By testing the effects of antecedent copulation on subsequent apomorph
ine-induced penile erection we sought to test an implicit assumption i
n the research on drug-induced ''spontaneous'' erection-namely, that t
his research provides information relevant to the regulation of erecti
on in copula. In experiment 1, male rats were observed after being inj
ected SC with 0, 15, 30, 60, or 120 mu g/kg apomorphine (APO); 60 mu g
/kg yielded the maximum probability of erection and yawning. In experi
ment 2, males were injected with 60 mu g/kg APO after no exposure to f
emales, after three intromissions, or after copulation to sexual satie
ty. There was no significant effect of three intromissions, but sexual
ly sated males displayed no erections, the first evidence that copulat
ion affects drug-induced erections. In experiment 3, males had one eja
culation, three intromissions, or no exposure to females immediately b
efore injection with APO (60 mu g/kg, SC) or ascorbic acid vehicle. AP
O induced both erection and yawning, but neither behavior was reliably
affected by copulation in APO-treated males. Among vehicle-treated ma
les, those having three intromissions or one ejaculation before the te
st had shorter erection latencies and more erections than males not ex
posed to females. Thus, a relatively small amount of copulation result
ed in a level of erectile response similar to that of APO-treated male
s. Optimal doses of APO may be no more effective in promoting erection
in male rats than are the natural neurochemical sequelae to copulatio
n.