A Promising Amphotericin B Derivative Induces Morphological Alterations, Mitochondrial Damage, and Oxidative Stress In Vitro and Prevents Mice from Death Produced by a Virulent Strain of Trypanosoma cruzi


Por: Martínez, I, Rivera-Santiago, L, Rodríguez-Hernández, KD, Galván-Hernández, A, Rodríguez-Fragoso, L, Díaz-Peralta, L, Torres-Martínez, L, Agredano-Moreno, LT, Jiménez-García, LF, Ortega-Blake, I, Espinoza, B

Publicada: 1 jun 2024
Resumen:
Chagas Disease is a neglected tropical disease caused by the protozoan parasite Trypanosoma cruzi, affecting 6-8 million people, mainly in Latin America. The medical treatment is based on two compounds, benznidazole and nifurtimox, with limited effectiveness and that produce severe side effects; consequently, there is an urgent need to develop new, safe, and effective drugs. Amphotericin B is the most potent antimycotic known to date. A21 is a derivative of this compound with the property of binding to ergosterol present in cell membranes of some organisms. In the search for a new therapeutic drug against T. cruzi, the objective of this work was to study the in vitro and in vivo effects of A21 derivative on T. cruzi. Our results show that the A21 increased the reactive oxygen species and reduced the mitochondrial membrane potential, affecting the morphology, metabolism, and cell membrane permeability of T. cruzi in vitro. Even more important was finding that in an in vivo murine model of infection, A21 in combination with benznidazole was able to reduce blood parasitemia, diminish the immune inflammatory infiltrate in skeletal muscle and rescue all the mice from death due to a virulent T. cruzi strain.

Filiaciones:
Martínez, I:
 Univ Nacl Autonoma Mexico, Dept Inmunol, Lab Estudios Tripanosomiasis & Leishmaniasis, Inst Invest Biomed, Mexico City 04510, Afghanistan

Rivera-Santiago, L:
 Univ Nacl Autonoma Mexico, Dept Inmunol, Lab Estudios Tripanosomiasis & Leishmaniasis, Inst Invest Biomed, Mexico City 04510, Afghanistan

Rodríguez-Hernández, KD:
 Univ Nacl Autonoma Mexico, Dept Inmunol, Lab Estudios Tripanosomiasis & Leishmaniasis, Inst Invest Biomed, Mexico City 04510, Afghanistan

Galván-Hernández, A:
 Univ Nacl Autonoma Mexico, Inst Ciencias Fis, Apartado Postal 48-3, Cuernavaca 62251, Morelos, Mexico

Rodríguez-Fragoso, L:
 Univ Autonoma Estado Morelos, Fac Farm, Ave Univ 1001 Col,Chamilpa 62210, Cuernavaca, Morelos, Mexico

Díaz-Peralta, L:
 Univ Nacl Autonoma Mexico, Inst Ciencias Fis, Apartado Postal 48-3, Cuernavaca 62251, Morelos, Mexico

Torres-Martínez, L:
 Univ Nacl Autonoma Mexico, Dept Inmunol, Lab Estudios Tripanosomiasis & Leishmaniasis, Inst Invest Biomed, Mexico City 04510, Afghanistan

Agredano-Moreno, LT:
 Univ Nacl Autonoma Mexico, Fac Ciencias, Dept Biol Evolut, Mexico City 04510, Mexico

Jiménez-García, LF:
 Univ Nacl Autonoma Mexico, Fac Ciencias, Dept Biol Evolut, Mexico City 04510, Mexico

Ortega-Blake, I:
 Univ Nacl Autonoma Mexico, Inst Ciencias Fis, Apartado Postal 48-3, Cuernavaca 62251, Morelos, Mexico

Espinoza, B:
 Univ Nacl Autonoma Mexico, Dept Inmunol, Lab Estudios Tripanosomiasis & Leishmaniasis, Inst Invest Biomed, Mexico City 04510, Afghanistan
ISSN: 20762607
Editorial
MDPI, ST ALBAN-ANLAGE 66, CH-4052 BASEL, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 12 Número: 6
Páginas:
WOS Id: 001257566100001
ID de PubMed: 38930447
imagen gold, All Open Access; Gold Open Access