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2000
Volume 20, Issue 2
  • ISSN: 1871-5249
  • E-ISSN: 1875-6166

Abstract

Objective: To determine the potential effect of Pyrenancantha staudtii extract on experimentally induced seizures in mice and to evaluate the role of benzodiazepines, naloxone, and serotonin within these pathways. Methods: Animal behaviours were evaluated using open field, hexobarbitone-induced sleep model, and anticonvulsant activity using picrotoxin-, or strychnine-, or isoniazid-induced convulsions. Attempt to understand the mode of action of the anticonvulsant activity of the plant, three notable antagonists (flumazenil, 3 mg/kg; naloxone 5 mg/kg, i.p., and cyproheptadine, 4 mg/kg, i.p) were used. Results: The results revealed a significant (p < 0.05) reduction in the frequency of rearing and grooming episodes compared with the control. The extract of potentiates the sleeping time of hexobarbitone-induced hypnosis in a dose-related manner. stem bark extracts significantly (p<0.05) prolonged the onset of a seizure and attenuated the duration of seizure in a dose-dependent manner in picrotoxin- and or isoniazid-induced seizures. While, stem bark extract at all doses (100, 200, and 400 mg kg-1) though significantly prolonged the onset of action, but did not confer any significant changes on the duration, as well as mortality in this strychnine-induced seizure model. However, the anticonvulsant activity of the methanolic extract of was significantly reversed following intraperitoneal pre-treatment with flumazenil (GABA receptor antagonist) and naloxone (opioid receptor antagonist) but not cyproheptadine (5-HT receptor antagonist) in picrotoxin-induced convulsion. Conclusion: The data obtained suggest that methanol extract of possessed significant anticonvulsant effect, thereby confirming the traditional uses of in the treatment of epilepsy; mechanisms of which could involve the interaction with GABAergic and or opioidergic system.

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/content/journals/cnsamc/10.2174/1871524920666200211113633
2020-08-01
2025-10-15
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  • Article Type:
    Research Article
Keyword(s): cyproheptadine; hexobarbitone; isoniazid; picrotoxin; Pyrenancantha staudtii; strychnine
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