Posted by Chantel Martiromo. research contributed by PubMed
Isoflavonoids
are plant estrogens that are increasingly advocated as a
natural alternative to estrogen replacement therapy (ERT) and are
available as dietary supplements. As weak estrogen agonists/antagonists
with a range of other enzymatic activities, the isoflavonoids provide a
useful model for the actions of endocrine disruptors. According to the
study by the Emory University, treatment of rat dams with a 100-ppm
coumestrol diet from birth to
postnatal day (PND) 21 induced premature anovulation in female
offspring, and treatment from birth to PND 10 suppressed sexual behavior
in male offspring. One-week treatment of ovariectomized (OVX) female
rats with the same coumestrol diet increased ERbeta mRNA expression in
the PVN, an effect opposite to that of estradiol. Ten days of treatment
with a 200-ppm coumestrol diet increased LH secretion in OVX wild-type
mice, an effect opposite to the normal negative feedback effects of
estradiol. No effects were observed in ER(alpha) knockout
(ER(alpha)KO)-OVX females, indicating that coumestrol's action on LH was
mediated through ER(alpha). Similar activational effects were observed
for the isoflavone diet. The lordotic response to estrogen was
significantly reduced by 2 days of treatment of OVX adult females with
an isoflavone diet providing 13 ppm genistein and 33 ppm daidzein. One
week of treatment with the same isoflavone diet produced an effect
opposite to that of estradiol in the PVN, increasing ERbeta mRNA
expression above control levels. These investigations show that, in
spite of their preferential affinity for ERbeta, isoflavonoids act
through both ER(alpha) and ERbeta. Moreover, their neurobehavioral
actions were antiestrogenic, either antagonizing or producing an action
in opposition to that of estradiol. This work demonstrates that even
small, physiologically relevant exposure levels can alter
estrogen-dependent gene expression in the brain and complex behavior,
posted in PubMed.
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