Antipyretic and anti-inflammatory properties of the ethanolic extract, dichloromethane fraction and costunolide from Magnolia ovata (Magnoliaceae)

Cândida Aparecida Leite Kassuya, Aline Cremoneze, Letícia Ferrari Lemos Barros, Alex Sandro Simas, Fernanda da Rocha Lapa, Renato Mello-Silva, Maria Élida Alves Stefanello, Aleksander Roberto Zampronio

Résultat de recherche: Articleexamen par les pairs

71 Citations (Scopus)

Résumé

Aim of the study: Magnolia ovata (A.St.-Hil.) Spreng (formerly Talauma ovata), known as "pinha-do-brejo" or "baguaçu", is a large tree widely distributed in Brazil. Its trunk bark has been used in folk medicine against fever. However, no data have been published to support the antipyretic ethnopharmacological use. This study investigated the antipyretic and anti-inflammatory effects of the ethanolic extract (EEMO), dichloromethane fraction (DCM), and the isolated compound costunolide. Materials and methods: The antipyretic and anti-inflammatory activities were evaluated in experimental models of fever and inflammation in mice. Results: The oral administration of EEMO, DCM and costunolide inhibited carrageenan (Cg)-induced paw oedema (ID50 72.35 (38.64-135.46) mg/kg, 5.8 (2.41-14.04) mg/kg and 0.18 (0.12-0.27) mg/kg, respectively) and was effective in abolishing lipopolysaccharide (LPS)-induced fever (30 mg/kg, 4.5 mg/kg and 0.15 mg/kg, respectively). EEMO was also effective in reducing cell migration in the pleurisy model. Intraplantar injection of costunolide also reduced the paw oedema, myeloperoxidase and N-acetyl-glucosaminidase activity induced by Cg in mice. Conclusions: Collectively, these results show, for the first time, that extracts obtained from Magnolia ovata possess antipyretic and anti-inflammatory properties, and costunolide appears to be the compound responsible for these effects.

Langue d'origineEnglish
Pages (de-à)369-376
Nombre de pages8
JournalJournal of Ethnopharmacology
Volume124
Numéro de publication3
DOI
Statut de publicationPublished - juill. 30 2009
Publié à l'externeOui

Note bibliographique

Funding Information:
This work was supported by grants from the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). Cândida A.L. Kassuya is a post-doctoral fellow receiving a grant from CAPES (PRODOC). A.S. Simas is a M.Sc. student supported by CAPES.

ASJC Scopus Subject Areas

  • Pharmacology
  • Drug Discovery

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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