The effects of 17β-estradiol on ischemia-induced neuronal damage in the gerbil hippocampus

The effects of 17 beta-estradiol, a potent estrogen, on ischemia-induced neuronal damage, membrane depolarization and changes in intracellular Ca2+ concentration were studied in gerbil hippocampi. The histological outcome evaluated seven days after 3 min of transient forebrain ischemia in hippocampal CA1 pyramidal cells was improved by high doses of 17 beta-estradiol (30 mu g, i.c.v. and 4 mg/kg. i.p.), whereas low doses of 17 beta-estradiol (3 and 10 mu g, i.c.v.) showed no protective effect. Administration of 17 beta-estradiol did not affect the changes in the direct current potential shift in ischemia in the hippocampal CA1 area at any dosage. A hypoxia-induced intracellular Ca2+ increase was evaluated by in vitro microfluorometry in gerbil hippocampal slices. Pretreatment of 17 beta-estradiol (4 mg/kg, injected i.p. 1 h before decapitation) suppressed the increase in the intracellular concentration of Ca2+ due to the in vitro hypoxia, affecting both the onset of the increase and the extent. The in vitro hypoxia in the Ca2+ free condition induced an elevation of the intracellular concentration of Ca2+, although the increase was gradual. Pretreatment of 17 beta-estradiol (4 mg/kg, i.p.) also inhibited this elevation. These findings imply that high doses of 17 beta-estradiol protect the neurons from ischemia by inhibiting the release of Ca2+ from the intracellular Ca2+ stores, as well as by inhibiting the influx of Ca2+ from the extracellular space. (C) 1998 IBRO. Published by Elsevier Science Ltd.