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Volume 17, Issue 5, Pages 375-378 (April 2010)


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Antileishmanial activity of furoquinolines and coumarins from Helietta apiculata

Maria Elena Ferreiraa, Antonieta Rojas de Ariasb, Gloria Yaluffa, Ninfa Vera de Bilbaoa, Hector Nakayamaa, Susana Torresa, Alicia Schininia, Isabelle Guyc, Horacio Heinzend, Alain FourneteCorresponding Author Informationemail address

published online 30 October 2009.

Abstract 

The bark infusion of H. apiculata are used to treat wound healing related to cutaneous leishmaniasis and as anti-inflammatory.

Aim of the study

To isolate, purify active constituents of H. apiculata stem bark, and evaluate their in vitro and in vivo antileishmanial activities.

Materials and methods

Isolation by chromatographic methods and chemical identification of furoquinoline alkaloids and coumarins, then evaluation of the in vitro leishmanicidal activity of these compounds against three strains of Leishmania sp. promastigotes and in vivo against Leishmania amazonensis in Balb/c mice.

Results

Furoquinoline alkaloids and coumarins presented a moderate in vitro activity against promastigote forms of Leishmania sp. with IC50 values in the range between 17 and >50μg/ml. Balb/c mice infected with Leishmania amazonensis were treated with γ-fagarine by oral route, or with 3-(1’-dimethylallyl)-decursinol or (-)-heliettin by subscutaneous route for 14 days at 10mg/kg daily. In these conditions, γ-fagarine, 3-(1’-dimethylallyl)-decursinol and (-)-heliettin showed the same efficacy as the reference drug reducing by 97.4, 95.6 and 98.6% the parasite loads in the lesion, respectively.

Conclusion

These compounds showed significant efficacy in L. amazonensis infected mice, providing important knowledge to improve its potential role for a future use in the treatment of cutaneous leishmaniasis.

a Instituto de Investigaciones en Ciencias de la Salud, Department of Tropical Medicine, Asunción, Paraguay

b Centro para el Desarrollo de la Investigación Científica (CEDIC/FMB/Diaz Gill Medicina Laboratorial), Asunción, Paraguay

c Substances d’Origine Naturelle et Analogues Structuraux, Faculté de Pharmacie, Université d’Angers, Angers, France

d Cátedra de Farmacognosia y Productos Naturales, Facultad de Química, Montevideo, Uruguay

e IRD US 084, Laboratoire de Pharmacognosie, Faculté de Pharmacie, rue J.B. Clément, 92296 Châtenay-Malabry cedex, France

Corresponding Author InformationCorresponding author. Tel.: +330146835969; fax: +330146835399.

PII: S0944-7113(09)00238-4

doi:10.1016/j.phymed.2009.09.009


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