Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice

Detalhes bibliográficos
Autor(a) principal: Oliveira, Francisco A.
Data de Publicação: 2005
Outros Autores: Costa, Charllynton L.S., Chaves, Mariana H.0, Almeida, Fernanda Regina de Castro, Cavalcante, Ítalo José Mesquita, Lima, Alana Fonteles, Lima Jr., Roberto César Pereira, Silva, Regilane M., Campos, Adriana Rolim, Santos, Flavia Almeida, Rao, Vietla Satyanarayana
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
Texto Completo: http://www.repositorio.ufc.br/handle/riufc/5603
Resumo: The triterpene mixture, a - and h -amyrin, isolated from Protium heptaphyllum resin was evaluated on capsaicin- evoked nociception in mice. Orally administered a - and h -amyrin (3 to 100 mg/kg) significantly suppressed the nociceptive behaviors—evoked by either subplantar (1.6 A g) or intracolonic (149 A g) application of capsaicin. The antinociception produced by a - and h -amyrin against subplantar capsaicin-induced paw-licking behavior was neither potentiated nor attenuated by ruthenium red (1.5 mg/kg, s.c.), a non-specific antagonist of vanilloid receptor (TRPV1), but was greatly abolished in animals pretreated with naloxone (2 mg/kg, s.c.), suggesting an opioid mechanism. However, participation of a 2 -adrenoceptor involvement was unlikely since yohimbine (2 mg/ kg, i.p.) pretreatment failed to block the antinociceptive effect of a - and h -amyrin in the experimental model of visceral nociception evoked by intracolonic capsaicin. The triterpene mixture (3 to 30 mg/kg, p.o.) neither altered significantly the pentobarbital sleeping time, nor impaired the ambulation or motor coordination in open-field and rota-rod tests, respectively, indicating the absence of sedative or motor abnormality that could account for its antinociception. Nevertheless, a - and h -amyrin could significantly block the capsaicin (10 mg/kg, s.c.)-induced
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spelling Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in miceCapsaicinaRatosThe triterpene mixture, a - and h -amyrin, isolated from Protium heptaphyllum resin was evaluated on capsaicin- evoked nociception in mice. Orally administered a - and h -amyrin (3 to 100 mg/kg) significantly suppressed the nociceptive behaviors—evoked by either subplantar (1.6 A g) or intracolonic (149 A g) application of capsaicin. The antinociception produced by a - and h -amyrin against subplantar capsaicin-induced paw-licking behavior was neither potentiated nor attenuated by ruthenium red (1.5 mg/kg, s.c.), a non-specific antagonist of vanilloid receptor (TRPV1), but was greatly abolished in animals pretreated with naloxone (2 mg/kg, s.c.), suggesting an opioid mechanism. However, participation of a 2 -adrenoceptor involvement was unlikely since yohimbine (2 mg/ kg, i.p.) pretreatment failed to block the antinociceptive effect of a - and h -amyrin in the experimental model of visceral nociception evoked by intracolonic capsaicin. The triterpene mixture (3 to 30 mg/kg, p.o.) neither altered significantly the pentobarbital sleeping time, nor impaired the ambulation or motor coordination in open-field and rota-rod tests, respectively, indicating the absence of sedative or motor abnormality that could account for its antinociception. Nevertheless, a - and h -amyrin could significantly block the capsaicin (10 mg/kg, s.c.)-inducedLife Sciences2013-08-12T12:37:39Z2013-08-12T12:37:39Z2005-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfOLIVEIRA, F. A. et al. Attenuation of capsaicin-induced acute and visceral nociceptive pain by a-and h-amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice. Life Sciences, Elmsford, NY, v. 77, n. 23, p. 2942-2952, maio, 2005.0024-3205http://www.repositorio.ufc.br/handle/riufc/5603Oliveira, Francisco A.Costa, Charllynton L.S.Chaves, Mariana H.0Almeida, Fernanda Regina de CastroCavalcante, Ítalo José MesquitaLima, Alana FontelesLima Jr., Roberto César PereiraSilva, Regilane M.Campos, Adriana RolimSantos, Flavia AlmeidaRao, Vietla Satyanarayanaengreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2022-05-31T13:49:58Zoai:repositorio.ufc.br:riufc/5603Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T19:01:19.855287Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
title Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
spellingShingle Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
Oliveira, Francisco A.
