Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves

Detalhes bibliográficos
Autor(a) principal: Branquinho, Lidiane Schultz
Data de Publicação: 2017
Outros Autores: Santos, Joyce Alencar, Cardoso, Claudia Andrea Lima, Mota, Jonas da Silva, Junior, Ubirajara Lanza, Kassuya, Cândida Aparecida Leite, Arena, Arielle Cristina [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.jep.2017.01.008
http://hdl.handle.net/11449/174140
Resumo: Ethnopharmacological relevance Although some of the species of the genus Piper exhibit interesting biological properties, studies on Piper glabratum Kunth are very limited. Aim of the study This study investigated the anti-inflammatory activity and the toxicological profile of the essential oil from P. glabratum leaves (OEPG) in mice. Materials and Methods The acute toxicity of OEPG was evaluated by oral administration to female mice as single doses of 500, 1000, 2000 or 5000 mg/kg/body weight. In the subacute toxicity test, the females received 500 or 1000 mg/kg/body weight of OEPG for 28 days. The anti-inflammatory potential of OEPG was evaluated using four models including pleurisy, edema, mechanical hyperalgesia and cold allodynia models in mouse paws. Results No clinical signs of toxicity were observed in animals after acute treatment, which suggested that the LD50 is greater than 5000 mg/kg. The subacute exposure to OEPG produced no significant changes in the hematological or biochemical parameters. Similarly, the histology of the organs and the estrus cycle displayed no marked alterations. OEPG exhibited anti-inflammatory activity as indicated by inhibition of the leukocyte migration (100, 300, 700 mg/kg) and the protein extravasation into the pleural exudates (700 mg/kg). After intraplantar injection of carrageenan, it was observed that the 700 mg/kg dose of OEPG reduced edema formation and decreased the sensitivity to mechanical stimulation and cold. Conclusions These results demonstrate the anti-inflammatory potential of the essential oil of P. glabratum leaves in the absence of toxicity in female mice.
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spelling Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leavesCarrageenanEssential oilInflammationPiper glabratumToxicityEthnopharmacological relevance Although some of the species of the genus Piper exhibit interesting biological properties, studies on Piper glabratum Kunth are very limited. Aim of the study This study investigated the anti-inflammatory activity and the toxicological profile of the essential oil from P. glabratum leaves (OEPG) in mice. Materials and Methods The acute toxicity of OEPG was evaluated by oral administration to female mice as single doses of 500, 1000, 2000 or 5000 mg/kg/body weight. In the subacute toxicity test, the females received 500 or 1000 mg/kg/body weight of OEPG for 28 days. The anti-inflammatory potential of OEPG was evaluated using four models including pleurisy, edema, mechanical hyperalgesia and cold allodynia models in mouse paws. Results No clinical signs of toxicity were observed in animals after acute treatment, which suggested that the LD50 is greater than 5000 mg/kg. The subacute exposure to OEPG produced no significant changes in the hematological or biochemical parameters. Similarly, the histology of the organs and the estrus cycle displayed no marked alterations. OEPG exhibited anti-inflammatory activity as indicated by inhibition of the leukocyte migration (100, 300, 700 mg/kg) and the protein extravasation into the pleural exudates (700 mg/kg). After intraplantar injection of carrageenan, it was observed that the 700 mg/kg dose of OEPG reduced edema formation and decreased the sensitivity to mechanical stimulation and cold. Conclusions These results demonstrate the anti-inflammatory potential of the essential oil of P. glabratum leaves in the absence of toxicity in female mice.School of Health Sciences Federal University of Grande DouradosMato Grosso do Sul State University (UEMS)Department of Morphology Institute of Biosciences of Botucatu UNESP – Univ. Estadual PaulistaDepartment of Morphology Institute of Biosciences of Botucatu UNESP – Univ. Estadual PaulistaFederal University of Grande DouradosUniversidade Estadual de Mato Grosso do Sul (UEMS)Universidade Estadual Paulista (Unesp)Branquinho, Lidiane SchultzSantos, Joyce AlencarCardoso, Claudia Andrea LimaMota, Jonas da SilvaJunior, Ubirajara LanzaKassuya, Cândida Aparecida LeiteArena, Arielle Cristina [UNESP]2018-12-11T17:09:31Z2018-12-11T17:09:31Z2017-02-23info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article372-378http://dx.doi.org/10.1016/j.jep.2017.01.008Journal of Ethnopharmacology, v. 198, p. 372-378.1872-75730378-8741http://hdl.handle.net/11449/17414010.1016/j.jep.2017.01.0082-s2.0-85010880298Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Ethnopharmacology1,150info:eu-repo/semantics/openAccess2021-10-23T16:16:18Zoai:repositorio.unesp.br:11449/174140Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T16:16:18Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
title Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
spellingShingle Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
Branquinho, Lidiane Schultz
Carrageenan
Essential oil
Inflammation
Piper glabratum
Toxicity
title_short Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
title_full Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
title_fullStr Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
title_full_unstemmed Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
title_sort Anti-inflammatory and toxicological evaluation of essential oil from Piper glabratum leaves
author Branquinho, Lidiane Schultz
author_facet Branquinho, Lidiane Schultz
Santos, Joyce Alencar
Cardoso, Claudia Andrea Lima
Mota, Jonas da Silva
Junior, Ubirajara Lanza
Kassuya, Cândida Aparecida Leite
Arena, Arielle Cristina [UNESP]
author_role author
author2 Santos, Joyce Alencar
Cardoso, Claudia Andrea Lima
Mota, Jonas da Silva
Junior, Ubirajara Lanza
Kassuya, Cândida Aparecida Leite
Arena, Arielle Cristina [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Federal University of Grande Dourados
Universidade Estadual de Mato Grosso do Sul (UEMS)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Branquinho, Lidiane Schultz
Santos, Joyce Alencar
Cardoso, Claudia Andrea Lima
Mota, Jonas da Silva
Junior, Ubirajara Lanza
Kassuya, Cândida Aparecida Leite
Arena, Arielle Cristina [UNESP]
dc.subject.por.fl_str_mv Carrageenan
Essential oil
Inflammation
Piper glabratum
Toxicity
topic Carrageenan
Essential oil
Inflammation
Piper glabratum
Toxicity
description Ethnopharmacological relevance Although some of the species of the genus Piper exhibit interesting biological properties, studies on Piper glabratum Kunth are very limited. Aim of the study This study investigated the anti-inflammatory activity and the toxicological profile of the essential oil from P. glabratum leaves (OEPG) in mice. Materials and Methods The acute toxicity of OEPG was evaluated by oral administration to female mice as single doses of 500, 1000, 2000 or 5000 mg/kg/body weight. In the subacute toxicity test, the females received 500 or 1000 mg/kg/body weight of OEPG for 28 days. The anti-inflammatory potential of OEPG was evaluated using four models including pleurisy, edema, mechanical hyperalgesia and cold allodynia models in mouse paws. Results No clinical signs of toxicity were observed in animals after acute treatment, which suggested that the LD50 is greater than 5000 mg/kg. The subacute exposure to OEPG produced no significant changes in the hematological or biochemical parameters. Similarly, the histology of the organs and the estrus cycle displayed no marked alterations. OEPG exhibited anti-inflammatory activity as indicated by inhibition of the leukocyte migration (100, 300, 700 mg/kg) and the protein extravasation into the pleural exudates (700 mg/kg). After intraplantar injection of carrageenan, it was observed that the 700 mg/kg dose of OEPG reduced edema formation and decreased the sensitivity to mechanical stimulation and cold. Conclusions These results demonstrate the anti-inflammatory potential of the essential oil of P. glabratum leaves in the absence of toxicity in female mice.
publishDate 2017
dc.date.none.fl_str_mv 2017-02-23
2018-12-11T17:09:31Z
2018-12-11T17:09:31Z
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.2017.01.008
Journal of Ethnopharmacology, v. 198, p. 372-378.
1872-7573
0378-8741
http://hdl.handle.net/11449/174140
10.1016/j.jep.2017.01.008
2-s2.0-85010880298
url http://dx.doi.org/10.1016/j.jep.2017.01.008
http://hdl.handle.net/11449/174140
identifier_str_mv Journal of Ethnopharmacology, v. 198, p. 372-378.
1872-7573
0378-8741
10.1016/j.jep.2017.01.008
2-s2.0-85010880298
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Ethnopharmacology
1,150
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 372-378
dc.source.none.fl_str_mv Scopus
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
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