Literature DB >> 25733492

Trypanothione reductase inhibitors: Overview of the action of thioridazine in different stages of Chagas disease.

M Silvina Lo Presti1, P Carolina Bazán2, Mariana Strauss2, Alejandra L Báez2, H Walter Rivarola2, Patricia A Paglini-Oliva2.   

Abstract

Thioridazine (TDZ) is a phenothiazine that has been shown to be one of the most potent phenothiazines to inhibit trypanothione reductase irreversibly. Trypanothione reductase is an essential enzyme for the survival of Trypanosoma cruzi in the host. Here, we reviewed the use of this drug for the treatment of T. cruzi experimental infection. In our laboratory, we have studied the effect of TDZ for the treatment of mice infected with different strains of T. cruzi and treated in the acute or in the chronic phases of the experimental infection, using two different schedules: TDZ at a dose of 80 mg/kg/day, for 3 days starting 1h after infection (acute phase), or TDZ 80 mg/kg/day for 12 days starting 180 days post infection (d.p.i.) (chronic phase). In our experience, the treatment of infected mice, in the acute or in the chronic phases of the infection, with TDZ led to a large reduction in the mortality rates and in the cardiac histological and electrocardiographical abnormalities, and modified the natural evolution of the experimental infection. These analyses reinforce the importance of treatment in the chronic phase to decrease, retard or stop the evolution to chagasic myocardiopathy. Other evidence leading to the use of this drug as a potential chemotherapeutic agent for Chagas disease treatment is also revised.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chagas disease chemotherapy; Thioridazine; Trypanosoma cruzi strains; Trypanotione reductase

Mesh:

Substances:

Year:  2015        PMID: 25733492     DOI: 10.1016/j.actatropica.2015.02.012

Source DB:  PubMed          Journal:  Acta Trop        ISSN: 0001-706X            Impact factor:   3.112


  6 in total

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Journal:  Antimicrob Agents Chemother       Date:  2016-05-23       Impact factor: 5.191

Review 2.  Challenges in the chemotherapy of Chagas disease: Looking for possibilities related to the differences and similarities between the parasite and host.

Authors:  Vitor Sueth-Santiago; Debora Decote-Ricardo; Alexandre Morrot; Celio Geraldo Freire-de-Lima; Marco Edilson Freire Lima
Journal:  World J Biol Chem       Date:  2017-02-26

3.  Relevance of Trypanothione Reductase Inhibitors on Trypanosoma cruzi Infection: A Systematic Review, Meta-Analysis, and In Silico Integrated Approach.

Authors:  Andréa Aparecida Santos Mendonça; Camila Morais Coelho; Marcia Paranho Veloso; Ivo Santana Caldas; Reggiani Vilela Gonçalves; Antônio Lucio Teixeira; Aline Silva de Miranda; Rômulo Dias Novaes
Journal:  Oxid Med Cell Longev       Date:  2018-10-24       Impact factor: 6.543

4.  Design, Synthesis, and Structural Characterization of Novel Diazaphenothiazines with 1,2,3-Triazole Substituents as Promising Antiproliferative Agents.

Authors:  Beata Morak-Młodawska; Krystian Pluta; Małgorzata Latocha; Małgorzata Jeleń; Dariusz Kuśmierz
Journal:  Molecules       Date:  2019-11-30       Impact factor: 4.411

5.  Repositioned Drugs for Chagas Disease Unveiled via Structure-Based Drug Repositioning.

Authors:  Melissa F Adasme; Sarah Naomi Bolz; Lauren Adelmann; Sebastian Salentin; V Joachim Haupt; Adriana Moreno-Rodríguez; Benjamín Nogueda-Torres; Verónica Castillo-Campos; Lilián Yepez-Mulia; José A De Fuentes-Vicente; Gildardo Rivera; Michael Schroeder
Journal:  Int J Mol Sci       Date:  2020-11-20       Impact factor: 5.923

6.  Antioxidant effect of Morus nigra on Chagas disease progression.

Authors:  Michelly Cristina Montenote; Vithor Zuccaro Wajsman; Yoichi Takaki Konno; Paulo César Ferreira; Regildo Márcio Gonçalves Silva; Altino Luiz Silva Therezo; Luciana Pereira Silva; Luciamáre Perinetti Alves Martins
Journal:  Rev Inst Med Trop Sao Paulo       Date:  2017-11-06       Impact factor: 1.846

  6 in total

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