Dopamine depletion in wistar rats with epilepsy

Autor: E. M. Trindade-Filho, J. Dal Pai, D. N. de Castro, A. T. M. da Silva, A. F. Costa, J. S. S. Vieira, S. D. B. dos Santos, V. B. Félix, S. A. B. F. Leão, L. I. Zambrano, A. J. M. Saldanha-Filho, E. G. A. Carvalho, J. B. N. Cavalcante, G. B. Quintella, A. T. S. Lino, M. V. Costa, J. A. Lima, M. M. A. Tavares, M. R. de Melo, K. C. Mousinho, C. L. C. L. De Biase, M. L. Leite, P. J. M. S. Costa, E. L. Becker, I. M. F. B. Moura, J. C. da Silva
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Brazilian Journal of Biology, Vol 84 (2022)
Druh dokumentu: article
ISSN: 1678-4375
1519-6984
DOI: 10.1590/1519-6984.248411
Popis: Abstract The dopamine content in cerebral structures has been related to neuronal excitability and several approaches have been used to study this phenomenon during seizure vulnerability period. In the present work, we describe the effects of dopamine depletion after the administration of 6-hidroxidopamine (6-OHDA) into the substantia nigra pars compacta of male rats submitted to the pilocarpine model of epilepsy. Susceptibility to pilocarpine-induced status epilepticus (SE), as well as spontaneous and recurrent seizures (SRSs) frequency during the chronic period of the model were determined. Since the hippocampus is one of main structures in the development of this experimental model of epilepsy, the dopamine levels in this region were also determined after drug administration. In the first experiment, 62% (15/24) of 6-OHDA pre-treated rats and 45% (11/24) of those receiving ascorbic acid as control solution progressed to motor limbic seizures evolving to SE, after the administration of pilocarpine. Severeness of seizures during the model´s the acute period, was significantly higher in epileptic experimental rats (56.52%), than in controls (4.16%). In the second experiment, the frequency of seizures in the model’s chronic phase did not significantly change between groups. Our data show that dopamine may play an important role on seizure severity in the pilo’s model acute period, which seems to be due to dopamine inhibitory action on motor expression of seizure.
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