The function of the neuronal isoform of nitric oxide synthase (nNOS) was st
udied by comparing the effects of the specific nNOS blocker 7-nitro indazol
e monosodium salt (7-NINA) with that of the general NOS inhibitor N-G-nitro
-L-arginine (L-NA) in isolated rat basilar artel ies (BAs). 7-NINA had no s
ignificant effect on the resting tone of the vessels, while both L-NA and 1
H-[1,2,4]oxadiazolo[4,3-n]quinoxalin-1-one (ODQ), a selective inhibitor of
the soluble guanylyl cyclase, induced contraction. The relaxant effect of b
radykinin was attenuated in the presence of L-NA but was not changed by 7-N
INA. In contrast, 7-NINA markedly reduced the acetylcholine induced, endoth
elium-dependent relaxation. These results demonstrate that nNOS contributes
significantly to the relaxant effect of acetylcholine, indicating the func
tional importance of this isoenzyme in the cerebrovascular endothelium. (C)
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