Oxytocin is present in the mammalian testis where it increases contrac
tility of seminiferous tubules in vitro and has been implicated in spe
rm transport. The present study investigated whether oxytocin affects
the transport of spermatozoa from the testis in vivo. In rats, mature
spermatozoa are first seen in the testis 42 days postpartum and arrive
in the epididymis at about day 45. Male Wistar rats were given daily
subcutaneous injections of either oxytocin (0.5 mu g), the oxytocin an
tagonist des Gly-NH(2)d(CH2)(5)-[D-Tyr(2),Thr(4)]OVT (0.2 mu g) or sal
ine from day 40 postpartum. Groups of six animals were killed 2 h afte
r their last injection on days 43, 44, 45 and 46 postpartum. Testes we
re removed and fixed in Bouin's fluid for histological examination and
the number of spermatozoa in the epididymides was counted. Spermatozo
a were seen in the epididymis earlier in the oxytocin-treated rats (da
y 43) than in the control animals (day 44), and treatment with the ant
agonist delayed the appearance of spermatozoa in the-epididymis until
day 45. When the testes were examined, residual bodies, which were use
d as an indicator of spermiation, were seen only in one control animal
before day 44. Residual bodies were seen in the testes of all oxytoci
n-treated rats on day 43 but were not detected until day 45 in the oxy
tocin antagonist-treated rats. These data show that in rats oxytocin c
an affect the arrival of spermatozoa in the epididymis. Although this
may be due in part to effects on tubal transport or the secretion of t
ubular fluid, these findings suggest that the peptide may affect sperm
iation.