Attenuation of capsaicin-induced acute and visceral nociceptive pain by a - and h -amyrin, a triterpene mixture isolated from Protium heptaphyllum resin in mice
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , , , , , , , |
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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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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1813029036079710208 |