The effects of two classes of phospholipids (PL) on renal function hav
e been studied. Bolus injections of 1 ng (10 pmol) of lysophosphatidyl
choline (LPC) caused natriuresis and diuresis in rats. Natriuretic act
ivity was eliminated by substituting unsaturated bonds in the 1-acyl g
roup and by removing the choline group on the sn-3 position. Natriuret
ic activity was not affected by substitution of 1-alkyl for 1-acyl gro
ups. In the dog, LPC was natriuretic when given as a bolus of 3.0 mug/
kg or as a constant infusion at 5 ng/kg/min. To explore further the ef
fect of alkyl PLs on renal function, a series of studies with platelet
activating factor (PAF) was performed. PAF injected directly into the
renal artery (IR) in bolus doses of 0.5-10 ng/kg caused renal vasodil
ation that was blocked by a specific PAF receptor antagonist. This eff
ect was not due to release of vasodilatory eicosanoids, dopamine, or n
itric oxide (NO). PAF given IR as a continuous infusion at 2.5 ng/kg/m
in attenuated the renal vasoconstrictor effects of angiotensin II and
norepinephrine but not vasopressin. This effect to attenuate vasoconst
riction was blocked by the NO inhibitor N-monomethyl-L-arginine. These
studies using picomolar amounts of PL suggest a physiologic role for
these compounds in control of renal function.