We examined the effects of N(G)-nitro-L-arginine (L-NNA) on isolated r
abbit afferent arterioles to confirm that nitric oxide is released at
the resistance vessel level in the kidney. We microdissected the super
ficial afferent arterioles from the kidneys of New Zealand White rabbi
ts. Each afferent arteriole was cannulated with a micropipette system,
and the intraluminal pressure was set at 80 mmHg. By our methods, we
found that norepinephrine (NE) decreased the lumen diameter of the aff
erent arterioles in a dose-dependent manner, and acetylcholine increas
ed the lumen diameter of NE-constricted afferent arterioles. L-NNA (10
(-4) M) gradually decreased the lumen diameter of afferent arterioles
from 21.5 +/- 0.9 to 18.6 +/- 0.9 mum in 20 min, but N(G)-nitro-D-argi
nine (10(-4) M) did not affect them (from 21.8 +/- 1.3 to 21.8 +/- 1.5
mum). L-Arginine (10(-2) M) restored the lumen diameter of L-NNA-cont
racted afferent arterioles to the control levels. These findings indic
ate that the isolated afferent arteriole has the ability to release or
to synthesize and release nitric oxide under basal conditions and tha
t this basal release of nitric oxide plays an important role in the ba
sal tone of the afferent arteriole.