Identification of Aryl Polyamines Derivatives as Anti-Trypanosoma cruzi Agents Targeting Iron Superoxide Dismutase

Author:

Martín-Escolano RubénORCID,Molina-Carreño Daniel,Martín-Escolano Javier,Clares Mª Paz,Galiana-Roselló CristinaORCID,González-García JorgeORCID,Cirauqui Nuria,Llinares José M.,Rosales María José,García-España Enrique,Marín ClotildeORCID

Abstract

Chagas disease (CD) is a tropical and potentially fatal infection caused by Trypanosoma cruzi. Although CD was limited to Latin America as a silent disease, CD has become widespread as a result of globalization. Currently, 6–8 million people are infected worldwide, and no effective treatment is available. Here, we identify new effective agents against T. cruzi. In short, 16 aryl polyamines were screened in vitro against different T. cruzi strains, and lead compounds were evaluated in vivo after oral administration in both the acute and chronic infections. The mode of action was also evaluated at the energetic level, and its high activity profile could be ascribed to a mitochondria-dependent bioenergetic collapse and redox stress by inhibition of the Fe-SOD enzyme. We present compound 15 as a potential compound that provides a step forward for the development of new agents to combat CD.

Funder

Ministerio de Economia, Industria y Competitividad

MINECO and FEDER funds

Alfonso Martín Escudero Foundation

Publisher

MDPI AG

Subject

Pharmaceutical Science

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