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Suramin inhibits beta-bungarotoxin-induced
activation of N-methyl-D-aspartate receptors and
cytotoxicity in primary neurons. / In conclusion, the novel
finding of this study was that a polypeptide beta-BuTX
exerted a potent cytotoxic effect through sequential events,
including activating NMDA receptors followed by increasing
[Ca2+]i, ROS production, and impaired mitochondrial energy
metabolism. Suramin, clinically used as a trypanocidal
agent, was an effective antagonist against beta-BuTX.