CORTICOTROPIN-RELEASING HORMONE (CRH) INHIBITS STEROID-BIOSYNTHESIS BY CULTURED HUMAN GRANULOSA-LUTEIN CELLS IN A CRH AND INTERLEUKIN-1 RECEPTOR-MEDIATED FASHION
L. Ghizzoni et al., CORTICOTROPIN-RELEASING HORMONE (CRH) INHIBITS STEROID-BIOSYNTHESIS BY CULTURED HUMAN GRANULOSA-LUTEIN CELLS IN A CRH AND INTERLEUKIN-1 RECEPTOR-MEDIATED FASHION, Endocrinology, 138(11), 1997, pp. 4806-4811
The presence of immunoreactive CRH was recently demonstrated in human
ovaries. CRH immunoreactivity was localized by immunohistochemistry in
the cytoplasm of thecal cells surrounding the ovarian follicles, in l
uteinized cells of the stroma, and in large granulosa derived luteiniz
ed cells of developing corpora lutea. Also, CRH and its receptors were
identified in Leydig cells of the testis where CRH was shown to inhib
it testosterone biosynthesis. To examine the role of CRH in the ovary,
we studied its effect on estradiol (E-2) and progesterone (P-4) relea
se by human granulosa cells obtained from women undergoing in vitro fe
rtilization for male factor infertility or uni-or bilateral tubal impa
tency. In all subjects, superovulation was induced by treatment ui th
gonadotropins. The effects of graded doses of ovine CRH (10(-11)-10(-6
) mol/liter) were evaluated in the conditioned medium obtained after 2
4 h incubation of the cells. All CRH concentrations employed except fo
r the lowest one (10(-11) mol/liter) caused a significant decrease of
media E-2 and P-4 levels. Maximal inhibition for both E-2 and P-4 prod
uction was obtained by 10(-6) mol/liter CRH concentration, which decre
ased hormone production by 39% and 34%, respectively. The alpha-helica
l CRH9-41 antagonist at 10(-6) and 10(-7) mol/liter blocked the suppre
ssive effect of 10(-9) mol liter CRH on both E-2 and P-4 secretion, wh
ile it had no effect when added to the culture media without CRH. Sinc
e interleukin (IL-1)-1 mediates certain actions of CRH on leukocytes,
we examined whether the CRH effect on ovarian steroidogenesis was IL-1
-mediated. Interleukin-1 receptor antagonist at 10(-7) and 10(-6) mol/
liter blocked the inhibitory effects of CRH on E-2 and P-4 secretion,
while it had no effect in the absence of CRH. In conclusion, CRH exert
s a CRH-and IL-1 receptor-mediated inhibitory effect on ovarian steroi
dogenesis and might be actively involved in the still enigmatic proces
ses of follicular atresia and luteolysis.