A. Parra et al., ACUTE DOPAMINERGIC BLOCKADE AUGMENTS THE NALOXONE-INDUCED LH RISE IN ESTROGEN-TREATED POSTMENOPAUSAL WOMEN, Maturitas, 27(1), 1997, pp. 91-99
Objectives: To assess the effect of estrogen replacement on the simult
aneous blockade of the dopaminergic (DA) and opioidergic neural contro
l of hypothalamic-gonadotropic function in postmenopausal women. Metho
ds: Twenty healthy postmenopausal women, 48-55 years old were randomly
assigned to receive either a 4-h naloxone infusion at 2 mg/h (group 1
, n = 7) or a 10 mg i.v. bolus of metoclopramide (group 2, n = 7) or b
oth drugs: simultaneously (group 3, n = 6) before and after 3 weeks of
transdermal estradiol (100 mu g/day). Blood samples were obtained at
30-min intervals during 4 h and duplicate determinations of serum foll
icle-stimulating hormone (FSH), luteinizing hormone (LH), estradiol (E
-2) and prolactin (PRL) were performed in all samples. Results: In gro
up 1 only a mild but significant LH rise after but not before estrogen
replacement was seen. In group 2 PRL had a greater rise after than be
fore estrogen therapy, without other hormonal changes. In group 3 a gr
eater rise in PRL occurred after than before estrogen administration a
nd serum LH had a sustained rise throughout the test only after estrog
en replacement (greater than in group 1). No FSH changes were observed
. The after-estradiol PRL response was nearly similar in groups 2 and
3. Conclusions: Our results indicate that in the untreated postmenopau
sal women, the dopaminergic system has little and the opioidergic syst
em has no significant input in the control of gonadotropin or prolacti
n release. However, following estrogen replacement, opioids are involv
ed in the inhibition of LK release and stimulating PRL release, while
the dopaminergic system acts to inhibit PRL release and modulates LH r
elease or inhibition, depending on the levels of circulating estrogens
. (C) 1997 Elsevier Science Ireland Ltd.