Oestrogens protect neurons against excitatory amino acid-induced toxicity;
however data on their interaction with particular subtype of glutamate rece
ptors are sparse. Therefore in the present study we investigated oestrogen
effects on kainate neurotoxicity in primary cortical neurons. The data show
ed that both oestradiol-17 beta and oestrone (100 nM and 200 nM) reduced ka
inate toxicity by ca. 40%. Since tamoxifen only partly inhibited the above
effects, we suggest that both genomic and non-genomic mechanisms are involv
ed in the anti-kainate action of oestrogens.