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Antimicrob. Agents Chemother., 11 1997, 2533-2539, Vol 41, No. 11
G Francois, G Timperman, W Eling, LA Assi, J Holenz and G Bringmann
Naphthylisoquinoline alkaloid-containing extracts from species of the
families Dioncophyllaceae and Ancistrocladaceae and purified alkaloids
derived therefrom were shown to exhibit antiparasitic activity in
Plasmodium berghei-infected mice. Several extracts and alkaloids,
especially dioncophylline C and dioncopeltine A, isolated from
Triphyophyllum peltatum (Dioncophyllaceae), displayed high levels of
activity. Dioncopeltine A was able to suppress parasitemia almost totally,
while dioncophylline C cured infected mice completely after oral treatment
with 50 mg kg of body weight(-1) day(-1) for 4 days without noticeable
toxic effects. Analysis of the dose-response relationship of dioncophylline
C revealed a 50% effective dosage (ED50) of 10.71 mg kg(-1) day(-1) under
these conditions. Although four daily treatments with 50 mg kg(-1) day(-1)
are needed to achieve radical cure, one oral dose is sufficient to kill
99.6% of the parasites. Intravenous application of dioncophylline C is even
more effective, with an ED50 of 1.90 mg kg(-1) day(-1) and no noticeable
toxic effects. The compound also suppressed more established P. berghei
infections when orally applied at day 3 after infection. Both dioncopeltine
A and dioncophylline C are active against the chloroquine-resistant P.
berghei Anka CRS parasites. Sustained release of these compounds at 20 mg
kg(-1) day(-1) by implanted miniosmotic pumps exhibited curative effects.
The naphthylisoquinoline alkaloids are therefore promising new antimalarial
agents.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Naphthylisoquinoline alkaloids against malaria: evaluation of the curative potentials of dioncophylline C and dioncopeltine A against Plasmodium berghei in vivo
Prins Leopold Instituut voor Tropische Geneeskunde, Antwerp, Belgium.
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