The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)

Detalhes bibliográficos
Autor(a) principal: Rodrigues de Almeida Costa, Celso A. [UNESP]
Data de Publicação: 2011
Outros Autores: Kohn, Daniele Oliveira [UNESP], de Lima, Valeria Martins [UNESP], Gargano, Andre Costa [UNESP], Florio, Jorge Camilo, Costa, Mirtes [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.jep.2011.07.003
http://hdl.handle.net/11449/17553
Resumo: Ethnopharmacological relevance: The essential oil (EO) from Cymbopogon citratus (DC) Stapf is reported to have a wide range of biological activities and is widely used in traditional medicine as an infusion or decoction. However, despite this widely use, there are few controlled studies confirming its biological activity in central nervous system.Materials and methods: The anxiolytic-like activity of the EO was investigated in light/dark box (LDB) and marble-burying test (MBT) and the antidepressant activity was investigated in forced-swimming test (FST) in mice. Flumazenil, a competitive antagonist of benzodiazepine binding and the selective 5-HT1A receptor antagonist WAY100635 was used in experimental procedures to determine the action mechanism of EO. To exclude any false positive results in experimental procedures, mice were submitted to the rota-rod test. We also quantified some neurotransmitters at specific brain regions after EO oral acute treatment.Results: The present work found anxiolytic-like activity of the EO at the dose of 10 mg/kg in a LDB. Flumazenil, but not WAY100635, was able to reverse the effect of the EO in the LOB, indicating that the EO activity occurs via the GABA(A) receptor-benzodiazepine complex. Only at higher doses did the EO potentiate diethyl-ether-induced sleeping time in mice. In the FST and MBT, EO showed no effect. Finally, the increase in time spent in the light chamber, demonstrated by concomitant treatment with ineffective doses of diazepam (DZP) and the EO, revealed a synergistic effect of the two compounds. The lack of activity after long-term treatment in the LDB test might be related to tolerance induction, even in the DZP-treated group. Furthermore, there were no significant differences between groups after either acute or repeated treatments with the EO in the rota-rod test. Neurochemical evaluation showed no amendments in neurotransmitter levels evaluated in cortex, striatum, pons, and hypothalamus.Conclusions: The results corroborate the use of Cymbopogon citratus in folk medicine and suggest that the anxiolytic-like effect of its EO is mediated by the GABA(A) receptor-benzodiazepine complex. (C) 2011 Elsevier B.V. All rights reserved.
id UNSP_1a5d3a58b4413342b2fff0d8ec65c765
oai_identifier_str oai:repositorio.unesp.br:11449/17553
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)AnxiolyticCymbopogon citratusEssential oilGABAergic systemLemongrassSedativeEthnopharmacological relevance: The essential oil (EO) from Cymbopogon citratus (DC) Stapf is reported to have a wide range of biological activities and is widely used in traditional medicine as an infusion or decoction. However, despite this widely use, there are few controlled studies confirming its biological activity in central nervous system.Materials and methods: The anxiolytic-like activity of the EO was investigated in light/dark box (LDB) and marble-burying test (MBT) and the antidepressant activity was investigated in forced-swimming test (FST) in mice. Flumazenil, a competitive antagonist of benzodiazepine binding and the selective 5-HT1A receptor antagonist WAY100635 was used in experimental procedures to determine the action mechanism of EO. To exclude any false positive results in experimental procedures, mice were submitted to the rota-rod test. We also quantified some neurotransmitters at specific brain regions after EO oral acute treatment.Results: The present work found anxiolytic-like activity of the EO at the dose of 10 mg/kg in a LDB. Flumazenil, but not WAY100635, was able to reverse the effect of the EO in the LOB, indicating that the EO activity occurs via the GABA(A) receptor-benzodiazepine complex. Only at higher doses did the EO potentiate diethyl-ether-induced sleeping time in mice. In the FST and MBT, EO showed no effect. Finally, the increase in time spent in the light chamber, demonstrated by concomitant treatment with ineffective doses of diazepam (DZP) and the EO, revealed a synergistic effect of the two compounds. The lack of activity after long-term treatment in the LDB test might be related to tolerance induction, even in the DZP-treated group. Furthermore, there were no significant differences between groups after either acute or repeated treatments with the EO in the rota-rod test. Neurochemical evaluation showed no amendments in neurotransmitter levels evaluated in cortex, striatum, pons, and hypothalamus.Conclusions: The results corroborate the use of Cymbopogon citratus in folk medicine and suggest that the anxiolytic-like effect of its EO is mediated by the GABA(A) receptor-benzodiazepine complex. (C) 2011 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)UNESP Univ Estadual Paulista, Inst Biosci, Dept Pharmacol, BR-18618970 São Paulo, BrazilUniv São Paulo, Sch Vet Med, Dept Pathol, São Paulo, BrazilUNESP Univ Estadual Paulista, Inst Biosci, Dept Pharmacol, BR-18618970 São Paulo, BrazilFAPESP: 06/07195-8Elsevier B.V.Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Rodrigues de Almeida Costa, Celso A. [UNESP]Kohn, Daniele Oliveira [UNESP]de Lima, Valeria Martins [UNESP]Gargano, Andre Costa [UNESP]Florio, Jorge CamiloCosta, Mirtes [UNESP]2014-05-20T13:49:18Z2014-05-20T13:49:18Z2011-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article828-836application/pdfhttp://dx.doi.org/10.1016/j.jep.2011.07.003Journal of Ethnopharmacology. Clare: Elsevier B.V., v. 137, n. 1, p. 828-836, 2011.0378-8741http://hdl.handle.net/11449/1755310.1016/j.jep.2011.07.003WOS:000295236700097WOS000295236700097.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Ethnopharmacology3.1151,150info:eu-repo/semantics/openAccess2023-12-28T06:15:24Zoai:repositorio.unesp.br:11449/17553Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:29:59.670909Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
title The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
spellingShingle The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
Rodrigues de Almeida Costa, Celso A. [UNESP]
Anxiolytic
Cymbopogon citratus
Essential oil
GABAergic system
Lemongrass
Sedative
title_short The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
title_full The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
title_fullStr The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
title_full_unstemmed The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
title_sort The GABAergic system contributes to the anxiolytic-like effect of essential oil from Cymbopogon citratus (lemongrass)
author Rodrigues de Almeida Costa, Celso A. [UNESP]
author_facet Rodrigues de Almeida Costa, Celso A. [UNESP]
Kohn, Daniele Oliveira [UNESP]
de Lima, Valeria Martins [UNESP]
Gargano, Andre Costa [UNESP]
Florio, Jorge Camilo
Costa, Mirtes [UNESP]
author_role author
author2 Kohn, Daniele Oliveira [UNESP]
de Lima, Valeria Martins [UNESP]
Gargano, Andre Costa [UNESP]
Florio, Jorge Camilo
Costa, Mirtes [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Rodrigues de Almeida Costa, Celso A. [UNESP]
Kohn, Daniele Oliveira [UNESP]
de Lima, Valeria Martins [UNESP]
Gargano, Andre Costa [UNESP]
Florio, Jorge Camilo
Costa, Mirtes [UNESP]
dc.subject.por.fl_str_mv Anxiolytic
Cymbopogon citratus
Essential oil
GABAergic system
Lemongrass
Sedative
topic Anxiolytic
Cymbopogon citratus
Essential oil
GABAergic system
Lemongrass
Sedative
description Ethnopharmacological relevance: The essential oil (EO) from Cymbopogon citratus (DC) Stapf is reported to have a wide range of biological activities and is widely used in traditional medicine as an infusion or decoction. However, despite this widely use, there are few controlled studies confirming its biological activity in central nervous system.Materials and methods: The anxiolytic-like activity of the EO was investigated in light/dark box (LDB) and marble-burying test (MBT) and the antidepressant activity was investigated in forced-swimming test (FST) in mice. Flumazenil, a competitive antagonist of benzodiazepine binding and the selective 5-HT1A receptor antagonist WAY100635 was used in experimental procedures to determine the action mechanism of EO. To exclude any false positive results in experimental procedures, mice were submitted to the rota-rod test. We also quantified some neurotransmitters at specific brain regions after EO oral acute treatment.Results: The present work found anxiolytic-like activity of the EO at the dose of 10 mg/kg in a LDB. Flumazenil, but not WAY100635, was able to reverse the effect of the EO in the LOB, indicating that the EO activity occurs via the GABA(A) receptor-benzodiazepine complex. Only at higher doses did the EO potentiate diethyl-ether-induced sleeping time in mice. In the FST and MBT, EO showed no effect. Finally, the increase in time spent in the light chamber, demonstrated by concomitant treatment with ineffective doses of diazepam (DZP) and the EO, revealed a synergistic effect of the two compounds. The lack of activity after long-term treatment in the LDB test might be related to tolerance induction, even in the DZP-treated group. Furthermore, there were no significant differences between groups after either acute or repeated treatments with the EO in the rota-rod test. Neurochemical evaluation showed no amendments in neurotransmitter levels evaluated in cortex, striatum, pons, and hypothalamus.Conclusions: The results corroborate the use of Cymbopogon citratus in folk medicine and suggest that the anxiolytic-like effect of its EO is mediated by the GABA(A) receptor-benzodiazepine complex. (C) 2011 Elsevier B.V. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-09-01
2014-05-20T13:49:18Z
2014-05-20T13:49:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.jep.2011.07.003
Journal of Ethnopharmacology. Clare: Elsevier B.V., v. 137, n. 1, p. 828-836, 2011.
0378-8741
http://hdl.handle.net/11449/17553
10.1016/j.jep.2011.07.003
WOS:000295236700097
WOS000295236700097.pdf
url http://dx.doi.org/10.1016/j.jep.2011.07.003
http://hdl.handle.net/11449/17553
identifier_str_mv Journal of Ethnopharmacology. Clare: Elsevier B.V., v. 137, n. 1, p. 828-836, 2011.
0378-8741
10.1016/j.jep.2011.07.003
WOS:000295236700097
WOS000295236700097.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Ethnopharmacology
3.115
1,150
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 828-836
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808129326550351872