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Response to different benznidazole doses in animal models of chronic phase Chagas disease: a critical review
Scarim, Cauê Benito; Ribeiro, Aline Rimoldi; Rosa, João Aristeu da; Chin, Chung Man.
  • Scarim, Cauê Benito; Universidade Estadual Paulista Júlio de Mesquita Filho. Faculdade de Ciências Farmacêuticas. Departamento de Fármacos e Medicamentos. Araraquara. BR
  • Ribeiro, Aline Rimoldi; Universidade Estadual Paulista Júlio de Mesquita Filho. Faculdade de Ciências Farmacêuticas. Departamento de Fármacos e Medicamentos. Araraquara. BR
  • Rosa, João Aristeu da; Universidade Estadual Paulista Júlio de Mesquita Filho. Faculdade de Ciências Farmacêuticas. Departamento de Fármacos e Medicamentos. Araraquara. BR
  • Chin, Chung Man; Universidade Estadual Paulista Júlio de Mesquita Filho. Faculdade de Ciências Farmacêuticas. Departamento de Fármacos e Medicamentos. Araraquara. BR
Rev. Soc. Bras. Med. Trop ; 51(2): 133-140, Mar.-Apr. 2018. tab
Article in English | LILACS | ID: biblio-897057
ABSTRACT
Abstract Chagas disease is a protozoan infection that was identified over a century ago. No drugs are available to treat the indeterminate and determinate chronic phases of the disease. Success of a drug design is dependent on correct biological evaluation. Concerning new drug designs for Chagas disease, it is essential to first identify the most effective, existing, experimental chronic protocols that can be used for comparison purposes. Here, we present a literature review regarding experimental models with chronic Chagas disease to evaluate the efficacy of benznidazole (BZN). We searched literature published in PubMed and Web of Science databases, using these keywords animal model, BZN, Chagas disease, T. cruzi, and chronic phase, with no timeframe limitations. We excluded articles involving acute phase animal models and/or those without BZN treatment. The selected studies were conducted using different BZN concentrations (10mg-100mg) involving several different periods (5-70 days). Concentrations and durations of use are directly related to side effects, but do not prevent chronic tissue lesions. BZN use during the late/chronic phases of Chagas disease is unable to eliminate amastigote forms present in infected tissues. This study suggests the administration of a lower BZN concentration (<100mg/kg/day) during the chronic phase of the animal model, as this had been reported to result in fewer side effects.
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Full text: Available Index: LILACS (Americas) Main subject: Trypanocidal Agents / Chagas Disease / Dose-Response Relationship, Drug / Nitroimidazoles Type of study: Practice guideline Limits: Animals Language: English Journal: Rev. Soc. Bras. Med. Trop Journal subject: Tropical Medicine Year: 2018 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual Paulista Júlio de Mesquita Filho/BR

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Full text: Available Index: LILACS (Americas) Main subject: Trypanocidal Agents / Chagas Disease / Dose-Response Relationship, Drug / Nitroimidazoles Type of study: Practice guideline Limits: Animals Language: English Journal: Rev. Soc. Bras. Med. Trop Journal subject: Tropical Medicine Year: 2018 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual Paulista Júlio de Mesquita Filho/BR