Anticonvulsant activity of Pseudospondias microcarpa (A. Rich) Engl. hydroethanolic leaf extract in mice: the role of excitatory/inhibitory neurotransmission and nitric oxide pathway

Publication date: Available online 17 May 2017
Source:Journal of Ethnopharmacology
Author(s): Donatus W. Adongo, Priscilla K. Mante, Kennedy K.E. Kukuia, Robert P. Biney, Eric Boakye-Gyasi, Charles K. Benneh, Elvis O. Ameyaw, Eric Woode
Ethnopharmacological relevancePseudospondias microcarpa (A. Rich) Engl. is a plant used for managing various diseases including central nervous system disorders.Aim of the studyThis study explored the anticonvulsant activity of P. microcarpa hydroethanolic leaf extract (PME) as well as possible mechanism(s) of action in animal models.MethodsEffects of PME was assessed in electroconvulsive (the maximal electroshock and 6-Hz seizures) and chemoconvulsive (pentylenetetrazole-, picrotoxin-, isoniazid-, 4-aminopyridine-, and strychnine-induced seizures) models of epilepsy. In addition, effect of the extract on the nitric oxide pathway and GABAA receptor complex was evaluated.ResultsThe extract (30, 100 and 300mgkg^-1, p.o.) significantly delayed the onset as well as decreased the duration and frequency of pentylenetetrazole-, picrotoxin- and strychnine-induced seizures. In addition, PME pre-treatment significantly improved survival in the 4-aminopyridine- and isoniazid-induced seizure tests. Furthermore, the extract protected against 6-Hz psychomotor seizures but had no effect in the maximal electroshock test. The anticonvulsant effect of PME (100mgkg^-1, p.o.) was also reversed by pre-treatment with flumazenil, L-arginine or sildenafil. However, L-NAME or methylene blue (MB) augmented its effect.ConclusionResults show that PME has anticonvulsant activity and may probably be affecting GABAergic, glycinergic, NMDA, K⁺ channels and nitric oxide-cGMP pathways to exert its effect.

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