Nitric oxide (NO) may mediate penile erection by inhibiting smooth mus
cle of the corpora cavernosa, thereby allowing vasodilation of the cor
pora. In order to test the role of NO in the sexual function of intact
male rats, either the precursor of NO (L-arginine, L-Arg) or an inhib
itor of its synthesis ((N)G-nitro-L-arginine methyl ester, NAME) was a
dministered systemically before tests of copulation, ex copula genital
reflexes, or sexual motivation/motor activity. NAME impaired copulati
on in a dose dependent manner. It also decreased the number of ex copu
la erections, but it increased the number of ex copula seminal emissio
ns and decreased the latency to the first seminal emission. L-Arg marg
inally increased the number of penile reflexes, but had no other effec
ts. NAME had no effect on sexual motivation or motor activity. The res
ults indicate that nitric oxide promotes erection in intact male rats,
probably by mediating filling of the corpora cavernosa. The data also
suggest that NO inhibits seminal emission, probably by decreasing sym
pathetic nervous system activity; this may help prevent premature ejac
ulation.