Planta Med 2011; 77(10): 1035-1043
DOI: 10.1055/s-0030-1250745
Natural Product Chemistry
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

A New Naphthoquinone Isolated from the Bulbs of Cipura paludosa and Pharmacological Activity of Two Main Constituents

Priscila Batista Tessele1 , Franco Delle Monache1 , Nara Lins Meira Quintão1 , Gislaine Francieli da Silva1 , Lilian Wunsch Rocha1 , Greice M. R. S. Lucena2 , Vania M. M. Ferreira2 , Rui D. S. Prediger3 , Valdir Cechinel Filho1
  • 1Núcleo de Investigações Químico-Farmacêuticas (NIQFAR) and Programa de Mestrado em Ciências Farmacêuticas, Universidade do Vale do Itajaí (UNIVALI), Itajaí, SC, Brazil
  • 2Faculdade de Ciências da Saúde, Curso de Ciências Farmacêuticas, Universidade de Brasília (UnB), Brasília, DF, Brazil
  • 3Departamento de Farmacologia, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina (UFSC), Florianópolis, SC, Brazil
Further Information

Publication History

received April 6, 2010 revised Nov. 4, 2010

accepted Dec. 17, 2010

Publication Date:
31 January 2011 (online)

Abstract

Cipura paludosa (Iridaceae) is a plant that is distributed in the north region of Brazil. Its bulbs are used in folk medicine to treat inflammation and pain. Four naphthalene derivatives have been isolated from the bulbs of this plant. Three of them have been identified as the known naphthalene derivatives, eleutherine, iso-eleutherine, and hongkonin. The structure of the fourth and new component was determined as 11-hydroxyeleutherine by extensive NMR study. In addition, the in vivo effect of the two major compounds, eleutherine and iso-eleutherine, was evaluated in carrageenan-induced hypernociception and inflammation in mice. Eleutherine and iso-eleutherine (1.04–34.92 µmol/kg), dosed intraperitoneally (i. p.) or orally (p. o.), decreased the carrageenan-induced paw oedema (i. p. – inhibitions of 36 ± 7 % and 58 ± 14 %, respectively; p. o. – inhibitions of 36 ± 7 % and 58 ± 14 %, respectively). Iso-eleutherine, but not eleutherine, significantly reduced (inhibitions of 39 ± 4 %) the plasma extravasation induced by intradermal (i. d.) injection of carrageenan. Likewise, eleutherine and iso-eleutherine (1.04–34.92 µmol/kg, i. p. or p. o.) were also effective in preventing the carrageenan-induced hypernociceptive response (i. p. – inhibition of 59 ± 4 % and 63 ± 1 %, respectively; p. o. – inhibitions of 36 ± 7 % and 58 ± 14 %, respectively). It was also suggested that the anti-inflammatory and anti-hypernociceptive effects of eleutherine or iso-eleutherine partly depend on the interference with the synthesis or activity of mast cell products, kinins, cytokine, chemokines, prostanoids, or sympathetic amines. Our findings show that two major compounds of C. paludosa contain pharmacologically active constituents that possess antinociceptive and anti-inflammatory activity, justifying, at least in part, its popular therapeutic use for treating conditions associated with pain.

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Prof. Dr. Valdir Cechinel Filho

Núcleo de Investigações Químico-Farmacêuticas (NIQFAR) and Programa de Mestrado em Ciências Farmacêuticas
Universidade do Vale do Itajaí (UNIVALI)

Rua Uruguai, 458

88302-202 Itajaí SC

Brazil

Phone: +55 47 33 41 76 64

Fax: +55 47 33 41 76 01

Email: cechinel@univali.br

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