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Verónica Galaz

Bio: Verónica Galaz is an academic researcher from University of Chile. The author has contributed to research in topics: Fumarate reductase & Reductase. The author has an hindex of 1, co-authored 1 publications receiving 51 citations.

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TL;DR: The data strongly suggest that trypanocidal action of the complexes could mainly rely on the inhibition of the parasite-specific enzyme NADH-fumarate reductase.
Abstract: In the search for new therapeutic tools against Chagas disease (American trypanosomiasis) palladium and platinum complexes of the bioactive ligand pyridine-2-thiol N-oxide were exhaustively characterized and evaluated in vitro. Both complexes showed high in vitro growth inhibition activity (IC(50) values in the nanomolar range) against Trypanosoma cruzi, the causative agent of the disease. They were 39-115 times more active than the antitrypanosomal drug Nifurtimox. The palladium complex showed an approximately threefold enhancement of the activity compared with the parent compound. In addition, owing to their low unspecific cytotoxicity on mammalian cells, the complexes showed a highly selective antiparasite activity. To get an insight into the mechanism of action of these compounds, DNA, redox metabolism (intraparasite free-radical production) and two parasite-specific enzymes absent in the host, namely, trypanothione reductase and NADH-fumarate reductase, were evaluated as potential parasite targets. Additionally, the effect of metal coordination on the free radical scavenger capacity previously reported for the free ligand was studied. All the data strongly suggest that trypanocidal action of the complexes could mainly rely on the inhibition of the parasite-specific enzyme NADH-fumarate reductase.

57 citations


Cited by
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TL;DR: This review focuses on recent advances in developing gold anti-parasitic agents and new uses of existing gold drugs against these old ailments, with emphasis on the major tropical diseases, malaria, leishmaniasis, trypanosomiasis and schistOSomiasis.

200 citations

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TL;DR: Recent progress in parasite genomics and the identification of a few biomolecular targets hold great promise for the discovery of new 'mechanism-based' antiparasitic metallodrugs.

191 citations

Journal ArticleDOI
TL;DR: A review of vanadium-based potential anti-parasitic agents, mainly active against the parasites causing American trypanosomiasis (Chagas disease), leishmaniasis and amoebiasis, is presented in this paper.

168 citations

Journal ArticleDOI
TL;DR: An overview of the most representative studies in the field with particular focus on the emerging protein targets – namely zinc-finger proteins, aquaglyceroporins, nitric oxide synthase, thymidine kinases and carbonic anhydrases – which have been also characterized for their interactions with metal-based compounds at a molecular level via different biophysical, analytical and computational methods.

123 citations