Asparagus africanus Lam. (Asparagaceae) is a widely used plant in traditional medicine as an anti-inflammatory, antioxidant, for the treatment of nervous disorders and epilepsy. The objective of this work was to study the anticonvulsant effects of A. africanus root decoction in white mice (Mus musculus Swiss) induced by pilocarpine. The experimental induction of "status epilepticus" and the evaluation of the anticonvulsant effects of A. africanus root decoction on pilocarpine-induced clonic and tonic convulsions were carried out. Seizure severity, latency, duration and number of clonics and tonics convulsions were evaluated. Concentrations of GABA, GABA-T, TNF-α and stress markers in the brains of mice were also estimated. A. africanus decreased the duration and number of clonic and tonic convulsions which increased the latency time of onset of clonic and tonic convulsions significantly and in a dose-dependent manner. GABA increased significantly in the brains of animals treated with A. africanus and a significant decrease of GABA-T and TNF-α. A. africanus also showed antioxidant effects. These results show that A. africanus has anticonvulsant effects. A. africanus would thus contain beneficial antiradical constituents in the treatment of epilepsy. These constituents would thus oppose free radicals. These results would justify the use of this plant in traditional medicine in the treatment of epilepsy.
Asparagus africanus Lam. (Asparagaceae) is a plant widely used in traditional medicine as an anti-inflammatory, for the treatment of nervous disorders and insomnia. The aim of this work was to study the sedative and hypnotic effects of the roots of A. africanus decoction on white mice (Mus musculus Swiss). Sleep potentiation tests induced by diazepam and sodium pentobarbital were used. The sleep latency period onset and the sleep duration were recorded. The concentrations of GABA a[nd GABA-T in the brains of mice were also estimated. A. africanus significantly decreased the sleep latency period onset and increased the sleep duration induced by diazepam and sodium pentobarbital. Bicuculline, a competitive photosensitive antagonist of the GABAA receptor complex, did not prevent this potentiation. The effect of A. africanus on the sleep time was not blocked by flumazenil, a specific antagonist to the benzodiazepine site in the GABAA receptor complex. GABA increased and GABA-T decreased in the animals brain A. africanus treated significantly. Therefore the sedative properties of A. africanus might be possibly mediated by the activation of GABAergic neurotransmission on inhibitory receptors and by the decrease in the recapture of GABA by inhibiting GABA-T. These properties justified its use against insomnia in traditional medicine.
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