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Department of Obstetrics and Gynecology and Center for Research in Reproductive Biology, Yale University, New Haven, Connecticut 06520
Address all correspondence and requests for reprints to: Tamas L. Horvath, Yale Medical School, Department of Obstetrics and Gynecology, 333 Cedar Street, FMB 339, New Haven Connecticut, 06520. E-mail: HorvathTA{at}MASPO1.MAS.YALE.EDU
Interactions between glutamate and gonadal steroids are involved in the
regulation of limbic and hypothalamic functions. We hypothesized that
hormonal signals affect excitatory neurotransmission by regulating the
expression of glutamate receptors (GluR) in limbic and hypothalamic
regions. To test this hypothesis, first, the coexpression of
dl-
-amino-3-hydroxy-5-methyl-4-isoxazone-propionate
(AMPA) GluR1, GluR2/3, and androgen receptors or estrogen receptors was
revealed in the same cells of septal, amygdaloid, and hypothalamic
areas by double immunocytochemistry. The highest incidence of
colocalization was detected in hypothalamic regions. To demonstrate a
regulatory role of testosterone or estradiol on AMPA receptor
expression, the hormonal milieu of male and female rats was manipulated
by gonadectomy and hormonal treatment. GluR1 and GluR2/3 expression was
assessed by Western blots. Statistical analysis demonstrated that
testosterone and estradiol have a stimulatory influence on the
expression of AMPA receptors in the hypothalamus. The regulatory effect
of estradiol on AMPA receptors was found to be site and gender
specific: after estradiol treatment, samples taken from the
hypothalamus contained increased levels of GluR1 and GluR2/3, whereas
in the septum, bed nucleus and amygdala, no changes could be detected.
Furthermore, the increase in hypothalamic GluR 2/3 levels was two times
higher in females, compared with males, whereas the changes in
hypothalamic GluR 1 levels showed no sex differences.
Our results support the hypothesis that the interaction between gonadal steroids and glutamate involves hormone regulation of GluR. This mechanism seems to be gender and site specific, suggesting that excitatory neurotransmission and related physiological mechanisms also may be distinctly different in males and females.
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