Abstract

Combination therapy has gained attention as a possible strategy for overcoming the limitations of the present therapeutic arsenal for Chagas disease. The aim of this study was to evaluate the effect of allopurinol in association with nitroheterocyclic compounds on infection with the Y strain of Trypanosoma cruzi The in vitro effect of allopurinol plus benznidazole or nifurtimox on intracellular amastigotes in infected H9c2 cells was assessed in a 72-h assay. The interactions were classified as synergic for both allopurinol-nifurtimox (sums of fractional inhibitory concentrations [∑FICs] = 0.49 ± 0.08) and allopurinol-benznidazole (∑FICs = 0.48 ± 0.09). In the next step, infected Swiss mice were treated with allopurinol at 30, 60, and 90 mg/kg of body weight and with benznidazole at 25, 50, and 75 mg/kg in monotherapy and in combination at the same doses; as a reference treatment, another group of animals received benznidazole at 100 mg/kg. Allopurinol in monotherapy led to a smaller or nil effect in the reduction of parasite load and mortality rate. Treatment with benznidazole at suboptimal doses induced a transient suppression of parasitaemia with subsequent relapse in all animals treated with 25 and 50 mg/kg and in 80% of those that received 75 mg/kg. Administration of the drugs in combination significantly increased the cure rate to 60 to 100% among mice treated with benznidazole at 75 mg/kg plus 30, 60, or 90 mg/kg of allopurinol. These results show a positive interaction between allopurinol and benznidazole, and since both drugs are commercially available, their use in combination may be considered for the assessment in the treatment of Chagas disease patients.

Highlights

  • Combination therapy has gained attention as a possible strategy for overcoming the limitations of the present therapeutic arsenal for Chagas disease

  • The etiological treatment available for Chagas disease is based on nitroheterocyclic compounds and is effective in treating acute and early chronic phases, but it has less established efficacy when administered during the chronic phase of the disease [2]

  • Animals were treated during the chronic phase (3 months of infection) with 50 or 100 mg/kg of body weight of benznidazole administered for 30 consecutive days or intermittently with one treatment dose every 7 days (13 doses), associated or not with 64 mg/kg of allopurinol

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Summary

Introduction

Combination therapy has gained attention as a possible strategy for overcoming the limitations of the present therapeutic arsenal for Chagas disease. A number of studies have demonstrated the anti-T. cruzi activity of allopurinol: in vitro [20, 21], in murine models of acute infection [16, 18], and in the treatment of individuals in the chronic phase of Chagas disease from Chile and Argentina [22,23,24]. Allopurinol is not efficacious in the control of parasitemia of acute Chagas disease patients in monotherapy [26] or in curing patients in the chronic phase of Chagas disease from areas of endemicity in Brazil [27] These findings highlight the need to investigate alternative dosing regimens and possible combination therapies to improve the efficacy of allopurinol in treating Chagas disease. The objective of this study was to evaluate the effect of using allopurinol in combination with nitro compounds on in vitro and in vivo infection with T. cruzi

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