Keoxifene shows pure antiestrogenic activity in pituitary gonadotrophs

Abstract

Estrogens increase both basal and LHRH-induced LH release in rat anterior pituitary cells in culture. Following 48 h of preincubation with 1 nM 17β-estradiol, the maximal LH response to LHRH is increased 1.5-fold while the ED 50 value of LHRH action is decreased 2.5-fold from 500 to 200 pM. The maximal 3-fold stimulation of 0.3 nM LHRH-induced LH release by 17β-estradiol is exerted at a K D value of 14.4 pM. Keoxifene (300 nM) completely blocks the potent stimulatory effect of 17β-estradiol up to 1 nM, the highest concentration of the estrogen used. As shown by the complete reversal of the stimulatory effect of 0.1 and 1.0 nM 17β-estradiol by keoxifene at IC 50 values of 7.7 and 34 nM respectively, the antiestrogen interacts competitively with 17β-estradiol at the estrogen binding site. When present alone, keoxifene shows no estrogenic activity. The present data show that keoxifene acts as a pure antiestrogen on the control of LHRH-induced LH release in rat pituitary gonadotrophs.