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+54-11-528-58547

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Ciudad Universitaria

Pabellón II

8.30 a 16.00

Lunes a Viernes

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(+54 11) 4576-3346

info@qo.fcen.uba.ar

Ciudad Universitaria

Pabellón II

08:30 a 17:00 hs

Lunes a Viernes

Rodríguez, Juan Bautista

Doctor en Ciencias Químicas

Trypanosoma cruzi is the etiologic agent of American trypanosomiasis. The number of infected people with T. cruzi diminished from 18 million (1991) to 6 million (2010), but it is still the most the prevalent parasitic disease in the Americas. On the other hand, Toxoplasma gondii is an opportunistic Apicomplexan parasite responsible for toxoplasmosis, which is able to infect humans and warm-blooded animals affecting close to one billion people worldwide. The current chemotherapy for Chagas disease and toxoplasmosis is unsatisfactory and there is a critical need to develop new safe drugs. Our long-term goal is to find alternate drugs for the treatment of these parasitic diseases. Enzymes of isoprenoid pathway studied so far that are involved in the synthesis of sterols have been reported to be excellent drug targets against pathogenic parasites. For example, bisphosphonates have activity against T. cruzi targeting T. cruzi farnesyl diphosphate synthase (TcFPPS). T. gondii FPPS is a bifunctional enzyme that can catalyze the condensation of isopentenyl diphosphate with three allylic substrates forming not only 15-carbon FPP but also 20-carbon GGPP. T. cruzi squalene synthase (TcSQS) proved to be an interesting target for drug design. Aryloxyethyl thiocyanates are potent inhibitors of T. cruzi proliferation targeting TcSQS acting towards T. gondii as well. T. gondii does not synthesize cholesterol and imports it from the host suggesting that inhibitors of the host SQS could potentially affect T. gondii growth. Our hypothesis is that the isoprenoid pathway constitutes a major target for the treatment of parasitic diseases. To test this hypothesis, our specific aims are: to investigate the effect of bisphosphonates against TcFPPS and TgFPPS, and against T. cruzi and T. gondii cells, and perform SAR studies to assist drug design; to study the effect of aryloxyethyl thiocyanate derivatives against TcSQS, and also against T. cruzi and T. gondii cells.