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Evaluation of central nervous system effects of Citrus limon essential oil in mice
Campêlo, Lidianne Mayra Lopes; Lima, Sidney Gonçalo de; Feitosa, Chistiane Mendes; Freitas, Rivelilson Mendes de.
  • Campêlo, Lidianne Mayra Lopes; Universidade Federal do Piauí. Programa de Pós-graduação em Ciências Farmacêuticas Núcleo de Tecnologia Farmacêutica. Laboratório de Pesquisa em Neuroquímica Experimental. BR
  • Lima, Sidney Gonçalo de; Universidade Federal do Piauí. Departamento de Química. BR
  • Feitosa, Chistiane Mendes; Universidade Federal do Piauí. Programa de Pós-graduação em Ciências Farmacêuticas Núcleo de Tecnologia Farmacêutica. Laboratório de Pesquisa em Neuroquímica Experimental. BR
  • Freitas, Rivelilson Mendes de; Universidade Federal do Piauí. Programa de Pós-graduação em Ciências Farmacêuticas Núcleo de Tecnologia Farmacêutica. Laboratório de Pesquisa em Neuroquímica Experimental. BR
Rev. bras. farmacogn ; 21(4): 668-673, jul.-ago. 2011. ilus, tab
Article in English | LILACS | ID: lil-596239
ABSTRACT
The central nervous system (CNS) depressant and anticonvulsant activities of Citrus limon (L.) Osbeck, Rutaceae, essential oil (EO) were investigated in animal models. The EO (50, 100 and 150 mg/kg) injected by oral route (p.o.) in mice caused a significant decrease in the motor activity of animals when compared with the control group, up to thirty days after the administration and the dose of 150 mg/kg significantly reduced the remaining time of the animals on the Rota-rod apparatus. Additionally, C. limon essential oil was also capable to promote an increase of latency for development of convulsions induced by pentylenetetrazole (PTZ). The administration of FLU (10 mg/kg, i.p.), GABA A-benzodiazepine (GABA-BZD) receptor antagonist, antagonized the effect of C. limon essential oil at higher dose. This C. limon essential oil was also capable to promote an increase of latency for development of convulsions induced by picrotoxin (PIC) at higher dose. In the same way, the anticonvulsant effect of the EO was affected by pretreatment with flumazenil, a selective antagonist of benzodiazepine site of GABA A receptor. These results suggest a possible CNS depressant and anticonvulsant activities in mice that needs further investigation.


Full text: Available Index: LILACS (Americas) Language: English Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 2011 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Piauí/BR

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Full text: Available Index: LILACS (Americas) Language: English Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 2011 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Piauí/BR