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Potentiation of the antimalarial agent rufigallol
Author(s) -
Rolf W. Winter,
Ken Cornell,
Linda L. Johnson,
Marina Ignatushchenko,
David J. Hinrichs,
Michael K. Riscoe
Publication year - 1996
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.40.6.1408
Subject(s) - chloroquine , long term potentiation , plasmodium falciparum , antimalarial agent , pharmacology , biology , radical , chemistry , drug , malaria , stereochemistry , biochemistry , immunology , receptor
We have discovered a remarkable synergistic antimalarial interaction between rufigallol and the structurally similar compound exifone. The synergistic effects were produced in chloroquine-susceptible and chloroquine-resistant clones of Plasmodium falciparum. The degree of potentiation as estimated by standard isobolar analysis was approximately 60-fold for experiments initiated with asynchronous parasites. The most pronounced synergism was observed in experiments with synchronized trophozoite-infected erythrocytes, in which the degree of synergy was at least 300-fold. While the mechanism underlying this drug potentiation remains unresolved, it is hypothesized that rufigallol acts in pro-oxidant fashion to produce oxygen radicals inside parasitized erythrocytes. These radicals would attack exifone, thereby initiating its transformation into a more potent compound, a xanthone.

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