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Anticonvulsant properties of an aqueous extract of Dysphania ambrosioides (L.) Mosyakin and Clemants (Chenopodiaceae) in mice pilocarpine model of temporal lobe epilepsy

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  • Anticonvulsant Properties of An Aqueous Extract of Dysphania Ambrosioides (L.) Mosyakin and Clemants (Chenopodiaceae) In Mice Pilocarpine Model of Temporal Lobe Epilepsy
  • Anticonvulsant properties of an aqueous extract of Dysphania ambrosioides (L.) Mosyakin and Clemants (Chenopodiaceae) in mice pilocarpine model of temporal lobe epilepsy

Bigued 1, *, Joseph Ngaibi 2, Antoine Kavaye Kandeda 3, Yvette Nguezeye 4, 5, Lamido Gaoudji 5, Tchang Alkali Wangbara 1, Germain Sotoing Taiwe 6 and Elisabeth Ngo Bum 1, 5

1 Department of Biological Sciences, Faculty of Science, University of Maroua, P.O. Box 814, Maroua, Cameroon.
2 Department of Animal Biology, Faculty of Science, University of Dschang, Cameroon, P.O. Box 67, Dschang, Cameroon.
3 Department of Animal Biology and Physiology, University of Yaounde I, P.O. Box 812, Yaounde, Cameroon.
4 Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies, P.O. Box 13033, Yaounde, Cameroon.
5 Department of Biological Sciences, Faculty of Science, University of Ngaoundere, P.O. Box 454, Ngaoundéré, Cameroon.
6 Department of Animal Biology and Conservation, Faculty of Science, University of Buea, Cameroon, P.O. Box 63, Buea, Cameroon.
 
Research Article
GSC Advanced Research and Reviews, 2024, 19(03), 164–175.
Article DOI: 10.30574/gscarr.2024.19.3.0203
DOI url: https://doi.org/10.30574/gscarr.2024.19.3.0203
Received on 28 April 2024; revised on 06 June 2024; accepted on 08 June 2024
 
Ethnopharmacological relevance: Dysphania ambrosioides (L.) Mosyakin and Clemants (Chenopodiaceae) is used in traditional Cameroonian medicine to treat epilepsy and anxiety.
Aims of the study: This study aimed to investigate the anticonvulsant effects of Dysphania ambrosioides aqueous extract in mice pilocarpine model of temporal lobe epilepsy.
Materials and Methods: The mice were treatments with distilled water for the normal and negative control, sodium valproate (300 mg/kg) for the positive control, and different doses of an aqueous extract of Dysphania ambrosioides (37, 92.5, 185, 370 mg/kg, p.o) for the test groups. Methyl-scopolamine (1 mg/kg) were injected forty minute later. One hour after the first treatment (first day), epilepsy was induced by intraperitoneal injection of 360 mg/kg pilocarpine. On the seventh day, antioxidant activities and the involvement of GABAergic transmission were determined by measuring the levels of malondialdehyde (MDA), reduced glutathione (GSH), superoxide dismutase (SOD), catalase (CAT), γ-Aminobutyric acid (GABA) and GABA-transaminase (GABA-T), respectively in the hippocampus of sacrificed epileptic mice.
Results: Dysphania ambrosioides (370 mg/kg) strongly protected mice against epileptogenesis by increasing the latency time to status epilepticus (p˂0.001) and decreasing the number of tonic clonic convulsions (p˂0.001). The extract significantly increased the levels of GSH (p˂0.001), CAT (p˂0.001), SOD (p˂0.001) and GABA (p˂0.001), and decreased the levels of MDA (p˂0.001), NO (p˂0.001) and GABA-T (p˂0.001).
Conclusion: The results suggest that the anticonvulsant activities of Dysphania ambrosioides extract are accompanied by its antioxidant effects, and may be mediated at least in part by the GABA neurotransmission.
 
Anticonvulsant; Temporal Lobe Epilepsy; Γ-Aminobutyric Acid; Oxidative Stress; Dysphania Ambrosioides.
 
https://gscarr.gsconlinepress.com/sites/default/files/fulltext_pdf/GSCARR-2024-…

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Bigued, Joseph Ngaibi, Antoine Kavaye Kandeda, Yvette Nguezeye, Lamido Gaoudji, Tchang Alkali Wangbara, Germain Sotoing Taiwe and Elisabeth Ngo Bum. Anticonvulsant properties of an aqueous extract of Dysphania ambrosioides (L.) Mosyakin and Clemants (Chenopodiaceae) in mice pilocarpine model of temporal lobe epilepsy. GSC Advanced Research and Reviews, 2024, 19(3), 164-175. Article DOI: https://doi.org/10.30574/gscarr.2024.19.3.0203

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