Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha)
Autor(a) principal: | |
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Data de Publicação: | 1991 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0074-02761991000600034 http://repositorio.unifesp.br/handle/11600/270 |
Resumo: | Analgesic and anti-inflammatory activities of water (WE) and ethanolic (EE) extracts of Scoparia dulcis L. were investigated in rats and mice, and compared to the effects induced by Glutinol, a triterpene isolated by purification of EE. Oral adminsitration (p.o.) of either WE or EE(up to 2 g/Kg) did not alter the normal spontaneous activity of mice and rats. The sleeping time induced by sodium pentobarbital (50 mg/Kg, i.p.) was prolonged by 2 fold in mice pretreated with 0.5 g/Kg EE, p.o. Neither extract altered the tail flick response of mice in immersion test, but previous administration of EE (0.5 g/Kg, p.o.) reduced writhings induced by 0.8% acetic acid (0.1 ml/10 g, i.p.) in mice by 47% EE (0.5 and 1 g/Kg, p.o.) inhibited the paw edema induced by carrageenan in rats by respectively 46% and 58% after 2 h, being ineffective on the paw edema induced by dextran. No significant analgesic or anti-edema effects were detected in animals pretreated with WE (1 g/Kg, p.o.). Administration of Glutinol (30 mg/Kg, p.o.) reduced writhing induced by acetic acid in mice by 40% and the carrageenan induced paw edema in rats by 73%. The results indicate that the analgesic activity of S dulcis L. may be explained by explained by an anti-inflammatory activity probably related to the triterpene Glutinol. |
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Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha)Scoparia dulcis Lanalgesiaanti-inflammatorymedicinal plantAnalgesic and anti-inflammatory activities of water (WE) and ethanolic (EE) extracts of Scoparia dulcis L. were investigated in rats and mice, and compared to the effects induced by Glutinol, a triterpene isolated by purification of EE. Oral adminsitration (p.o.) of either WE or EE(up to 2 g/Kg) did not alter the normal spontaneous activity of mice and rats. The sleeping time induced by sodium pentobarbital (50 mg/Kg, i.p.) was prolonged by 2 fold in mice pretreated with 0.5 g/Kg EE, p.o. Neither extract altered the tail flick response of mice in immersion test, but previous administration of EE (0.5 g/Kg, p.o.) reduced writhings induced by 0.8% acetic acid (0.1 ml/10 g, i.p.) in mice by 47% EE (0.5 and 1 g/Kg, p.o.) inhibited the paw edema induced by carrageenan in rats by respectively 46% and 58% after 2 h, being ineffective on the paw edema induced by dextran. No significant analgesic or anti-edema effects were detected in animals pretreated with WE (1 g/Kg, p.o.). Administration of Glutinol (30 mg/Kg, p.o.) reduced writhing induced by acetic acid in mice by 40% and the carrageenan induced paw edema in rats by 73%. The results indicate that the analgesic activity of S dulcis L. may be explained by explained by an anti-inflammatory activity probably related to the triterpene Glutinol.UFMA Departamento de FisiologiaUFMA Departamento de QuímicaUSP Insituto de QuímicaEscola Paulista de Medicina Departamento de Farmacologia Setor de Produtos NaturaisUNIFESP, EPM, Depto. de Farmacologia Setor de Produtos NaturaisSciELOInstituto Oswaldo Cruz, Ministério da SaúdeUFMA Departamento de FisiologiaUFMA Departamento de QuímicaUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Freire, Sonia Maria de FariasTorres, Luce Maria Brandão [UNIFESP]Roque, Nidia FrancaSouccar, Caden [UNIFESP]Lapa, Antonio José [UNIFESP]2015-06-14T13:24:20Z2015-06-14T13:24:20Z1991-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion149-151application/pdfhttp://dx.doi.org/10.1590/S0074-02761991000600034Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 86, p. 149-151, 1991.10.1590/S0074-02761991000600034S0074-02761991000600034.pdf0074-0276S0074-02761991000600034http://repositorio.unifesp.br/handle/11600/270WOS:A1991GN58900034engMemórias do Instituto Oswaldo Cruzinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-05T21:15:17Zoai:repositorio.unifesp.br/:11600/270Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-05T21:15:17Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) |
