Cargando…

Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures

Calcium ion participates in the regulation of neural transmission and the presynaptic release of neurotransmitters. It is also involved in epileptic events, cardiac arrhythmias and abnormal conduction of stimuli. The purpose of the present study was to evaluate the effects of nifedipine, a calcium c...

Descripción completa

Detalles Bibliográficos
Autores principales: Damasceno, D.D., Ferreira, A.J., Doretto, M.C., Almeida, A.P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Medicina Tropical 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854160/
https://www.ncbi.nlm.nih.gov/pubmed/22801414
http://dx.doi.org/10.1590/S0100-879X2012007500119
_version_ 1782294744802525184
author Damasceno, D.D.
Ferreira, A.J.
Doretto, M.C.
Almeida, A.P.
author_facet Damasceno, D.D.
Ferreira, A.J.
Doretto, M.C.
Almeida, A.P.
author_sort Damasceno, D.D.
collection PubMed
description Calcium ion participates in the regulation of neural transmission and the presynaptic release of neurotransmitters. It is also involved in epileptic events, cardiac arrhythmias and abnormal conduction of stimuli. The purpose of the present study was to evaluate the effects of nifedipine, a calcium channel blocker, on epileptic seizures and on reperfusion arrhythmias in rats prone to audiogenic epileptic seizures (Wistar audiogenic rats, WAR) and in normal Wistar rats (N = 6/group). The seizure severity index was applied after an intraperitoneal injection of 20 or 40 mg/kg nifedipine (N20 and N40 groups, respectively). The Langendorff technique was used to analyze cardiac function, as well as the incidence and severity of the reperfusion arrhythmias after ligature and release of the left coronary artery in rats treated or not with nifedipine. We found that nifedipine treatment decreased seizure severity (0.94 ± 0.02 for WAR; 0.70 ± 0.10 for WAR + N20; 0.47 ± 0.08 for WAR + N40) and increased the latent period (13 ± 2 s for WAR; 35 ± 10 s for WAR + N20; 48 ± 7 s for WAR + N40) for the development of seizures in WAR. Furthermore, the incidence and severity of the reperfusion arrhythmias were lower in WAR and normal Wistar rats injected with nifedipine. In WAR, these effects were mediated, at least in part, by a decrease in heart rate. Thus, our results indicate that nifedipine may be considered to be a potential adjuvant drug for epilepsy treatment, especially in those cases associated with cardiac rhythm abnormalities.
format Online
Article
Text
id pubmed-3854160
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Sociedade Brasileira de Medicina Tropical
record_format MEDLINE/PubMed
spelling pubmed-38541602013-12-16 Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures Damasceno, D.D. Ferreira, A.J. Doretto, M.C. Almeida, A.P. Braz J Med Biol Res Short Communication Calcium ion participates in the regulation of neural transmission and the presynaptic release of neurotransmitters. It is also involved in epileptic events, cardiac arrhythmias and abnormal conduction of stimuli. The purpose of the present study was to evaluate the effects of nifedipine, a calcium channel blocker, on epileptic seizures and on reperfusion arrhythmias in rats prone to audiogenic epileptic seizures (Wistar audiogenic rats, WAR) and in normal Wistar rats (N = 6/group). The seizure severity index was applied after an intraperitoneal injection of 20 or 40 mg/kg nifedipine (N20 and N40 groups, respectively). The Langendorff technique was used to analyze cardiac function, as well as the incidence and severity of the reperfusion arrhythmias after ligature and release of the left coronary artery in rats treated or not with nifedipine. We found that nifedipine treatment decreased seizure severity (0.94 ± 0.02 for WAR; 0.70 ± 0.10 for WAR + N20; 0.47 ± 0.08 for WAR + N40) and increased the latent period (13 ± 2 s for WAR; 35 ± 10 s for WAR + N20; 48 ± 7 s for WAR + N40) for the development of seizures in WAR. Furthermore, the incidence and severity of the reperfusion arrhythmias were lower in WAR and normal Wistar rats injected with nifedipine. In WAR, these effects were mediated, at least in part, by a decrease in heart rate. Thus, our results indicate that nifedipine may be considered to be a potential adjuvant drug for epilepsy treatment, especially in those cases associated with cardiac rhythm abnormalities. Sociedade Brasileira de Medicina Tropical 2012-07-20 /pmc/articles/PMC3854160/ /pubmed/22801414 http://dx.doi.org/10.1590/S0100-879X2012007500119 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Damasceno, D.D.
Ferreira, A.J.
Doretto, M.C.
Almeida, A.P.
Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures
title Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures
title_full Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures
title_fullStr Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures
title_full_unstemmed Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures
title_short Anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures
title_sort anticonvulsant and antiarrhythmic effects of nifedipine in rats prone to audiogenic seizures
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854160/
https://www.ncbi.nlm.nih.gov/pubmed/22801414
http://dx.doi.org/10.1590/S0100-879X2012007500119
work_keys_str_mv AT damascenodd anticonvulsantandantiarrhythmiceffectsofnifedipineinratspronetoaudiogenicseizures
AT ferreiraaj anticonvulsantandantiarrhythmiceffectsofnifedipineinratspronetoaudiogenicseizures
AT dorettomc anticonvulsantandantiarrhythmiceffectsofnifedipineinratspronetoaudiogenicseizures
AT almeidaap anticonvulsantandantiarrhythmiceffectsofnifedipineinratspronetoaudiogenicseizures