Abstract
In the present study, we show that the large conductance calcium-activated potassium channel (BKCa channel) inhibitor paxilline protects neuronal cells against glutamate-induced cell death. In our studies, we used HT22 mouse hippocampal cells as an experimental model and observed that the effect of paxilline was dose-dependent. We also found that other inhibitors of BKCa channels, iberiotoxin and charybdotoxin, were not cytoprotective. Paxillinol, which is a structural analog of paxilline but does not inhibit BKCa channel, also protected HT22 cells against glutamate-induced toxicity. These data suggest that the observed cytoprotection was not related to BKCa channel inhibition by paxilline. In addition, paxilline neither restored glutathione levels nor reduced the amount of reactive oxygen species upon glutamate treatment.Our results suggest that paxilline protects neuronal HT22 cells against glutamate-induced cell death independently of BKCa channel activity and oxidative stress induced by glutamate treatment.
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