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and ß to Protect Hippocampal Neurons against Global Ischemia-Induced Cell Death
Department of Obstetrics, Gynecology and Women’s Health (N.R.M.), Division of Reproductive Endocrinology and Infertility; Department of Neuroscience (T.J., R.S.Z., A.M.E.); and Department of Epidemiology and Population Health (H.W.C.), Albert Einstein College of Medicine, Bronx, New York 10461
Address all correspondence and requests for reprints to: Anne M. Etgen, Ph.D., Albert Einstein College of Medicine, Department of Neuroscience, 1300 Morris Park Avenue, Forchheimer 113, Bronx, New York 10461. E-mail: etgen{at}aecom.yu.edu.
Estradiol at physiological concentrations intervenes in apoptotic death cascades and ameliorates neuronal death in experimental models of focal and global ischemia. The cellular targets that mediate estradiol protection of hippocampal neurons in global ischemia are, however, unclear. The present study examined the hypothesis that estradiol protects hippocampal neurons in ovariectomized rats via estrogen receptor (ER)
and/or ß. Estradiol (14 d pretreatment) afforded robust protection of CA1 neurons against global ischemia-induced death. The broad-spectrum ER antagonist ICI 182,780 (intracerebroventricularly, 0 and 12 h after ischemia) abolished estrogen protection, consistent with a role for ERs. To evaluate the potential roles of ER vs. ERß in estrogen protection, we administered subtype-selective agonists for 14 d before and 7 d after ischemia. The ER-selective agonist propyl pyrazole triol (PPT, 10 mg/kg) and ERß-selective agonist WAY 200070–3 (1 mg/kg) produced nearly complete protection of CA1 neurons in approximately 50% of the animals. PPT, but not WAY 200070–3, at doses used for protection, elicited lordosis, induced negative feedback inhibition of LH release, and reduced weight gain. These findings establish the efficacy of the PPT dose in neuroendocrine assays and specificity of WAY 200070–3 for ERß. We also examined the ability of estradiol and neuronal injury to regulate ER and ERß expression. Both estradiol and global ischemia markedly increased ER, but not ERß, protein in CA1. These data indicate that estradiol can act via ER and ERß to protect CA1 neurons from global ischemia-induced death and that both estradiol and global ischemia modulate ER expression in hippocampal CA1.
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