The developmental changes in the activity of the renal kallikrein-kini
n system (KKS) are related to the hemodynamic changes occurring in the
neonatal kidney. In order to clarify the functional importance of the
renal KKS in the developing kidney, the effect of the bradykinin B2 r
eceptor antagonist HOE-140 was investigated in newborn rabbits. Effect
ive blockade of bradykinin effect by HOE-140 was demonstrated in 10 ra
bbits. In 10 additional animals the subcutaneous injection of 300 mu g
/kg HOE-140 resulted in an increase in renal vascular resistance with
a consequent decrease in renal blood flow. Glomerular filtration rate
did not change significantly, while the filtration fraction rose, indi
cating preferential efferent arteriolar constriction. Urine flow rate
increased as well as the fractional excretion of potassium. No change
in sodium excretion was observed. The present data suggest a regulator
y role for the renal KKS in the immature kidney under basal conditions
. By inducing predominant efferent arteriolar vasodilation, the KKS ap
pears to play a key role in regulating the neonatal glomerular microci
rculation. This is in sharp contrast with the mature kidney, where the
KKS predominantly acts on tubular function as a diuretic-natriuretic
factor.