Acute and topic anti-edematogenic fractions isolated from the seeds of Pterodon pubescens

Author:

Silva M C C1,Gayer C R M1,Lopes C S1,Calixto N O1,Reis P A1,Passaes C P B1,Paes M C1,Dalmau S R12,Sabino K C C1,Todeschini A R1,Coelho M G P1

Affiliation:

1. Departamento de Bioquímica, Instituto de Biologia, Universidade do Estado do Rio de Janeiro, Av Professor Manoel de Abreu, 44, PAPC, 4° andar, CEP 20550-170, Rio de Janeiro, RJ, Brazil

2. Division of Experimental Medicine, Research Division, National Cancer Institute, Praça Cruz Vermelha 23, 6° andar, CEP 20230-130, Rio de Janerio, RJ, Brazil

Abstract

Abstract We previously demonstrated that alcoholic extracts from Pterodon pubescens Benth. (Sucupira branca, Leguminosae) seeds exhibit anti-arthritic activity. In the present work we show that the oleaginous extract obtained from P. pubescens seeds (OEP) exhibits acute or topic anti-edematogenic activity when tested in carrageenan-induced paw edema or in croton oil-induced ear edema assays, respectively. Four fractions were obtained from OEP by sequential liquid–liquid extraction. The anti-edematogenic properties were predominant in the hexanic fraction, which was further fractionated by HPLC, yielding three sub-fractions (PF1.1, PF1.2 and PF1.3). PF1.1 and PF1.3 showed potent acute and topic anti-edematogenic activity. The PF1.2 sub-fraction, although not active in the carrageenan assay, exhibited a potent anti-edematogenic activity in the croton oil-induced ear edema. This sub-fraction shows a maximum efficacy similar to indometacin in a lower dose. The PF1.1 sub-fraction presented a complex mixture containing furane diterpene derivatives of vouacapan. PF1.2 consists of a single substance, geranylgeraniol, as determined by GC/MS and NMR, while PF1.3 contains farnesol.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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