Capsaicina
Ratos
title_short Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
title_full Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
title_fullStr Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
title_full_unstemmed Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
title_sort Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
author Oliveira, Francisco A.
author_facet Oliveira, Francisco A.
Costa, Charllynton L.S.
Chaves, Mariana H.0
Almeida, Fernanda Regina de Castro
Cavalcante, Ítalo José Mesquita
Lima, Alana Fonteles
Lima Jr., Roberto César Pereira
Silva, Regilane M.
Campos, Adriana Rolim
Santos, Flavia Almeida
Rao, Vietla Satyanarayana
author_role author
author2 Costa, Charllynton L.S.
Chaves, Mariana H.0
Almeida, Fernanda Regina de Castro
Cavalcante, Ítalo José Mesquita
Lima, Alana Fonteles
Lima Jr., Roberto César Pereira
Silva, Regilane M.
Campos, Adriana Rolim
Santos, Flavia Almeida
Rao, Vietla Satyanarayana
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Oliveira, Francisco A.
Costa, Charllynton L.S.
Chaves, Mariana H.0
Almeida, Fernanda Regina de Castro
Cavalcante, Ítalo José Mesquita
Lima, Alana Fonteles
Lima Jr., Roberto César Pereira
Silva, Regilane M.
Campos, Adriana Rolim
Santos, Flavia Almeida
Rao, Vietla Satyanarayana
dc.subject.por.fl_str_mv Capsaicina
Ratos
topic Capsaicina
Ratos
description The triterpene mixture, a - and h -amyrin, isolated from Protium heptaphyllum resin was evaluated on capsaicin- evoked nociception in mice. Orally administered a - and h -amyrin (3 to 100 mg/kg) significantly suppressed the nociceptive behaviors—evoked by either subplantar (1.6 A g) or intracolonic (149 A g) application of capsaicin. The antinociception produced by a - and h -amyrin against subplantar capsaicin-induced paw-licking behavior was neither potentiated nor attenuated by ruthenium red (1.5 mg/kg, s.c.), a non-specific antagonist of vanilloid receptor (TRPV1), but was greatly abolished in animals pretreated with naloxone (2 mg/kg, s.c.), suggesting an opioid mechanism. However, participation of a 2 -adrenoceptor involvement was unlikely since yohimbine (2 mg/ kg, i.p.) pretreatment failed to block the antinociceptive effect of a - and h -amyrin in the experimental model of visceral nociception evoked by intracolonic capsaicin. The triterpene mixture (3 to 30 mg/kg, p.o.) neither altered significantly the pentobarbital sleeping time, nor impaired the ambulation or motor coordination in open-field and rota-rod tests, respectively, indicating the absence of sedative or motor abnormality that could account for its antinociception. Nevertheless, a - and h -amyrin could significantly block the capsaicin (10 mg/kg, s.c.)-induced
publishDate 2005
dc.date.none.fl_str_mv 2005-05
2013-08-12T12:37:39Z
2013-08-12T12:37:39Z
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 OLIVEIRA, F. A. et al. Attenuation of capsaicin-induced acute and visceral nociceptive pain by a-and h-amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice. Life Sciences, Elmsford, NY, v. 77, n. 23, p. 2942-2952, maio, 2005.
0024-3205
http://www.repositorio.ufc.br/handle/riufc/5603
identifier_str_mv OLIVEIRA, F. A. et al. Attenuation of capsaicin-induced acute and visceral nociceptive pain by a-and h-amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice. Life Sciences, Elmsford, NY, v. 77, n. 23, p. 2942-2952, maio, 2005.
0024-3205
url http://www.repositorio.ufc.br/handle/riufc/5603
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Life Sciences
publisher.none.fl_str_mv Life Sciences
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
instacron_str UFC
institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
collection Repositório Institucional da Universidade Federal do Ceará (UFC)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)
repository.mail.fl_str_mv bu@ufc.br || repositorio@ufc.br
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