excretion was not accompanied by consistent changes in glome
rular filtration rate (GFR), free water clearance data, maximal urine
flow, uric acid clearance, or lithium clearance. Instead, the increase
in Na excretion was positively related to the increase in Na concentr
ation in the maximally diluted urine (r = 0.75, p < 0.01). Regardless
of diet, enalapril reduced the filtration fraction, but a significant
increase in effective renal plasma flow was noted only during the 20-m
mol Na diet. The data suggest that a decrease in Na reabsorption in th
e diluting segment, perhaps related to renal vasodilatation, participa
tes in the natriuretic effect of ACE inhibition in humans.