EVALUATION OF THE ANTICONVULSANT ACTIVITY OF THE METHANOLEXTRACT OFTamarindusindica andFicusiteophylla LEAVES IN RODENTS
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Abstract
Epilepsy affects over 50 million people worldwide and imposes a treatment gap of 60–90% in low- and middle-income countries, including Nigeria, due to the cost and limited availability of conventional antiseizure medications. This study evaluated the
anticonvulsant-like potential of methanol leaf extracts of Ficus iteophylla (MEFI) and Tamarindus indica (METI) in mice, guided by their ethnomedicinal use in Nigerian traditional medicine for convulsions and neurological disorders.
Phytochemical screening confirmed alkaloids, glycosides, saponins, tannins, and reducing sugars in both extracts; terpenoids were present only in METI. Acute oral toxicity (Lorke’s method) yielded LD₅₀ > 5,000 mg/kg for MEFI and METI, with only
transient mild sedation at high doses, establishing a broad safety margin. Doses of 100, 200, and 400 mg/kg (p.o.) were selected for behavioral assays. Anticonvulsant evaluation employed the pentylenetetrazole (PTZ)-induced seizure
model (GABAergic modulation) and maximal electroshock seizure (MES) test (sodium channel blockade/seizure spread prevention). In the PTZ model, both extracts produced significant, dose-dependent protection, delaying seizure onset
and reducing severity (peak efficacy at 400 mg/kg for METI and 200 mg/kg for MEFI, comparable to diazepam 2 mg/kg and phenobarbitone 20 mg/kg). In the MES test, extracts displayed complex non-linear responses with partial protection at 200 and
400 mg/kg but inconsistent abolition of tonic hind-limb extension, failing to reach statistical significance for full sodium-channel blockade. Brain tissue analysis in nonseizing treated animals revealed enhanced antioxidant defense: elevated activities
of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR), with reduced malondialdehyde (MDA) levels. The robust anticonvulsant-like effects in the PTZ model, coupled with pronounced CNS antioxidant modulation and diverse neuroactive phytoconstituents, strongly support GABAergic enhancement and oxidative stress mitigation as primary mechanisms. Although MES outcomes were inconclusive, the findings validate ethnomedicinal claims for F. iteophylla and T. indica as safe, multi-mechanistic anticonvulsant candidates. Further studies with isolated fractions or alternative
solvents are warranted to optimize sodium-channel effects.
anticonvulsant-like potential of methanol leaf extracts of Ficus iteophylla (MEFI) and Tamarindus indica (METI) in mice, guided by their ethnomedicinal use in Nigerian traditional medicine for convulsions and neurological disorders.
Phytochemical screening confirmed alkaloids, glycosides, saponins, tannins, and reducing sugars in both extracts; terpenoids were present only in METI. Acute oral toxicity (Lorke’s method) yielded LD₅₀ > 5,000 mg/kg for MEFI and METI, with only
transient mild sedation at high doses, establishing a broad safety margin. Doses of 100, 200, and 400 mg/kg (p.o.) were selected for behavioral assays. Anticonvulsant evaluation employed the pentylenetetrazole (PTZ)-induced seizure
model (GABAergic modulation) and maximal electroshock seizure (MES) test (sodium channel blockade/seizure spread prevention). In the PTZ model, both extracts produced significant, dose-dependent protection, delaying seizure onset
and reducing severity (peak efficacy at 400 mg/kg for METI and 200 mg/kg for MEFI, comparable to diazepam 2 mg/kg and phenobarbitone 20 mg/kg). In the MES test, extracts displayed complex non-linear responses with partial protection at 200 and
400 mg/kg but inconsistent abolition of tonic hind-limb extension, failing to reach statistical significance for full sodium-channel blockade. Brain tissue analysis in nonseizing treated animals revealed enhanced antioxidant defense: elevated activities
of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR), with reduced malondialdehyde (MDA) levels. The robust anticonvulsant-like effects in the PTZ model, coupled with pronounced CNS antioxidant modulation and diverse neuroactive phytoconstituents, strongly support GABAergic enhancement and oxidative stress mitigation as primary mechanisms. Although MES outcomes were inconclusive, the findings validate ethnomedicinal claims for F. iteophylla and T. indica as safe, multi-mechanistic anticonvulsant candidates. Further studies with isolated fractions or alternative
solvents are warranted to optimize sodium-channel effects.
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