Abstract
We investigated the anticonvulsant effect of acute Fuzi total alkaloid (FTA) in seizure induced by the GABAA-receptor antagonist pentylenetetrazole (PTZ). FTA significantly increased the seizure latency and decreased the mortality in PTZ-treated mice. Administration of PTZ increased c-Fos expression in the hippocampus, medial prefrontal cortex, and piriform cortex; and this PTZ-induced effect was inhibited by FTA in a dose-dependent manner. Furthermore, the effects of FTA on PTZ-induced seizure and c-Fos expression were reversed by the GABAA/benzodiazepine receptor-selective antagonist flumazenil. These findings suggest that the anticonvulsant effects of FTA may be related to modulation of GABA A-benzodiazepine receptor complex. © The Japanese Pharmacological Society.
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CITATION STYLE
Li, B., Tang, F., Wang, L., Liu, L., Zhao, J., Zhou, Y., … Cui, R. (2013). Anticonvulsant effects of Fuzi total alkaloid on pentylenetetrazole-induced seizure in mice. Journal of Pharmacological Sciences, 123(2), 195–198. https://doi.org/10.1254/jphs.13057SC
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