The aims of the present study were to characterize the expression and cellu
lar localization of isoforms of nitric oxide synthase (NOS) in the human co
rpus luteum (CL) and to determine the effects of nitric oxide (NO) on CL st
eroidogenesis, Immunoblotting analyses revealed that endothelial MOS (eNOS)
is the most abundant isoform in human CL with highest values during the la
te luteal phase. Immunoreactive eNOS was localized predominantely in the th
eca lutein layer, being particularly abundant in endothelial cells, but wit
h positive staining also in some steroidogenic cells. Immunoreactive induci
ble NOS (iNOS) was also detected, but to lesser degree, and did not display
apparent phase-specific changes. The effect of NO on CL steroid synthesis
was examined using human chorionic gonadotrophin (HCG)-stimulated dispersed
CL cells cultured in vitro, Progesterone production was significantly decr
eased (P < 0.05) by the MO donor spermine NONOate (10(-5) mol/l) in cells o
f the late, but not mid-, luteal phase. To investigate a potential link bet
ween NO and the local prostaglandins (PG), concentrations of PGF(2 alpha) a
nd PGE(2) were measured in culture medium. NO significantly increased (P <
0.05) concentrations of both PGF(2 alpha) and PGE(2) during the late luteal
phase, It is concluded that NO may be luteolytic in the human CL of menstr
uation.