Literature DB >> 27216381

Novel cruzipain inhibitors for the chemotherapy of chronic Chagas disease.

María L Sbaraglini1, Carolina L Bellera2, Laura Fraccaroli3, Luciana Larocca3, Carolina Carrillo3, Alan Talevi2, Catalina D Alba Soto4.   

Abstract

Despite current efforts worldwide to develop new medications against Chagas disease, only two drugs are available, nifurtimox and benznidazole. Both drugs require prolonged treatment and have multiple side effects and limited efficacy on adult patients chronically infected with Trypanosoma cruzi. Recently, computer-guided drug repositioning led to the discovery of the trypanocidal effects of clofazimine and benidipine. These compounds showed inhibitory effects on cruzipain, the major cysteine protease of T. cruzi, of different parasite stages and in a murine model of acute Chagas disease. The aim of this work was to determine the efficacy of these novel cruzipain inhibitors when administered in a murine model of chronic Chagas disease. Benidipine and clofazimine were able to reduce the parasite burden in cardiac and skeletal muscles of chronically infected mice compared with untreated mice as well as diminish the inflammatory process in these tissues. Further studies should be performed to study the synergism with benznidazole and nifurtimox in view of combined therapies.
Copyright © 2016 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.

Entities:  

Keywords:  Benidipine; Chagas disease; Chronic phase; Clofazimine; Drug repositioning; Trypanosoma cruzi

Mesh:

Substances:

Year:  2016        PMID: 27216381     DOI: 10.1016/j.ijantimicag.2016.02.018

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  5 in total

Review 1.  Biological factors that impinge on Chagas disease drug development.

Authors:  Amanda F Francisco; Shiromani Jayawardhana; Michael D Lewis; Martin C Taylor; John M Kelly
Journal:  Parasitology       Date:  2017-08-23       Impact factor: 3.234

2.  Multi-Anti-Parasitic Activity of Arylidene Ketones and Thiazolidene Hydrazines against Trypanosoma cruzi and Leishmania spp.

Authors:  Guzmán Álvarez; Cintya Perdomo; Cathia Coronel; Elena Aguilera; Javier Varela; Gonzalo Aparicio; Flavio R Zolessi; Nallely Cabrera; Celeste Vega; Miriam Rolón; Antonieta Rojas de Arias; Ruy Pérez-Montfort; Hugo Cerecetto; Mercedes González
Journal:  Molecules       Date:  2017-05-07       Impact factor: 4.411

3.  Identification of clinically approved small molecules that inhibit growth and affect transcript levels of developmentally regulated genes in the African trypanosome.

Authors:  Madison Elle Walsh; Eleanor Mary Naudzius; Savanah Jessica Diaz; Theodore William Wismar; Mikhail Martchenko Shilman; Danae Schulz
Journal:  PLoS Negl Trop Dis       Date:  2020-03-13

4.  The Use of AlphaFold for In Silico Exploration of Drug Targets in the Parasite Trypanosoma cruzi.

Authors:  Albert Ros-Lucas; Nieves Martinez-Peinado; Jaume Bastida; Joaquim Gascón; Julio Alonso-Padilla
Journal:  Front Cell Infect Microbiol       Date:  2022-07-14       Impact factor: 6.073

5.  Crystal violet structural analogues identified by in silico drug repositioning present anti-Trypanosoma cruzi activity through inhibition of proline transporter TcAAAP069.

Authors:  Melisa Sayé; Lucrecia Gauna; Edward Valera-Vera; Chantal Reigada; Mariana R Miranda; Claudio A Pereira
Journal:  PLoS Negl Trop Dis       Date:  2020-01-21
  5 in total

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