In vitro antiplasmodial activity of cepharanthine

New classes of anti-malarial drugs are needed to control the alarming Plasmodium falciparum resistance toward current anti-malarial therapy. The ethnopharmacological approach allows the discovery of original chemical structures from the vegetable biodiversity. Previous studies led to the selection o...

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Veröffentlicht in:Malaria journal 2014-08, Vol.13 (1), p.327-327, Article 327
Hauptverfasser: Desgrouas, Camille, Chapus, Charles, Desplans, Jérôme, Travaille, Christelle, Pascual, Aurélie, Baghdikian, Béatrice, Ollivier, Evelyne, Parzy, Daniel, Taudon, Nicolas
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Sprache:eng
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Zusammenfassung:New classes of anti-malarial drugs are needed to control the alarming Plasmodium falciparum resistance toward current anti-malarial therapy. The ethnopharmacological approach allows the discovery of original chemical structures from the vegetable biodiversity. Previous studies led to the selection of a bisbenzylisoquinoline, called cepharanthine and isolated from a Cambodian plant: Stephania rotunda. Cepharanthine could exert a mechanism of action different from commonly used drugs. Potential plasmodial targets are reported here. To study the mechanism of action of cepharanthine, a combined approach using phenotypic and transcriptomic techniques was undertaken. Cepharanthine blocked P. falciparum development in ring stage. On a culture of synchronized ring stage, the comparisons of expression profiles showed that the samples treated with 5 μM of cepharanthine (IC90) were significantly closer to the initial controls than to the final ones. After a two-way ANOVA (p-value 
ISSN:1475-2875
1475-2875
DOI:10.1186/1475-2875-13-327