Monoterpenoid Terpinen-4-ol exhibits anticonvulsant activity in behavioural and electrophysiological studies.

• Autor(a) principal: NÓBREGA, Franklin Ferreira de Farias.
• Data de Publicação: 2014
• Outros Autores: SALVADORI, Mirian Graciela da Silva Stiebbe., MASSON, Cintia Junia., MELLO, Carlos Fernando de., SANTOS-NASCIMENTO, T., LEAL-CARDOSO, Jose Henrique, SOUSA, Damião Pergentino de., ALMEIDA, Reinaldo Nobrega de.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Biblioteca Digital de Teses e Dissertações da UFCG
• Texto Completo: http://dspace.sti.ufcg.edu.br:8080/jspui/handle/riufcg/37246
• topic: Monoterpenoid Terpinen-4-ol; Psychopharmacological - 4TRP; Electrophysiological activities - 4TRP; Central nervous system; Anticonvulsant activity; Psicofarmacológico - 4TRP; Atividades eletrofisiológicas - 4TRP; Sistema nervoso central; Atividade anticonvulsivante; Farmácia.; Química.

Terpinen-4-ol (4TRP) is a monoterpenoid alcoholic component of essential oils obtained from several aromatic plants. We investigated the psychopharmacological and electrophysiological activities of 4TRP in male Swiss mice and Wistar rats. 4TRP was administered intraperitoneally (i.p.) at doses of 25 to 200 mg/kg and intracerebroventricularly (i.c.v.) at concentrations of 10, 20, and 40 ng/2 μL. For in vitro experiments, 4TRP concentrations were 0.1 mM and 1.0 mM. 4TRP (i.p.) inhibited pentylenetetrazol- (PTZ-) induced seizures, indicating anticonvulsant effects. Electroencephalographic recordings showed that 4TRP (i.c.v.) protected against PTZ-induced seizures, corroborating the behavioural results. To determine whether 4TRP exerts anticonvulsant effects via regulation of GABAergic neurotransmission, we measured convulsions induced by 3-mercapto-propionic acid (3-MP). The obtained results showed involvement of the GABAergic system in the anticonvulsant action exerted by 4TRP, but flumazenil, a selective antagonist of the benzodiazepine site of the GABAA receptor, did not reverse the anticonvulsant effect, demonstrating that 4TRP does not bind to the benzodiazepine-binding site. Furthermore, 4TRP decreased the sodium current through voltage-dependent sodium channels, and thus its anticonvulsant effect may be related to changes in neuronal excitability because of modulation of these channels.