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Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats
BACKGROUND: Mefloquine can cross the blood–brain barrier and block the gap junction intercellular communication in the brain. Enhanced electrical coupling mediated by gap junctions is an underlying mechanism involved in the generation and maintenance of seizures. For this reason, the aim of this stu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411716/ https://www.ncbi.nlm.nih.gov/pubmed/25886955 http://dx.doi.org/10.1186/s12868-015-0145-7 |
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author | Franco-Pérez, Javier Ballesteros-Zebadúa, Paola Manjarrez-Marmolejo, Joaquín |
author_facet | Franco-Pérez, Javier Ballesteros-Zebadúa, Paola Manjarrez-Marmolejo, Joaquín |
author_sort | Franco-Pérez, Javier |
collection | PubMed |
description | BACKGROUND: Mefloquine can cross the blood–brain barrier and block the gap junction intercellular communication in the brain. Enhanced electrical coupling mediated by gap junctions is an underlying mechanism involved in the generation and maintenance of seizures. For this reason, the aim of this study was to analyze the effects of the systemic administration of mefloquine on tonic-clonic seizures induced by two acute models such as pentylenetetrazole and maximal electroshock. RESULTS: All the control rats presented generalized tonic-clonic seizures after the administration of pentylenetetrazole. However, the incidence of seizures induced by pentylenetetrazole significantly decreased in the groups administered systematically with 40 and 80 mg/kg of mefloquine. In the control group, none of the rats survived after the generalized tonic-clonic seizures induced by pentylenetetrazole, but survival was improved by mefloquine. Besides, mefloquine significantly modified the total spectral power as well as the duration, amplitude and frequency of the epileptiform activity induced by pentylenetetrazole. For the maximal electroshock model, mefloquine did not change the occurrence of tonic hindlimb extension. However, this gap junction blocker significantly decreased the duration of the tonic hindlimb extension induced by the acute electroshock. CONCLUSIONS: These data suggest that mefloquine at low doses might be eliciting some anticonvulsant effects when is systemically administered to rats. |
format | Online Article Text |
id | pubmed-4411716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44117162015-04-29 Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats Franco-Pérez, Javier Ballesteros-Zebadúa, Paola Manjarrez-Marmolejo, Joaquín BMC Neurosci Research Article BACKGROUND: Mefloquine can cross the blood–brain barrier and block the gap junction intercellular communication in the brain. Enhanced electrical coupling mediated by gap junctions is an underlying mechanism involved in the generation and maintenance of seizures. For this reason, the aim of this study was to analyze the effects of the systemic administration of mefloquine on tonic-clonic seizures induced by two acute models such as pentylenetetrazole and maximal electroshock. RESULTS: All the control rats presented generalized tonic-clonic seizures after the administration of pentylenetetrazole. However, the incidence of seizures induced by pentylenetetrazole significantly decreased in the groups administered systematically with 40 and 80 mg/kg of mefloquine. In the control group, none of the rats survived after the generalized tonic-clonic seizures induced by pentylenetetrazole, but survival was improved by mefloquine. Besides, mefloquine significantly modified the total spectral power as well as the duration, amplitude and frequency of the epileptiform activity induced by pentylenetetrazole. For the maximal electroshock model, mefloquine did not change the occurrence of tonic hindlimb extension. However, this gap junction blocker significantly decreased the duration of the tonic hindlimb extension induced by the acute electroshock. CONCLUSIONS: These data suggest that mefloquine at low doses might be eliciting some anticonvulsant effects when is systemically administered to rats. BioMed Central 2015-03-01 /pmc/articles/PMC4411716/ /pubmed/25886955 http://dx.doi.org/10.1186/s12868-015-0145-7 Text en © Franco-Pérez et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Franco-Pérez, Javier Ballesteros-Zebadúa, Paola Manjarrez-Marmolejo, Joaquín Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats |
title | Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats |
title_full | Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats |
title_fullStr | Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats |
title_full_unstemmed | Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats |
title_short | Anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats |
title_sort | anticonvulsant effects of mefloquine on generalized tonic-clonic seizures induced by two acute models in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411716/ https://www.ncbi.nlm.nih.gov/pubmed/25886955 http://dx.doi.org/10.1186/s12868-015-0145-7 |
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