Previously, we demonstrated that endogenous circulating relaxin promot
es growth of the mammary nipples during the second half of pregnancy i
n the rat. The objective of this study was to determine whether relaxi
n acts directly on rat nipples to promote their growth. Initially, spe
cific relaxin-binding cells were identified to assure that relaxin bin
ds to the same cell types in the nipples of nonpregnant rats as those
we previously described in pregnant rats. To examine relaxin-induced g
rowth of the mammary nipples, 5 days after ovariectomy, 48 nonpregnant
rats were assigned (12 rats/group) to 1 of the following 4 treatment
groups: ovariectomized controls, estrogen treated, relaxin treated, an
d estrogen plus relaxin treated. Estrogen (0.05 mu g 17 beta-estradiol
) or estradiol vehicle (0.1 mi stripped corn oil) was administered sc
on the dorsal side of the neck daily for the entire 10-day treatment p
eriod. Porcine relaxin (12.5 mu g) or relaxin vehicle (0.05 mi 5% bees
wax in corn oil) was administered sc at the base of the left abdominal
nipple daily for the last 5 days of the 10-day treatment period. Afte
r hormone treatments, the lengths and wet weights of the left (relaxin
-treated) and right (untreated) abdominal nipples were measured. There
were three findings. First, the presence of specific relaxin binding
in the epithelial cells of the lactiferous duct, smooth muscle cells,
and skin of the nipples in nonpregnant rats was identical to the sites
of specific relaxin binding in the nipples of pregnant rats. Second,
relaxin-induced increases in nipple length and wet weight were mediate
d at least in part by the direct effects of relaxin in the nipple. Thi
rd, estrogen was not required for relaxin-induced increases in nipple
length and wet weight. We conclude that relaxin stimulates the growth
of rat mammary nipples at least in part through direct actions in the
nipples, and that estrogen is not required for these actions.