Cargando…

Experimental re-evaluation of flunarizine as add-on antiepileptic therapy

BACKGROUND: Experimental studies have found several calcium channel blockers with anticonvulsant property. Flunarizine is one of the most potent calcium channel blockers, which has shown anticonvulsant effect against pentylenetetrazole (PTZ) and maximal electroshock (MES)-induced seizures. However,...

Descripción completa

Detalles Bibliográficos
Autores principales: Thakur, Anamika, Sahai, A. K., Thakur, J. S.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103921/
https://www.ncbi.nlm.nih.gov/pubmed/21687355
http://dx.doi.org/10.4103/0975-7406.80782
_version_ 1782204573295837184
author Thakur, Anamika
Sahai, A. K.
Thakur, J. S.
author_facet Thakur, Anamika
Sahai, A. K.
Thakur, J. S.
author_sort Thakur, Anamika
collection PubMed
description BACKGROUND: Experimental studies have found several calcium channel blockers with anticonvulsant property. Flunarizine is one of the most potent calcium channel blockers, which has shown anticonvulsant effect against pentylenetetrazole (PTZ) and maximal electroshock (MES)-induced seizures. However, further experimental and clinical trials have shown varied results. We conducted a PTZ model experimental study to re-evaluate the potential of flunarizine for add-on therapy in the management of refractory epilepsy. MATERIALS AND METHODS: Experiments were conducted in PTZ model involving Swiss strain mice. Doses producing seizures in 50% and 99% mice, i.e. CD(50) and CD(99) values of PTZ were obtained from the dose-response study. Animals received graded, single dose of sodium valproate (100–300 mg/kg), lamotrigine (3–12 mg/kg) and flunarizine (5–20 mg/kg), and then each group of mice was injected with CD(99) dose of PTZ (65mg/kg i.p.). Another group of mice received single ED(50) dose (dose producing seizure protection in 50% mice) of sodium valproate and flunarizine separately in left and right side of abdomen. Results were analysed by Kruskal–Wallis ANOVA on Ranks test. RESULTS: As compared to control, sodium valproate at 250 mg/kg and 300 mg/kg produced statistical significant seizure protection. At none of the pre-treatment dose levels of lamotrigine, the seizure score with PTZ differed significantly from that observed in the vehicle-treated group. Pre-treatment with flunarizine demonstrated dose-dependent decrease in the seizure score to PTZ administration. As compared to control group, flunarizine at 20 mg/kg produced statistical significant seizure protection. CONCLUSION: As combined use of sodium valproate and flunarizine has shown significant seizure protection in PTZ model, flunarizine has a potential for add-on therapy in refractory cases of partial seizures. It is therefore, we conclude that further experimental studies and multicenter clinical trials involving large sample size are needed to establish flunarizine as add-on therapy in refractory epilepsy.
format Text
id pubmed-3103921
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Medknow Publications Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-31039212011-06-16 Experimental re-evaluation of flunarizine as add-on antiepileptic therapy Thakur, Anamika Sahai, A. K. Thakur, J. S. J Pharm Bioallied Sci Original Article BACKGROUND: Experimental studies have found several calcium channel blockers with anticonvulsant property. Flunarizine is one of the most potent calcium channel blockers, which has shown anticonvulsant effect against pentylenetetrazole (PTZ) and maximal electroshock (MES)-induced seizures. However, further experimental and clinical trials have shown varied results. We conducted a PTZ model experimental study to re-evaluate the potential of flunarizine for add-on therapy in the management of refractory epilepsy. MATERIALS AND METHODS: Experiments were conducted in PTZ model involving Swiss strain mice. Doses producing seizures in 50% and 99% mice, i.e. CD(50) and CD(99) values of PTZ were obtained from the dose-response study. Animals received graded, single dose of sodium valproate (100–300 mg/kg), lamotrigine (3–12 mg/kg) and flunarizine (5–20 mg/kg), and then each group of mice was injected with CD(99) dose of PTZ (65mg/kg i.p.). Another group of mice received single ED(50) dose (dose producing seizure protection in 50% mice) of sodium valproate and flunarizine separately in left and right side of abdomen. Results were analysed by Kruskal–Wallis ANOVA on Ranks test. RESULTS: As compared to control, sodium valproate at 250 mg/kg and 300 mg/kg produced statistical significant seizure protection. At none of the pre-treatment dose levels of lamotrigine, the seizure score with PTZ differed significantly from that observed in the vehicle-treated group. Pre-treatment with flunarizine demonstrated dose-dependent decrease in the seizure score to PTZ administration. As compared to control group, flunarizine at 20 mg/kg produced statistical significant seizure protection. CONCLUSION: As combined use of sodium valproate and flunarizine has shown significant seizure protection in PTZ model, flunarizine has a potential for add-on therapy in refractory cases of partial seizures. It is therefore, we conclude that further experimental studies and multicenter clinical trials involving large sample size are needed to establish flunarizine as add-on therapy in refractory epilepsy. Medknow Publications Pvt Ltd 2011 /pmc/articles/PMC3103921/ /pubmed/21687355 http://dx.doi.org/10.4103/0975-7406.80782 Text en Copyright: © Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Thakur, Anamika
Sahai, A. K.
Thakur, J. S.
Experimental re-evaluation of flunarizine as add-on antiepileptic therapy
title Experimental re-evaluation of flunarizine as add-on antiepileptic therapy
title_full Experimental re-evaluation of flunarizine as add-on antiepileptic therapy
title_fullStr Experimental re-evaluation of flunarizine as add-on antiepileptic therapy
title_full_unstemmed Experimental re-evaluation of flunarizine as add-on antiepileptic therapy
title_short Experimental re-evaluation of flunarizine as add-on antiepileptic therapy
title_sort experimental re-evaluation of flunarizine as add-on antiepileptic therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103921/
https://www.ncbi.nlm.nih.gov/pubmed/21687355
http://dx.doi.org/10.4103/0975-7406.80782
work_keys_str_mv AT thakuranamika experimentalreevaluationofflunarizineasaddonantiepileptictherapy
AT sahaiak experimentalreevaluationofflunarizineasaddonantiepileptictherapy
AT thakurjs experimentalreevaluationofflunarizineasaddonantiepileptictherapy