title |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) |
spellingShingle |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) Freire, Sonia Maria de Farias Scoparia dulcis L analgesia anti-inflammatory medicinal plant |
title_short |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) |
title_full |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) |
title_fullStr |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) |
title_full_unstemmed |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) |
title_sort |
Analgesic activity of a triterpene isolated from Scoparia dulcis L. (vassourinha) |
author |
Freire, Sonia Maria de Farias |
author_facet |
Freire, Sonia Maria de Farias Torres, Luce Maria Brandão [UNIFESP] Roque, Nidia Franca Souccar, Caden [UNIFESP] Lapa, Antonio José [UNIFESP] |
author_role |
author |
author2 |
Torres, Luce Maria Brandão [UNIFESP] Roque, Nidia Franca Souccar, Caden [UNIFESP] Lapa, Antonio José [UNIFESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
UFMA Departamento de Fisiologia UFMA Departamento de Química Universidade de São Paulo (USP) Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Freire, Sonia Maria de Farias Torres, Luce Maria Brandão [UNIFESP] Roque, Nidia Franca Souccar, Caden [UNIFESP] Lapa, Antonio José [UNIFESP] |
dc.subject.por.fl_str_mv |
Scoparia dulcis L analgesia anti-inflammatory medicinal plant |
topic |
Scoparia dulcis L analgesia anti-inflammatory medicinal plant |
description |
Analgesic and anti-inflammatory activities of water (WE) and ethanolic (EE) extracts of Scoparia dulcis L. were investigated in rats and mice, and compared to the effects induced by Glutinol, a triterpene isolated by purification of EE. Oral adminsitration (p.o.) of either WE or EE(up to 2 g/Kg) did not alter the normal spontaneous activity of mice and rats. The sleeping time induced by sodium pentobarbital (50 mg/Kg, i.p.) was prolonged by 2 fold in mice pretreated with 0.5 g/Kg EE, p.o. Neither extract altered the tail flick response of mice in immersion test, but previous administration of EE (0.5 g/Kg, p.o.) reduced writhings induced by 0.8% acetic acid (0.1 ml/10 g, i.p.) in mice by 47% EE (0.5 and 1 g/Kg, p.o.) inhibited the paw edema induced by carrageenan in rats by respectively 46% and 58% after 2 h, being ineffective on the paw edema induced by dextran. No significant analgesic or anti-edema effects were detected in animals pretreated with WE (1 g/Kg, p.o.). Administration of Glutinol (30 mg/Kg, p.o.) reduced writhing induced by acetic acid in mice by 40% and the carrageenan induced paw edema in rats by 73%. The results indicate that the analgesic activity of S dulcis L. may be explained by explained by an anti-inflammatory activity probably related to the triterpene Glutinol. |
publishDate |
1991 |
dc.date.none.fl_str_mv |
1991-01-01 2015-06-14T13:24:20Z 2015-06-14T13:24:20Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0074-02761991000600034 Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 86, p. 149-151, 1991. 10.1590/S0074-02761991000600034 S0074-02761991000600034.pdf 0074-0276 S0074-02761991000600034 http://repositorio.unifesp.br/handle/11600/270 WOS:A1991GN58900034 |
url |
http://dx.doi.org/10.1590/S0074-02761991000600034 http://repositorio.unifesp.br/handle/11600/270 |
identifier_str_mv |
Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 86, p. 149-151, 1991. 10.1590/S0074-02761991000600034 S0074-02761991000600034.pdf 0074-0276 S0074-02761991000600034 WOS:A1991GN58900034 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Memórias do Instituto Oswaldo Cruz |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
149-151 application/pdf |
dc.publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268407130882048 |