Literature DB >> 30625275

Successful Aspects of the Coadministration of Sterol 14α-Demethylase Inhibitor VFV and Benznidazole in Experimental Mouse Models of Chagas Disease Caused by the Drug-Resistant Strain of Trypanosoma cruzi.

Francisca Hildemagna Guedes-da-Silva, Denise da Gama Jaén Batista, Cristiane França Da Silva, Beatriz Philot Pavão, Marcos Meuser Batista, Otacílio Cruz Moreira, Letícia Rocha Quintino Souza, Constança Britto, Girish Rachakonda1, Fernando Villalta1, Galina I Lepesheva2, Maria de Nazaré Correia Soeiro.   

Abstract

Up to now, no vaccines are available for Chagas disease, and the current therapy is largely unsatisfactory. Novel imidazole-based scaffolds of protozoan sterol 14α-demethylase (CYP51) inhibitors have demonstrated potent antiparasitic activity with no acute toxicity. Presently our aim was to investigate the effectiveness of the experimental 14α-demethylase inhibitor VFV in the mouse models of Trypanosoma cruzi infection using a naturally drug-resistant Colombiana strain, under monotherapy and in association with the reference drug, benznidazole (Bz). The treatment with VFV resulted in complete parasitemia suppression and 100% animal survival when administered orally (given in 10% DMSO plus 5% Arabic gum) at 25 mg/kg (bid) for 60 days. However, as parasite relapse was found using VFV alone under this treatment scheme, the coadministration of VFV with Bz was assayed giving simultaneously (for 60 days, bid) by oral route, under two different drug vehicles (10% DMSO plus 5% Gum Arabic with or without 3% Tween 80). All tested mice groups resulted in >99.9% of parasitemia decrease and 100% animal survival. qPCR analysis performed on cyclophosphamide immunosuppressed mice revealed that, although presenting lack of cure, VFV given as monotherapy was 14-fold more active than Bz, and the coadministration of Bz plus VFV (given simultaneously, using 10% DMSO plus 5% Gum Arabic as vehicle) resulted in 106-fold lower blood parasitism as compared to the monotherapy of Bz. Another interesting finding was the parasitological cure in 70% of the animals treated with Bz and VFV when the coadministration was given using the VFV suspension in 10% DMSO + Arabic gum + Tween 80 (a formulation that we have found to provide a better pharmacokinetics), even after immunosuppression using cyclophosphamide cycles, supporting the promising aspect of the drug coadministration in improving the efficacy of therapeutic arsenal against T. cruzi.

Entities:  

Keywords:  Chagas disease; Colombiana strain; Trypanosoma cruzi; VFV; VNI; benznidazole; coadministration

Mesh:

Substances:

Year:  2019        PMID: 30625275      PMCID: PMC6408276          DOI: 10.1021/acsinfecdis.8b00253

Source DB:  PubMed          Journal:  ACS Infect Dis        ISSN: 2373-8227            Impact factor:   5.084


  38 in total

1.  Atovaquone and ELQ-300 Combination Therapy as a Novel Dual-Site Cytochrome bc1 Inhibition Strategy for Malaria.

Authors:  Allison M Stickles; Martin J Smilkstein; Joanne M Morrisey; Yuexin Li; Isaac P Forquer; Jane X Kelly; Sovitj Pou; Rolf W Winter; Aaron Nilsen; Akhil B Vaidya; Michael K Riscoe
Journal:  Antimicrob Agents Chemother       Date:  2016-07-22       Impact factor: 5.191

2.  In vitro and in vivo biological effects of novel arylimidamide derivatives against Trypanosoma cruzi.

Authors:  Bruno Lisboa Timm; Patrícia Bernadino da Silva; Marcos Meuser Batista; Francisca Hildemagna Guedes da Silva; Cristiane França da Silva; Richard R Tidwell; Donald A Patrick; Susan Kilgore Jones; Stanislav A Bakunov; Svetlana M Bakunova; Maria de Nazaré C Soeiro
Journal:  Antimicrob Agents Chemother       Date:  2014-04-21       Impact factor: 5.191

Review 3.  Sterol 14alpha-demethylase (CYP51) as a therapeutic target for human trypanosomiasis and leishmaniasis.

Authors:  Galina I Lepesheva; Michael R Waterman
Journal:  Curr Top Med Chem       Date:  2011       Impact factor: 3.295

4.  The Investigational Fungal Cyp51 Inhibitor VT-1129 Demonstrates Potent In Vitro Activity against Cryptococcus neoformans and Cryptococcus gattii.

