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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Effects of A1 receptor agonist/antagonist on spontaneous seizures in pilocarpine-induced epileptic rats

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Autor(es):
Amorim, Beatriz Oliveira ; Hamani, Clement ; Ferreira, Elenn ; Miranda, Maisa Ferreira ; Fernandes, Maria Jose S. ; Rodrigues, Antonio M. ; de Almeida, Antonio-Carlos G. ; Covolan, Luciene
Número total de Autores: 8
Tipo de documento: Artigo Científico
Fonte: Epilepsy & Behavior; v. 61, p. 168-173, AUG 2016.
Citações Web of Science: 2
Resumo

Adenosine is an endogenous anticonvulsant that activates pre- and postsynaptic adenosine A(1) receptors. A(1) receptor agonists increase the latency for the development of seizures and status epilepticus following pilocarpine administration. Although hippocampal adenosine is increased in the chronic phase of the pilocarpine model, it is not known whether the modulation of A(1) receptors may influence the frequency of spontaneous recurrent seizures (SRS). Here, we tested the hypothesis that the A(1) receptor agonist RPia ({[}R]-N-phenylisopropyladenosine) and the A(1) antagonist DPCPX (8-Cyclopentyl-1,3-dipropylxanthine) administered to chronic pilocarpine epileptic rats would respectively decrease and increase the frequency of SRS and hippocampal excitability. Four months after Pilo-induced SE, chronic epileptic rats were video-monitored for the recording of SRS before (basal) and after a 2-week treatment with RPia (25 mu g/kg) or DPCPX (50 mu g/kg). Following sacrifice, brain slices were studied with electrophysiology. We found that rats given RPia had a 93% nonsignificant reduction in the frequency of seizures compared with their own pretreatment baseline. In contrast, the administration of DPCPX resulted in an 87% significant increase in seizure rate. Nontreated epileptic rats had a similar frequency of seizures along the study. Corroborating our behavioral data, in vitro recordings showed that slices from animals previously given DPCPX had a shorter latency to develop epileptiform activity, longer and higher DC shifts, and higher spike amplitude compared with slices from nontreated Pilo controls. In contrast, smaller spike amplitude was recorded in slices from animals given RPia. In summary, the administration of A(1) agonists reduced hippocampal excitability but not the frequency of spontaneous recurrent seizures in chronic epileptic rats, whereas A(1) receptor antagonists increased both. (C) 2016 Elsevier Inc. All rights reserved. (AU)

Processo FAPESP: 12/50950-2 - Avaliação celular dos efeitos estimulação cerebral profunda no núcleo anterior do tálamo em modelos experimentais de epilepsia do lobo temporal
Beneficiário:Luciene Covolan
Linha de fomento: Auxílio à Pesquisa - Regular
Processo FAPESP: 12/10764-5 - Avaliação celular dos efeitos estimulação cerebral profunda no núcleo anterior do tálamo em modelos experimentais de epilepsia do lobo temporal
Beneficiário:Beatriz Oliveira Amorim
Linha de fomento: Bolsas no Brasil - Doutorado Direto
Processo FAPESP: 11/50680-2 - Investigação multimodal da epileptogênese com ênfase na incorporação de novos modelos e novas ferramentas
Beneficiário:Iscia Teresinha Lopes Cendes
Linha de fomento: Auxílio à Pesquisa - Temático