| Literature DB >> 33871252 |
Rubén Martín-Escolano1, Mikel Etxebeste-Mitxeltorena2,3,4, Javier Martín-Escolano5,6, Daniel Plano2,3,4, María J Rosales7, Socorro Espuelas2,3,4, Esther Moreno2,3,4, Manuel Sánchez-Moreno7, Carmen Sanmartín2,3,4, Clotilde Marín7.
Abstract
Chagas disease is a tropical infection caused by the protozoan parasite Trypanosoma cruzi and a global public health concern. It is a paradigmatic example of a chronic disease without an effective treatment. Current treatments targeting T. cruzi are limited to two obsolete nitroheterocyclic drugs, benznidazole and nifurtimox, which lead to serious drawbacks. Hence, new, more effective, safer, and affordable drugs are urgently needed. Selenium and their derivatives have emerged as an interesting strategy for the treatment of different prozotoan diseases, such as African trypanosomiasis, leishmaniasis, and malaria. In the case of Chagas disease, diverse selenium scaffolds have been reported with antichagasic activity in vitro and in vivo. On the basis of these premises, we describe the in vitro and in vivo trypanocidal activity of 41 selenocompounds against the three morphological forms of different T. cruzi strains. For the most active selenocompounds, their effect on the metabolic and mitochondrial levels and superoxide dismutase enzyme inhibition capacity were measured in order to determine the possible mechanism of action. Derivative 26, with a selenocyanate motif, fulfills the most stringent in vitro requirements for potential antichagasic agents and exhibits a better profile than benznidazole in vivo. This finding provides a step forward for the development of a new antichagasic agent.Entities:
Keywords: Chagas disease; Trypanosoma cruzi; chemotherapy; drug discovery; selenium derivatives
Year: 2021 PMID: 33871252 DOI: 10.1021/acsinfecdis.1c00048
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084