Growth Inhibition of Plasmodium Falciparum Involving Carbon Centered Iron-Chelate Radical (L., X-)-Fe(III) Based on Pyridoxal-Betaine. A Novel Type of Antimalarials Active Against Chloroquine-Resistant Parasites |
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Authors: | Eugene N. Iheanacho Shalom Sarel Amram Samuni Schelly Avramovici-grisaru Dan T. Spira |
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Affiliation: | a The Kuvin Centre for the Study of Infectious and Tropical Diseases,b Department of Pharmaceutical Chemistry, Hebrew University School of Pharmacy, Jerusalem, Israelc Department of Molecular biology, Hebrew University — Hadassah Medical School, |
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Abstract: | Malaria parasites have been shown to be more susceptible to oxidative stress than their host erythro- cytes. In the present work, a chloroquine resistant malaria parasite, Plasmodium falciparum (FCR-3) was found to be susceptible in vitro to a pyridoxal based iron chelator — (l-[N-ethoxycarbonylmethyl- pyridoxlidenium]-2-[2'-pyridyl] hydrazine bromide — (code named L2-9). 2h exposure to 20μM L2-9 was sufficient to irreversibly inhibit parasite growth. Desferrioxamine blocked the drug effect, indicating the requirement for iron. Oxygen however, was not essential. Spectrophotometric analysis showed that under anoxic conditions, L2-9-Fe(II) chelate undergoes an intramolecular redox reaction which presumably involves a one electron transfer and is expected to result in the formation of free radical. Spin trapping coupled to electron spin resonance (ESR) studies of L2-9-iron chelate showed that L2-9-Fe(II) produced free radicals both in the presence and absence of cells, while L2-9-Fe(III) produced free radicals only in the presence of actively metabolising cells. |
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Keywords: | Red blood cells Plasmodium falciparum iron chelates free radicals electron spin resonance |
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