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- and ß-Dependent Gene Expression in the Brain1
Center for Behavioral Neuroscience (H.B.P., P.L.W., L.J.Y.) and Departments of Anthropology (P.L.W.) and Psychiatry and Behavioral Sciences (L.J.Y.), Emory University, Atlanta, Georgia 30329
Address all correspondence and requests for reprints to: Dr. Heather B. Patisaul, Center for Behavioral Neuroscience, Emory University, 954 Gatewood Road NE, Atlanta, Georgia 30329.
Epidemiological evidence suggests that isoflavone phytoestrogens may
reduce the risk of cancer, osteoporosis, and heart disease, effects at
least partially mediated by estrogen receptors
and ß (ER
and
ERß). Because isoflavone dietary supplements are becoming
increasingly popular and are frequently advertised as natural
alternatives to estrogen replacement therapy, we have examined the
effects of one of these supplements on estrogen-dependent behavior and
ER
- and ERß-dependent gene expression in the brain. In the adult
female rat brain, 17ß-estradiol treatment decreased ERß messenger
RNA signal in the paraventricular nucleus by 41%, but supplement
treatment resulted in a 27% increase. The regulation of ERß in the
paraventricular nucleus is probably via an ERß-dependent mechanism.
Similarly, in the ventromedial nucleus of the hypothalamus, supplement
treatment diminished the estrogen-dependent up-regulation of oxytocin
receptor by 10.5%. The regulation of oxytocin receptor expression in
the ventromedial nucleus of the hypothalamus is via an ER
-dependent
mechanism. Supplement treatment also resulted in a significant decrease
in receptive behavior in estrogen- and progesterone-primed females. The
observed disruption of sexual receptivity by the isoflavone supplement
is probably due to antiestrogenic effects observed in the brain. These
results suggest that isoflavone phytoestrogens are antiestrogenic on
both ER
- and ERß-dependent gene expression in the brain and
estrogen-dependent behavior.
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