Authors:  Shawn R Lockhart; Annette W Fothergill; Naureen Iqbal; Carol B Bolden; Nina T Grossman; Edward P Garvey; Stephen R Brand; William J Hoekstra; Robert J Schotzinger; Elizabeth Ottinger; Thomas F Patterson; Nathan P Wiederhold
Journal:  Antimicrob Agents Chemother       Date:  2016-03-25       Impact factor: 5.191

5.  In vitro trypanocidal activity of DB745B and other novel arylimidamides against Trypanosoma cruzi.

Authors:  Cristiane França Da Silva; Angela Junqueira; Marli Maria Lima; Alvaro José Romanha; Policarpo Ademar Sales Junior; Chad E Stephens; Phanneth Som; David W Boykin; Maria de Nazaré Correia Soeiro
Journal:  J Antimicrob Chemother       Date:  2011-04-08       Impact factor: 5.790

6.  Elimination of Chagas disease transmission: perspectives.

Authors:  João Carlos Pinto Dias
Journal:  Mem Inst Oswaldo Cruz       Date:  2009-07       Impact factor: 2.743

7.  Different Therapeutic Outcomes of Benznidazole and VNI Treatments in Different Genders in Mouse Experimental Models of Trypanosoma cruzi Infection.

Authors:  F H Guedes-da-Silva; D G J Batista; C F da Silva; M B Meuser; M R Simões-Silva; J S de Araújo; C G Ferreira; O C Moreira; C Britto; G I Lepesheva; Maria de Nazaré C Soeiro
Journal:  Antimicrob Agents Chemother       Date:  2015-09-28       Impact factor: 5.191

8.  Limited Ability of Posaconazole To Cure both Acute and Chronic Trypanosoma cruzi Infections Revealed by Highly Sensitive In Vivo Imaging.

Authors:  Amanda Fortes Francisco; Michael D Lewis; Shiromani Jayawardhana; Martin C Taylor; Eric Chatelain; John M Kelly
Journal:  Antimicrob Agents Chemother       Date:  2015-05-26       Impact factor: 5.191

9.  Assessing anti-T. cruzi candidates in vitro for sterile cidality.

Authors:  Monica Cal; Jean-Robert Ioset; Matthia A Fügi; Pascal Mäser; Marcel Kaiser
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2016-08-26       Impact factor: 4.077

10.  Nitroheterocyclic compounds are more efficacious than CYP51 inhibitors against Trypanosoma cruzi: implications for Chagas disease drug discovery and development.

Authors:  Carolina B Moraes; Miriam A Giardini; Hwayoung Kim; Caio H Franco; Adalberto M Araujo-Junior; Sergio Schenkman; Eric Chatelain; Lucio H Freitas-Junior
Journal:  Sci Rep       Date:  2014-04-16       Impact factor: 4.379

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  4 in total

1.  Combination Therapy Using Benznidazole and Aspirin during the Acute Phase of Experimental Chagas Disease Prevents Cardiovascular Dysfunction and Decreases Typical Cardiac Lesions in the Chronic Phase.

Authors:  Rito Santo Pereira; Aparecida Donizette Malvezi; Maria Isabel Lovo-Martins; Bruno Fernando Cruz Lucchetti; Jussevania Pereira Santos; Eliandro Reis Tavares; Waldiceu Aparecido Verri; Eduardo José de Almeida Araújo; Lucy Megumi Yamauchi; Sueli Fumie Yamada-Ogatta; Marli Cardoso Martins-Pinge; Phileno Pinge-Filho
Journal:  Antimicrob Agents Chemother       Date:  2020-06-23       Impact factor: 5.191

Review 2.  Advances in preclinical approaches to Chagas disease drug discovery.

Authors:  Fernando Villalta; Girish Rachakonda
Journal:  Expert Opin Drug Discov       Date:  2019-08-14       Impact factor: 6.098

3.  7-Aryl-7-deazapurine 3'-deoxyribonucleoside derivative as a novel lead for Chagas' disease therapy: in vitro and in vivo pharmacology.

Authors:  Camila Cardoso-Santos; Ludmila Ferreira de Almeida Fiuza; Cristiane França da Silva; Ana Lia Mazzeti; Roberson Donola Girão; Gabriel Melo de Oliveira; Denise da Gama Jaen Batista; Otacilio Cruz Moreira; Natália Lins da Silva Gomes; Louis Maes; Guy Caljon; Fabian Hulpia; Serge V Calenbergh; Maria de Nazaré Correia Soeiro
Journal:  JAC Antimicrob Resist       Date:  2021-11-17

4.  Perspectives for a new drug candidate for Chagas disease therapy.

Authors:  Maria de Nazaré Correia Soeiro
Journal:  Mem Inst Oswaldo Cruz       Date:  2022-03-14       Impact factor: 2.743

  4 in total

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