ESTROGEN-RECEPTOR IMMUNOSTAINING IN THE PREOPTIC AREA AND MEDIAL BASAL HYPOTHALAMUS OF ESTRADIOL BENZOATE-TREATED AND PRAZOSIN-TREATED FEMALE GUINEA-PIGS
Kf. Malik et al., ESTROGEN-RECEPTOR IMMUNOSTAINING IN THE PREOPTIC AREA AND MEDIAL BASAL HYPOTHALAMUS OF ESTRADIOL BENZOATE-TREATED AND PRAZOSIN-TREATED FEMALE GUINEA-PIGS, Journal of neuroendocrinology, 5(3), 1993, pp. 297-306
Evidence has accumulated showing that the alpha1-adrenergic antagonist
prazosin decreases nuclear estrogen binding in the hypothalamus of th
e guinea-pig. In this study we asked if prazosin treatment alters estr
ogen receptor (ER) protein content as reflected by changes in ER-immun
oreactivity. The monoclonal rat antibody H222 directed against ER was
used to detect ER-immunoreactive (ER-ir) cells in eight specific preop
tic and hypothalamic brain regions of ovariectomized Hartley strain gu
inea-pigs treated with estradiol benzoate and 1.0 mg/kg prazosin or ve
hicle. Immunocytochemical parameters which provided optimum conditions
for detection of even modest changes in ER-immunoreactivity were firs
t established. Then, using these optimum conditions, we compared 1) th
e mean number of ER-ir profiles, 2) the mean density of ER-ir staining
, and 3) the distribution of ER-ir staining density readings, between
conditions within each of the eight brain regions. No differences in a
ny of these measures were found between prazosin- and vehicle-treated
females. We also compared the percentage of ER-ir nuclear profiles acr
oss the eight cell groups investigated in estradiol benzoate- and vehi
cle-treated females. The medial preoptic area had by far the highest p
ercentage (48%) of ER-ir profiles (P < 0.05) compared to all seven oth
er brain regions (23% to 32% ER-ir cells). Our data, showing that ER-i
mmunoreactivity is not reduced (6 h) after prazosin treatment, suggest
s that mechanisms other than alterations in ER protein should be consi
dered when interpreting the effects of prazosin on the retention of es
tradiol by nuclear or cytosolic extracts of hypothalamic lysates.