Estrogens have numerous reproductive and nonreproductive functions in brain
. The actions of estrogens are mediated by estrogen receptors (ERs), and es
trogens are believed to down-regulate their own receptors in many tissues.
Assuming this to be true, if estrogens are removed there should be an upreg
ulation of ERs. We have developed a mouse model in which estrogen synthesis
is completely eliminated by homologous recombination to delete the gene en
coding aromatase cytochrome P450 (P450(arom)). The P350(arom), enzyme catal
yzes the synthesis of estrogens from androgens in the brain. The localizati
on and density of ERs was studied in the brains of aromatase knockout (ArKO
) and wild type male mice by using immunohistochemistry with a peptide anti
body to ER alpha (ER-21) and computer imaging. In the wild-type animals a h
igh density of ER alpha. was found in a small number of hypothalamic cells;
in the medial preoptic area, periventricular, arcuate, and ventromedial nu
clei. A low and medium density of ER I was observed in cells of the lateral
preoptic area, supraoptic, bed nucleus of the stria terminalis, and in cen
tral, medial and anterior cortical amygdaloid nuclei. The number of cells c
ontaining ER alpha-immunoreactivity was significantly increased (244%) in t
he medial preoptic area of the ArKO mice. In neither wild type nor ArKO ani
mals was immunoreactivity observed in the cerebral cortex or striatum. Ther
e was intense ER-immunostaining in the nucleus of neurons in both wild type
and ArKO mice. These data indicate that in the absence of estrogens there
is as much as a 2-fold increase in the number of cells with ER alpha-immuno
reactivity in certain hypothalamic and limbic regions. Thus, estrogens can
down-regulate ER alpha in brain. (C) 2000 Elsevier Science Ireland Ltd. All
rights reserved.