Antimalarial action of hydroxamate-based iron chelators and potentiation of desferrioxamine action by reversed siderophores

J. Golenser, A. Tsafack, Y. Amichai, J. Libman, A. Shanzer, Z. I. Cabantchik*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

Hydroxamate-based chelators of iron are potent inhibitors of in vitro growth of Plasmodium falciparum. Two types of such chelators, the natural desferrioxamine and the synthetic reversed siderophore RSF(ileum 2), are prototypes of antimalarial agents whose action spectra differ in the speed of action, stage dependence, and degree of reversibility of effects. This work explores the possibility of improving the antimalarial efficacy of these agents by using them in various combinations on in vitro cultures of P. falciparum. Growth assessment was based both on total nucleic acid synthesis and on parasitemia. The results indicate that the synthetic reversed siderophore more than complements the antimalarial action of desferrioxamine when applied during either ring, trophozoite, or mixed stages. The combined drug effects were significantly higher than the additive effect of the individual drugs. Qualitatively similar results were obtained for both reversible effects and irreversible (i.e., sustained) effects. Following an 8-h window of exposure the combined drug treatment caused parasite growth arrest and prevented its recovery, even 3 days after the treatment. The fact that such a combination of iron chelators displays a wider action spectrum than either drug alone has implications for the design of chemotherapy regimens.

Original languageEnglish
Pages (from-to)61-65
Number of pages5
JournalAntimicrobial Agents and Chemotherapy
Volume39
Issue number1
DOIs
StatePublished - 1995

Fingerprint

Dive into the research topics of 'Antimalarial action of hydroxamate-based iron chelators and potentiation of desferrioxamine action by reversed siderophores'. Together they form a unique fingerprint.

Cite this